[X] Close
You are about to erase all the values you have customized, search history, page format, etc.
Click here to RESET all values       Click here to GO BACK without resetting any value
Items 1 to 100 of about 535
1. Sevinc C, Akpinar H, Tufek I, Obek C, Kural AR: Radical retropubic prostatectomy as a solo therapy for treatment of adult rhabdomyosarcoma. Urol J; 2008;5(3):203-5
MedlinePlus Health Information. consumer health - Prostate Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Radical retropubic prostatectomy as a solo therapy for treatment of adult rhabdomyosarcoma.
  • [MeSH-major] Prostatectomy. Prostatic Neoplasms / surgery. Rhabdomyosarcoma, Embryonal / surgery

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18825631.001).
  • [ISSN] 1735-546X
  • [Journal-full-title] Urology journal
  • [ISO-abbreviation] Urol J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Iran
  •  go-up   go-down


2. Wu TH, Huang JS, Wang HM, Wang CH, Yeh KY: Long-term survivors of adult rhabdomyosarcoma of maxillary sinus following multimodal therapy: case reports and literature reviews. Chang Gung Med J; 2010 Jul-Aug;33(4):466-71

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Long-term survivors of adult rhabdomyosarcoma of maxillary sinus following multimodal therapy: case reports and literature reviews.
  • Rhabdomyosarcoma of the maxillary sinus is uncommon in adults.
  • This article describes two adult patients with rhabdomyosarcoma of the maxillary sinus who achieved long-term survival after undergoing multimodal therapy.
  • We also reviewed the literature regarding 23 patients who were 15 years of age or older and had rhabdomyosarcoma of the maxillary sinus and were treated between 1950 and 2000.
  • Results of our analysis suggest that multimodal therapy may become the mainstay treatment for adult rhabdomyosarcoma of the maxillary sinus.
  • [MeSH-major] Maxillary Sinus Neoplasms / therapy. Rhabdomyosarcoma / therapy
  • [MeSH-minor] Adolescent. Adult. Combined Modality Therapy. Female. Humans. Neoplasm Staging. Survivors

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20804675.001).
  • [ISSN] 2309-835X
  • [Journal-full-title] Chang Gung medical journal
  • [ISO-abbreviation] Chang Gung Med J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] China (Republic : 1949- )
  •  go-up   go-down


3. Van Rijn RR, Wilde JC, Bras J, Oldenburger F, McHugh KM, Merks JH: Imaging findings in noncraniofacial childhood rhabdomyosarcoma. Pediatr Radiol; 2008 Jun;38(6):617-34
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Imaging findings in noncraniofacial childhood rhabdomyosarcoma.
  • Rhabdomyosarcoma (RMS) is the most common soft-tissue sarcoma of childhood.
  • [MeSH-major] Magnetic Resonance Imaging / methods. Muscle Neoplasms / diagnosis. Radiography / methods. Rhabdomyosarcoma / diagnosis. Thoracic Neoplasms / diagnosis. Ultrasonography / methods. Urogenital Neoplasms / diagnosis
  • [MeSH-minor] Adult. Child. Humans. Positron-Emission Tomography / methods. Tomography, X-Ray Computed / methods

  • MedlinePlus Health Information. consumer health - MRI Scans.
  • MedlinePlus Health Information. consumer health - Ultrasound.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] J Clin Oncol. 2004 Dec 1;22(23):4787-94 [15570080.001]
  • [Cites] Lancet Oncol. 2005 Feb;6(2):77-84 [15683816.001]
  • [Cites] AJR Am J Roentgenol. 2005 Apr;184(4):1293-304 [15788613.001]
  • [Cites] Int J Radiat Oncol Biol Phys. 2005 Apr 1;61(5):1432-8 [15817347.001]
  • [Cites] J Clin Oncol. 2005 Apr 20;23(12):2586-7 [15728222.001]
  • [Cites] J Clin Oncol. 2005 Apr 20;23(12):2618-28 [15728225.001]
  • [Cites] J Clin Oncol. 2005 Jul 1;23(19):4363-71 [15994146.001]
  • [Cites] Pediatr Radiol. 2005 Aug;35(8):766-73 [15864576.001]
  • [Cites] Pediatr Hematol Oncol. 2005 Sep;22(6):525-9 [16169819.001]
  • [Cites] J Clin Oncol. 2005 Oct 1;23(28):7143-51 [16192598.001]
  • [Cites] Pediatr Blood Cancer. 2006 Feb;46(2):127-34 [16231313.001]
  • [Cites] Pediatr Surg Int. 2006 Feb;22(2):135-9 [16328338.001]
  • [Cites] Pediatr Radiol. 2006 May;36(5):426-31 [16532346.001]
  • [Cites] Acta Orthop Belg. 2006 Apr;72(2):199-203 [16768266.001]
  • [Cites] Clin Nucl Med. 2006 Jul;31(7):394-7 [16785806.001]
  • [Cites] J Pediatr Hematol Oncol. 2006 Jul;28(7):440-5 [16825990.001]
  • [Cites] J Clin Oncol. 2006 Sep 20;24(27):4492-8 [16983119.001]
  • [Cites] J Urol. 2006 Nov;176(5):2190-4; discussion 2194-5 [17070290.001]
  • [Cites] Arch Pathol Lab Med. 2006 Oct;130(10):1454-65 [17090187.001]
  • [Cites] J Pediatr Adolesc Gynecol. 2000 May;13(2):75-8 [10869967.001]
  • [Cites] Med Pediatr Oncol. 2000 Aug;35(2):104-9 [10918231.001]
  • [Cites] Med Pediatr Oncol. 2000 Aug;35(2):147-9 [10918244.001]
  • [Cites] Cancer. 2000 Oct 15;89(8):1726-31 [11042567.001]
  • [Cites] J Pediatr Hematol Oncol. 2000 Nov-Dec;22(6):510-4 [11132218.001]
  • [Cites] J Clin Oncol. 2001 Jan 1;19(1):197-204 [11134213.001]
  • [Cites] AJR Am J Roentgenol. 2001 Feb;176(2):289-96 [11159059.001]
  • [Cites] AJR Am J Roentgenol. 2001 Feb;176(2):297-301 [11159060.001]
  • [Cites] Cancer. 2001 Feb 1;91(3):606-12 [11169945.001]
  • [Cites] Clin Imaging. 2000 Sep-Oct;24(5):257-62 [11331151.001]
  • [Cites] J Clin Oncol. 2001 Jun 15;19(12):3091-102 [11408506.001]
  • [Cites] AJR Am J Roentgenol. 2001 Jul;177(1):229-36 [11418435.001]
  • [Cites] J Pediatr Surg. 2001 Jul;36(7):1062-5 [11431779.001]
  • [Cites] J Pediatr Surg. 2001 Dec;36(12):1796-801 [11733909.001]
  • [Cites] Med Pediatr Oncol. 2002 Feb;38(2):146 [11813191.001]
  • [Cites] J Pediatr Surg. 2002 Apr;37(4):576-81 [11912514.001]
  • [Cites] Rev Hosp Clin Fac Med Sao Paulo. 2002 Mar-Apr;57(2):67-72 [11981587.001]
  • [Cites] J Clin Oncol. 2002 Jun 1;20(11):2672-9 [12039929.001]
  • [Cites] Am J Surg Pathol. 2002 Sep;26(9):1175-83 [12218574.001]
  • [Cites] Paediatr Respir Rev. 2002 Dec;3(4):328-38 [12457604.001]
  • [Cites] J Clin Oncol. 2003 Jan 1;21(1):78-84 [12506174.001]
  • [Cites] J Clin Oncol. 2003 Mar 1;21(5):793-8 [12610176.001]
  • [Cites] J Urol. 2003 Apr;169(4):1495-6 [12629400.001]
  • [Cites] J Pediatr Surg. 2003 Apr;38(4):548-52 [12677563.001]
  • [Cites] J Pediatr Adolesc Gynecol. 2003 Jun;16(3):139-42 [12804937.001]
  • [Cites] Urol Int. 2003;71(1):114-7 [12845275.001]
  • [Cites] Eur J Cancer. 2003 Jul;39(11):1594-602 [12855267.001]
  • [Cites] Pediatr Dermatol. 2003 Jul-Aug;20(4):335-8 [12869157.001]
  • [Cites] Cancer. 2003 Aug 1;98(3):571-80 [12879475.001]
  • [Cites] Cardiovasc Pathol. 2003 Sep-Oct;12(5):267-70 [14507576.001]
  • [Cites] Med Pediatr Oncol. 2003 Dec;41(6):584-7 [14595726.001]
  • [Cites] Clin Orthop Relat Res. 2003 Oct;(415):4-18 [14612624.001]
  • [Cites] Pediatr Radiol. 2003 Nov;33(11):739-43 [14655676.001]
  • [Cites] J Clin Oncol. 2004 Jan 1;22(1):143-9 [14701776.001]
  • [Cites] Br J Radiol. 2004 Feb;77(914):159-60 [15010393.001]
  • [Cites] Am J Surg Pathol. 1993 May;17(5):443-53 [8470759.001]
  • [Cites] Med Pediatr Oncol. 1994;22(1):15-21 [8232075.001]
  • [Cites] Radiology. 1994 Jan;190(1):263-8 [8259417.001]
  • [Cites] Cancer. 1994 Apr 1;73(7):1984-6 [8137226.001]
  • [Cites] Paediatr Perinat Epidemiol. 1994 Jan;8(1):107-19 [8153013.001]
  • [Cites] Cancer. 1995 Jan 1;75(1 Suppl):395-405 [8001010.001]
  • [Cites] J Clin Oncol. 1995 Mar;13(3):610-30 [7884423.001]
  • [Cites] Ann Urol (Paris). 1994;28(6-7):302-5 [7893115.001]
  • [Cites] Cancer. 1995 Sep 15;76(6):1073-85 [8625211.001]
  • [Cites] Cancer. 1995 Nov 15;76(10):1860-7 [8625059.001]
  • [Cites] J Clin Oncol. 1997 Jan;15(1):69-75 [8996126.001]
  • [Cites] Radiographics. 1997 Jul-Aug;17(4):919-37 [9225391.001]
  • [Cites] J Pediatr Surg. 1997 Sep;32(9):1381-3 [9314270.001]
  • [Cites] Cancer. 1997 Oct 15;80(8):1513-7 [9338477.001]
  • [Cites] Radiol Clin North Am. 1997 Nov;35(6):1265-80 [9374990.001]
  • [Cites] Pediatr Pulmonol. 1998 Jan;25(1):62-6 [9475333.001]
  • [Cites] Pediatr Radiol. 1998 Feb;28(2):101-8 [9472056.001]
  • [Cites] Ann Surg. 1998 Feb;227(2):170-3 [9488512.001]
  • [Cites] AJR Am J Roentgenol. 1998 May;170(5):1385-7 [9574621.001]
  • [Cites] Clin Radiol. 1999 Jan;54(1):2-10 [9915504.001]
  • [Cites] Acta Cytol. 1997 Jul-Aug;41(4 Suppl):1293-8 [9990261.001]
  • [Cites] Am J Surg Pathol. 1999 Mar;23(3):249-56 [10078913.001]
  • [Cites] Pediatr Blood Cancer. 2007 Mar;48(3):370-1 [16856157.001]
  • [Cites] Int J Radiat Oncol Biol Phys. 2007 Feb 1;67(2):497-504 [17084557.001]
  • [Cites] Ann Thorac Surg. 2007 Feb;83(2):687-9 [17258019.001]
  • [Cites] Curr Opin Oncol. 2007 May;19(3):248-53 [17414644.001]
  • [Cites] JAMA. 2007 Jun 27;297(24):2705-15 [17595271.001]
  • [Cites] AJR Am J Roentgenol. 2007 Aug;189(2):371-7 [17646463.001]
  • [Cites] Diagn Cytopathol. 2007 Aug;35(8):482-7 [17636492.001]
  • [Cites] Lancet Oncol. 2007 Aug;8(8):725-9 [17679082.001]
  • [Cites] Semin Nucl Med. 2007 Sep;37(5):316-31 [17707239.001]
  • [Cites] Genes Chromosomes Cancer. 1999 Dec;26(4):275-85 [10534762.001]
  • [Cites] J Clin Oncol. 1999 Nov;17(11):3468-75 [10550144.001]
  • [Cites] J Clin Oncol. 1999 Nov;17(11):3487-93 [10550146.001]
  • [Cites] Pediatr Radiol. 1999 Nov;29(11):823-5 [10552061.001]
  • [Cites] J Clin Oncol. 1999 Jul;17(7):2117-22 [10561266.001]
  • [Cites] J Clin Oncol. 1999 Dec;17(12):3706-19 [10577842.001]
  • [Cites] Br J Plast Surg. 1999 Jun;52(4):304-7 [10624299.001]
  • [Cites] J Natl Cancer Inst. 2000 Feb 2;92(3):205-16 [10655437.001]
  • [Cites] Int J Radiat Oncol Biol Phys. 2000 Jan 15;46(2):427-32 [10661350.001]
  • [Cites] J Pediatr Surg. 2000 Feb;35(2):309-16 [10693686.001]
  • [Cites] Pediatr Radiol. 2007 Nov;37(11):1179 [17690877.001]
  • [Cites] Br J Radiol. 2004 Mar;77(915):250-2 [15020370.001]
  • [Cites] Int J Radiat Oncol Biol Phys. 2004 Sep 1;60(1):265-74 [15337565.001]
  • [Cites] Pediatr Dev Pathol. 2004 Jul-Aug;7(4):361-9 [15383931.001]
  • [Cites] J Pediatr Surg. 1981 Dec;16(6):828-34 [7338762.001]
  • [Cites] Radiother Oncol. 1985 Apr;3(3):227-36 [3890032.001]
  • [Cites] Gynecol Oncol. 1986 Oct;25(2):171-94 [3758828.001]
  • [Cites] Cancer. 1988 Jan 15;61(2):209-20 [3275486.001]
  • [Cites] Histopathology. 1989 Sep;15(3):309-11 [2807189.001]
  • [Cites] J Clin Oncol. 1990 Nov;8(11):1847-53 [2230871.001]
  • [Cites] J Pediatr Surg. 1990 Dec;25(12):1256-8 [2286899.001]
  • [Cites] Am J Surg Pathol. 1991 Mar;15(3):257-67 [1847608.001]
  • [Cites] Am J Surg Pathol. 1992 Mar;16(3):229-35 [1599014.001]
  • [Cites] Am J Surg Pathol. 1993 Mar;17(3):221-30 [8434703.001]
  • [Cites] Cancer. 1993 Mar 1;71(5):1904-22 [8448756.001]
  • (PMID = 18324394.001).
  • [ISSN] 0301-0449
  • [Journal-full-title] Pediatric radiology
  • [ISO-abbreviation] Pediatr Radiol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 114
  • [Other-IDs] NLM/ PMC2367394
  •  go-up   go-down


Advertisement
4. Allen SD, Moskovic EC, Fisher C, Thomas JM: Adult rhabdomyosarcoma: cross-sectional imaging findings including histopathologic correlation. AJR Am J Roentgenol; 2007 Aug;189(2):371-7
The Lens. Cited by Patents in .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult rhabdomyosarcoma: cross-sectional imaging findings including histopathologic correlation.
  • OBJECTIVE: The purpose of our study was to present the MRI and CT features of adult rhabdomyosarcomas with histopathologic correlation.
  • Forty-nine sequential cases were incorporated over a 5-year period from the sarcoma unit database.
  • CONCLUSION: Although adult rhabdomyosarcomas have certain imaging appearances in common with other soft-tissue sarcomas, features at presentation such as tumor heterogeneity, site, regional lymphadenopathy, and pulmonary metastasis should make the radiologist consider this important diagnosis.
  • [MeSH-major] Rhabdomyosarcoma / diagnosis
  • [MeSH-minor] Adult. Contrast Media. Diagnosis, Differential. Female. Gadolinium DTPA. Humans. Magnetic Resonance Imaging / methods. Male. Middle Aged. Tomography, X-Ray Computed

  • Hazardous Substances Data Bank. GADOPENTETATE DIMEGLUMINE .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17646463.001).
  • [ISSN] 1546-3141
  • [Journal-full-title] AJR. American journal of roentgenology
  • [ISO-abbreviation] AJR Am J Roentgenol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Contrast Media; K2I13DR72L / Gadolinium DTPA
  •  go-up   go-down


5. Rohaizam J, Doris EJ, Tang PI, Lee SC, Uchang J: Adult embryonal rhabdomyosarcoma of the ethmoid: a rare entity. Med J Malaysia; 2010 Jun;65(2):160-1
Genetic Alliance. consumer health - Rhabdomyosarcoma embryonal.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult embryonal rhabdomyosarcoma of the ethmoid: a rare entity.
  • Embryonal rhabdomyosarcoma is an exceedingly rare tumor in adult.
  • We report an embryonal rhabdomyosarcoma of the ethmoid in a 59-year-old Iban lady who presented with proptosis and complete ptosis of her left eye for two months.
  • [MeSH-major] Exophthalmos. Rhabdomyosarcoma, Embryonal
  • [MeSH-minor] Adult. Humans. Orbital Neoplasms

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 23756807.001).
  • [ISSN] 0300-5283
  • [Journal-full-title] The Medical journal of Malaysia
  • [ISO-abbreviation] Med. J. Malaysia
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Malaysia
  •  go-up   go-down


6. Ogilvie CM, Crawford EA, Slotcavage RL, King JJ, Lackman RD, Hartner L, Staddon AP: Treatment of adult rhabdomyosarcoma. Am J Clin Oncol; 2010 Apr;33(2):128-31
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Treatment of adult rhabdomyosarcoma.
  • OBJECTIVES: Rhabdomyosarcoma is an exceedingly rare tumor in adults, and standard chemotherapy used for children is much less effective in adults.
  • This study examines short-term outcomes using doxorubicin, ifosfamide, and vincristine for adult rhabdomyosarcoma.
  • METHODS: Pathology records were searched for adults (age, >18) with rhabdomyosarcoma treated at our musculoskeletal tumor center.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Rhabdomyosarcoma / therapy
  • [MeSH-minor] Adult. Aged. Combined Modality Therapy. Doxorubicin / administration & dosage. Female. Follow-Up Studies. Humans. Ifosfamide / administration & dosage. Male. Middle Aged. Radiotherapy Dosage. Survival Rate. Treatment Outcome. Vincristine / administration & dosage. Young Adult

  • Hazardous Substances Data Bank. DOXORUBICIN .
  • Hazardous Substances Data Bank. IFOSFAMIDE .
  • Hazardous Substances Data Bank. VINCRISTINE .
  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19770626.001).
  • [ISSN] 1537-453X
  • [Journal-full-title] American journal of clinical oncology
  • [ISO-abbreviation] Am. J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 5J49Q6B70F / Vincristine; 80168379AG / Doxorubicin; UM20QQM95Y / Ifosfamide
  •  go-up   go-down


7. Chatterjee JS, Powell AP, Chatterjee D: Pleomorphic rhabdomyosarcoma of the diaphragm. J Natl Med Assoc; 2005 Jan;97(1):95-8
The Weizmann Institute of Science GeneCards and MalaCards databases. gene/protein/disease-specific - MalaCards for pleomorphic rhabdomyosarcoma .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Pleomorphic rhabdomyosarcoma of the diaphragm.
  • Pleomorphic rhabdomyosarcoma of the diaphragm represents fewer than 0.0001% of all cancers.
  • It is an adult disease of both sexes, the lowest reported age being 14 years.
  • [MeSH-major] Diaphragm. Muscle Neoplasms. Rhabdomyosarcoma
  • [MeSH-minor] Adult. Humans. Male

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Cancer. 1958 Jan-Feb;11(1):1-3 [13500286.001]
  • [Cites] Surgery. 1952 Dec;32(6):1023-64 [13005336.001]
  • [Cites] J Bone Joint Surg Am. 1965 Jun;47:715-26 [14299664.001]
  • [Cites] J Pediatr. 1959 Nov;55:620-34 [13803494.001]
  • [Cites] Rev Hosp Clin Fac Med Sao Paulo. 2002 Mar-Apr;57(2):67-72 [11981587.001]
  • [Cites] Cancer. 1968 Nov;22(5):956-67 [5686645.001]
  • [Cites] Am J Gastroenterol. 1971 Dec;56(6):555-8 [5134884.001]
  • [Cites] Pathol Annu. 1972;7:81-106 [4557937.001]
  • [Cites] Indian J Cancer. 1972 Mar;9(1):42-9 [5044708.001]
  • [Cites] Ann Med Interne (Paris). 1972 Feb;123(2):181-5 [5055075.001]
  • [Cites] Wien Z Inn Med. 1973;54(2):78-84 [4588077.001]
  • [Cites] Cancer. 1975 Aug;36(2):759-64 [1157035.001]
  • [Cites] Tumori. 1975 Mar-Apr;61(2):129-50 [1226574.001]
  • [Cites] J Natl Med Assoc. 1988 Feb;80(2):214-7 [3071608.001]
  • [Cites] Am J Surg Pathol. 1998 Apr;22(4):459-64 [9537474.001]
  • [Cites] Surgery. 1962 Oct;52:572-84 [14484432.001]
  • (PMID = 15719879.001).
  • [ISSN] 1943-4693
  • [Journal-full-title] Journal of the National Medical Association
  • [ISO-abbreviation] J Natl Med Assoc
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] United States
  • [Number-of-references] 29
  • [Other-IDs] NLM/ PMC2568583
  •  go-up   go-down


8. Muto E, Shioyama Y, Nakamura K, Ohga' S, Nomoto S, Toba T, Yoshitake T, Soeda H, Terashima H, Honda H: Adult rhabdomyosarcoma in the nasal and paranasal sinuses showing complete local response to a combination of chemotherapy and radiotherapy using 3D-CRT and IMRT. Fukuoka Igaku Zasshi; 2005 Oct;96(10):363-9
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult rhabdomyosarcoma in the nasal and paranasal sinuses showing complete local response to a combination of chemotherapy and radiotherapy using 3D-CRT and IMRT.
  • We report on a 69-year-old woman with rhabdomyosarcoma arising from the nasal and paranasal sinuses.
  • A biopsy specimen from the nasal tumor was diagnosed histologically as a rhabdomyosarcoma, alveolar type.
  • Chemoradiotherapy may be an effective treatment also for inoperable adult rhabdomyosarcoma in the head and neck region.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Paranasal Sinus Neoplasms / therapy. Radiotherapy, Conformal / methods. Radiotherapy, Intensity-Modulated / methods. Rhabdomyosarcoma / therapy

  • Hazardous Substances Data Bank. CYCLOPHOSPHAMIDE .
  • Hazardous Substances Data Bank. DACTINOMYCIN .
  • Hazardous Substances Data Bank. VINCRISTINE .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16408493.001).
  • [ISSN] 0016-254X
  • [Journal-full-title] Fukuoka igaku zasshi = Hukuoka acta medica
  • [ISO-abbreviation] Fukuoka Igaku Zasshi
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 1CC1JFE158 / Dactinomycin; 5J49Q6B70F / Vincristine; 8N3DW7272P / Cyclophosphamide; VAC protocol
  •  go-up   go-down


9. Schrock A, Jakob M, Zhou H, Bootz F: Laryngeal pleomorphic rhabdomyosarcoma. Auris Nasus Larynx; 2007 Dec;34(4):553-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Laryngeal pleomorphic rhabdomyosarcoma.
  • Adult rhabdomyosarcoma of the larynx is a rare disease.
  • Two cases of laryngeal rhabdomyosarcoma of the pleomorphic subtype are presented.
  • [MeSH-major] Hoarseness / etiology. Laryngeal Neoplasms / diagnosis. Rhabdomyosarcoma / diagnosis

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17481838.001).
  • [ISSN] 0385-8146
  • [Journal-full-title] Auris, nasus, larynx
  • [ISO-abbreviation] Auris Nasus Larynx
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
  •  go-up   go-down


10. Meng MV, Grossfeld GD, Sudilovsky D, Baehner FL: Fine needle aspiration cytology of adult perineal rhabdomyosarcoma: a case report. Acta Cytol; 2006 Jan-Feb;50(1):88-92
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Fine needle aspiration cytology of adult perineal rhabdomyosarcoma: a case report.
  • BACKGROUND: Adult perineal soft tissue sarcomas are rare.
  • The diagnosis of rhabdomyosarcoma was favored on FNA and was corroborated by immunohistochemical stains for desmin, myogenin and CD56.
  • Upon surgical resection, the diagnosis of alveolar rhabdomyosarcoma was confirmed histologically and immunophenotypically.
  • CONCLUSION: FNA is a useful tool in diagnosing soft tissue lessions of the perineum, including rare primary tumors, such as adult rhabdomyosarcoma.
  • [MeSH-major] Perineum / pathology. Rhabdomyosarcoma / pathology. Soft Tissue Neoplasms / pathology
  • [MeSH-minor] Adult. Biomarkers, Tumor / metabolism. Biopsy, Fine-Needle. Desmin / metabolism. Humans. Male. Myogenin / metabolism

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16514847.001).
  • [ISSN] 0001-5547
  • [Journal-full-title] Acta cytologica
  • [ISO-abbreviation] Acta Cytol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Desmin; 0 / Myogenin
  •  go-up   go-down


11. El-Ghazali AM, McLaren KM: Embryonal rhabdomyosarcoma of adult nasopharynx. J Laryngol Otol; 2005 Aug;119(8):639-42
Genetic Alliance. consumer health - Rhabdomyosarcoma embryonal.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Embryonal rhabdomyosarcoma of adult nasopharynx.
  • Adult rhabdomyosarcomas in the head and neck are extremely rare and carry a poor prognosis.
  • The authors report a case of embryonal rhabdomyosarcoma in an adult nasopharynx treated with a combined modality treatment of chemotherapy and radiotherapy as per the European International Society of Paediatric Oncology (SIOP) MMT 89 study, group D.
  • [MeSH-major] Nasopharyngeal Neoplasms / therapy. Rhabdomyosarcoma, Embryonal / therapy

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16102222.001).
  • [ISSN] 0022-2151
  • [Journal-full-title] The Journal of laryngology and otology
  • [ISO-abbreviation] J Laryngol Otol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  •  go-up   go-down


12. Wakulińska A, Dembowska-Bagińska B, Cienciała M, Bothur-Nowacka J, Kościesza A, Pakuła-Kościesza I, Perek D: [Results of the treatment of paediatric non-rhabdomyosarcoma. One centre experience]. Med Wieku Rozwoj; 2006 Jul-Sep;10(3 Pt 1):819-29
MedlinePlus Health Information. consumer health - Soft Tissue Sarcoma.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Results of the treatment of paediatric non-rhabdomyosarcoma. One centre experience].
  • [Transliterated title] Wyniki leczenia miesaków tkanek miekkich nie-rhabdomyosarcoma w jednym ośrodku.
  • Non-rhabdomyosarcoma soft tissue sarcomas (NR STS) are a rare group of neoplasms of mesenchymal origin.
  • [MeSH-major] Sarcoma / epidemiology. Sarcoma / therapy. Soft Tissue Neoplasms / epidemiology. Soft Tissue Neoplasms / therapy
  • [MeSH-minor] Adolescent. Adult. Chemotherapy, Adjuvant. Child. Child, Preschool. Combined Modality Therapy. Female. Humans. Kaplan-Meier Estimate. Male. Poland / epidemiology. Radiotherapy, Adjuvant. Treatment Outcome

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17317913.001).
  • [Journal-full-title] Medycyna wieku rozwojowego
  • [ISO-abbreviation] Med Wieku Rozwoj
  • [Language] pol
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Poland
  •  go-up   go-down


13. Haga K, Kashiwagi A, Nagamori S, Yamashiro K: Adult paratesticular rhabdomyosarcoma. Nat Clin Pract Urol; 2005 Aug;2(8):398-402; quiz 403
MedlinePlus Health Information. consumer health - Testicular Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult paratesticular rhabdomyosarcoma.
  • DIAGNOSIS: Paratesticular rhabdomyosarcoma with lymph node metastasis.
  • [MeSH-major] Rhabdomyosarcoma. Testicular Neoplasms
  • [MeSH-minor] Adult. Humans. Male

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16474737.001).
  • [ISSN] 1743-4270
  • [Journal-full-title] Nature clinical practice. Urology
  • [ISO-abbreviation] Nat Clin Pract Urol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


14. Widemann BC, Fox E, Adamson PC, Baruchel S, Kim A, Ingle AM, Bender JG, Stempak D, Balis FM, Blaney SM: Phase I study of sorafenib in children with refractory solid tumors: A Children's Oncology Group Phase I Consortium trial. J Clin Oncol; 2009 May 20;27(15_suppl):10012

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • RESULTS: 34 eligible pts [16M, median age 14.6 yrs, (range, 5-21)] with osteosarcoma (n = 8), rhabdomyosarcoma (n = 3), other sarcomas (n = 13), hepatoblastoma (n = 3), or other solid tumors (n = 7) received 1-22 cycles (median 2).
  • CONCLUSIONS: The MTD of sorafenib in children with solid tumors is 200 mg/m<sup>2</sup>, similar to the adult recommended dose (400 mg).

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 27962524.001).
  • [ISSN] 1527-7755
  • [Journal-full-title] Journal of clinical oncology : official journal of the American Society of Clinical Oncology
  • [ISO-abbreviation] J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


15. Zalesska-Krecicka M, Jankowska-Konsur A, Krecicki T: [Rhabdomyosarcoma of nasopharynx and oropharynx in adult--a case report]. Otolaryngol Pol; 2005;59(5):759-62

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Rhabdomyosarcoma of nasopharynx and oropharynx in adult--a case report].
  • [Transliterated title] Przypadek rhabdomyosarcoma nosogardła i gardła środkowego u osoby dorosłej.
  • The authors present the case of rhabdomyosarcoma--a rare malignancy--in the adult patient.
  • [MeSH-major] Nasopharyngeal Neoplasms / diagnosis. Nasopharyngeal Neoplasms / surgery. Rhabdomyosarcoma / diagnosis. Rhabdomyosarcoma / therapy

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16471198.001).
  • [ISSN] 0030-6657
  • [Journal-full-title] Otolaryngologia polska = The Polish otolaryngology
  • [ISO-abbreviation] Otolaryngol Pol
  • [Language] pol
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Poland
  •  go-up   go-down


16. Shimamoto K, Tanji N, Ozaw A, Sasaki T, Ikeda T, Iseda T, Yokoyama M: [Intrascrotal rhabdomyosarcoma in adult: a case report]. Nihon Hinyokika Gakkai Zasshi; 2009 May;100(4):545-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Intrascrotal rhabdomyosarcoma in adult: a case report].
  • The pathological diagnosis of pleomorphic rhabdomyosarcoma arisen from the right spermatic cord was made.
  • Systemic chemotherapy with vincristine, actinomycin D, plus cyclophosphamide (VAC therapy), and etoposide plus cisplatin (EP therapy) were made according to Intergroup Rhabdomyosarcoma Study (IRS)-IV Regimen 45.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Chemotherapy, Adjuvant. Genital Neoplasms, Male / therapy. Lymph Node Excision. Orchiectomy. Radiotherapy, Adjuvant. Rhabdomyosarcoma / therapy. Scrotum

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19514277.001).
  • [ISSN] 0021-5287
  • [Journal-full-title] Nihon Hinyōkika Gakkai zasshi. The japanese journal of urology
  • [ISO-abbreviation] Nippon Hinyokika Gakkai Zasshi
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
  •  go-up   go-down


17. Croes R, Debiec-Rychter M, Cokelaere K, De Vos R, Hagemeijer A, Sciot R: Adult sclerosing rhabdomyosarcoma: cytogenetic link with embryonal rhabdomyosarcoma. Virchows Arch; 2005 Jan;446(1):64-7
NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult sclerosing rhabdomyosarcoma: cytogenetic link with embryonal rhabdomyosarcoma.
  • Rhabdomyosarcomas are classified into three well-defined categories: embryonal, alveolar and pleomorphic rhabdomyosarcoma.
  • Recently, seven cases of an unusual adult type of rhabdomyosarcoma with a prominent hyaline sclerosis have been described.
  • We report the hitherto unreported cytogenetic changes of an adult sclerosing rhabdomyosarcoma.
  • Using fluorescent in situ hybridization (FISH) analysis, the tumor cells were negative for FOXO1A-disrupting translocations specific for alveolar rhabdomyosarcoma.
  • The chromosomal composition of malignant cells resembled the pattern of numerical changes frequently observed in embryonal rhabdomyosarcoma, suggesting a close relationship of an adult sclerosing rhabdomyosarcoma with this entity.
  • [MeSH-major] Rhabdomyosarcoma / genetics. Rhabdomyosarcoma, Embryonal / genetics. Translocation, Genetic

  • Genetic Alliance. consumer health - Rhabdomyosarcoma embryonal.
  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15660283.001).
  • [ISSN] 0945-6317
  • [Journal-full-title] Virchows Archiv : an international journal of pathology
  • [ISO-abbreviation] Virchows Arch.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


18. Semino A, Danova M, Perlini S, Palladini G, Riccardi A, Perfetti V: Unusual manifestations of disseminated neoplasia at presentation: right-sided heart failure due to a massive cardiac metastasis and autoimmune thrombocytopenia in pleomorphic rhabdomyosarcoma of the adult. Am J Clin Oncol; 2006 Feb;29(1):102-3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Unusual manifestations of disseminated neoplasia at presentation: right-sided heart failure due to a massive cardiac metastasis and autoimmune thrombocytopenia in pleomorphic rhabdomyosarcoma of the adult.
  • This report describes the occurrence of a massive cardiac metastasis at diagnosis of leg rhabdomyosarcoma in a middle-age adult.
  • [MeSH-major] Heart Neoplasms / secondary. Rhabdomyosarcoma / secondary. Soft Tissue Neoplasms / pathology
  • [MeSH-minor] Adult. Comorbidity. Fatal Outcome. Heart Failure / etiology. Humans. Leg / pathology. Male. Purpura, Thrombocytopenic, Idiopathic / drug therapy

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16462513.001).
  • [ISSN] 1537-453X
  • [Journal-full-title] American journal of clinical oncology
  • [ISO-abbreviation] Am. J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


19. Ferrari A, Casanova M: Current chemotherapeutic strategies for rhabdomyosarcoma. Expert Rev Anticancer Ther; 2005 Apr;5(2):283-94

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Current chemotherapeutic strategies for rhabdomyosarcoma.
  • Rhabdomyosarcoma is a typical tumor of childhood and adolescence.
  • Rhabdomyosarcoma is a highly chemosensitive neoplasm, and the role of this therapeutic approach has also been clearly demonstrated in the adjuvant setting.
  • This review covers current concepts on chemotherapy for rhabdomyosarcoma, with an overview of the results of the main clinical trials conducted over recent years and considerations of possible strategies for the near future.
  • Recommendations for adult patients with rhabdomyosarcoma are also discussed, suggesting that these patients should be treated according to pediatric guidelines.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Rhabdomyosarcoma / drug therapy

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15877525.001).
  • [ISSN] 1744-8328
  • [Journal-full-title] Expert review of anticancer therapy
  • [ISO-abbreviation] Expert Rev Anticancer Ther
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 86
  •  go-up   go-down


20. Hulse N, Raja S, Kumar A, Paul AS: Rhabdomyosarcoma of the extremities in adults. Acta Orthop Belg; 2006 Apr;72(2):199-203

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rhabdomyosarcoma of the extremities in adults.
  • Extremity rhabdomyosarcoma is a highly malignant tumour and our results are poor compared to the reported results in children.
  • Metastatic recurrence is high in adult rhabdomyosarcomas even with local control of the disease and therefore development of effective systemic therapy is an urgent priority.
  • [MeSH-major] Extremities. Rhabdomyosarcoma / therapy. Soft Tissue Neoplasms / therapy
  • [MeSH-minor] Adult. Aged. Combined Modality Therapy. Female. Humans. Male. Middle Aged. Retrospective Studies

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16768266.001).
  • [ISSN] 0001-6462
  • [Journal-full-title] Acta orthopaedica Belgica
  • [ISO-abbreviation] Acta Orthop Belg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Belgium
  •  go-up   go-down


21. Zambrano E, Pérez-Atayde AR, Ahrens W, Reyes-Múgica M: Pediatric sclerosing rhabdomyosarcoma. Int J Surg Pathol; 2006 Jul;14(3):193-9
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Pediatric sclerosing rhabdomyosarcoma.
  • Sclerosing rhabdomyosarcoma, a particular phenotypic variant of rhabdomyosarcoma initially described in the adult population, has emerged as a potential pitfall in the evaluation of pediatric sarcomas.
  • Because of its densely hyalinized collagenous matrix and its occasional expression of a pseudovascular pattern of growth, sclerosing rhabdomyosarcoma has been at times misdiagnosed as chondrosarcoma, osteosarcoma, or angiosarcoma.
  • We describe 3 pediatric patients with sclerosing rhabdomyosarcoma and provide a detailed description of its distinguishing pathologic features.
  • Awareness about this rhabdomyosarcoma variant and careful immunophenotypical evaluation are necessary to establish the correct diagnosis.
  • Although no specific genetic aberrations have been recognized, yet the cytogenetic findings in 2 tumors of this series suggest a link with embryonal rhabdomyosarcoma.
  • It is likely that further genotyping will result in better nosologic delineation of sclerosing rhabdomyosarcoma and that it will uncover pathogenetically and prognostically relevant genes.
  • [MeSH-major] Rhabdomyosarcoma / pathology. Soft Tissue Neoplasms / pathology

  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16959698.001).
  • [ISSN] 1066-8969
  • [Journal-full-title] International journal of surgical pathology
  • [ISO-abbreviation] Int. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
  •  go-up   go-down


22. Lavaju P, Das H, Malla P, Tiwari A, Sinha A, Upadhyaya P: Orbital rhabdomyosarcoma in an adult. Nepal J Ophthalmol; 2010 Jan-Jun;2(1):64-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Orbital rhabdomyosarcoma in an adult.
  • INTRODUCTION: Rhabdomyosarcoma is the most common primary orbital malignant tumor in children.
  • Orbital lesions represent about 10 % of all the cases of rhabdomyosarcoma.
  • Rhabdomyosarcoma is a rare cause of proptosis in adults.
  • OBJECTIVE: To report a case of primary orbital rhabdomyosarcoma in a 45-year-old female.
  • The main outcome measures are a rare cause ofproptosis in an adult, discussion on treatment options and prognosis ofrhabdomyosarcoma.
  • CONCLUSION: Rhabdomyosarcoma is a rare cause of proptosis in adults.
  • [MeSH-minor] Female. Follow-Up Studies. Humans. Middle Aged. Orbital Neoplasms / diagnosis. Orbital Neoplasms / surgery. Rhabdomyosarcoma, Alveolar / diagnosis. Rhabdomyosarcoma, Alveolar / surgery. Tomography, X-Ray Computed

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 21141330.001).
  • [ISSN] 2072-6805
  • [Journal-full-title] Nepalese journal of ophthalmology : a biannual peer-reviewed academic journal of the Nepal Ophthalmic Society : NEPJOPH
  • [ISO-abbreviation] Nepal J Ophthalmol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Nepal
  • [Chemical-registry-number] Rhabdomyosarcoma of the orbit
  •  go-up   go-down


23. Chi AC, Barnes JD, Budnick S, Agresta SV, Neville B: Rhabdomyosarcoma of the maxillary gingiva. J Periodontol; 2007 Sep;78(9):1839-45
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rhabdomyosarcoma of the maxillary gingiva.
  • BACKGROUND: Rhabdomyosarcoma is a malignant neoplasm of primitive mesenchyme exhibiting skeletal muscle differentiation.
  • Oral rhabdomyosarcoma is rare and accounts for only 0.04% of all head and neck malignancies.
  • A diagnosis of embryonal rhabdomyosarcoma was made.
  • CONCLUSIONS: Oral rhabdomyosarcoma can develop insidiously.
  • [MeSH-major] Gingival Neoplasms / pathology. Rhabdomyosarcoma / pathology
  • [MeSH-minor] Adult. Female. Humans. Maxilla

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17760557.001).
  • [ISSN] 0022-3492
  • [Journal-full-title] Journal of periodontology
  • [ISO-abbreviation] J. Periodontol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 51
  •  go-up   go-down


24. Dausse F, Balu-Maestro C, Chapellier C, Leblanc-Talent P: Rhabdomyosarcoma of the breast. Clin Imaging; 2005 Sep-Oct;29(5):337-41
Hazardous Substances Data Bank. IFOSFAMIDE .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rhabdomyosarcoma of the breast.
  • AIM: The aim of this study was to describe the first imaging studies of a primary embryonal rhabdomyosarcoma of the breast in an adult woman.
  • CONCLUSION: Rhabdomyosarcoma is a rare tumor in adults; to our knowledge, this is the first report describing the imaging features and value of MRI for the work-up and follow-up of mammary rhabdomyosarcoma.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Breast Neoplasms / diagnosis. Breast Neoplasms / drug therapy. Rhabdomyosarcoma / diagnosis

  • MedlinePlus Health Information. consumer health - Breast Cancer.
  • Hazardous Substances Data Bank. DOXORUBICIN .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16153540.001).
  • [ISSN] 0899-7071
  • [Journal-full-title] Clinical imaging
  • [ISO-abbreviation] Clin Imaging
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antibiotics, Antineoplastic; 0 / Antineoplastic Agents, Alkylating; 80168379AG / Doxorubicin; UM20QQM95Y / Ifosfamide
  •  go-up   go-down


25. Childs L, Hull D, Bostwick DG: Adult urinary bladder rhabdomyosarcoma. Urology; 2008 Oct;72(4):948.e1-3
MedlinePlus Health Information. consumer health - Bladder Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult urinary bladder rhabdomyosarcoma.
  • We report a case of embryonal rhabdomyosarcoma arising in the bladder of a 39-year-old woman who presented with urgency, frequency, and gross hematuria.
  • [MeSH-major] Rhabdomyosarcoma / diagnosis. Urinary Bladder Neoplasms / diagnosis
  • [MeSH-minor] Adult. Female. Humans

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18400279.001).
  • [ISSN] 1527-9995
  • [Journal-full-title] Urology
  • [ISO-abbreviation] Urology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


26. Zhong J, Li ST, Yao XH, Jin B, Wan L: An intrasellar rhabdomyosarcoma misdiagnosed as pituitary adenoma. Surg Neurol; 2007;68 Suppl 2:S29-33; discussion S33
MedlinePlus Health Information. consumer health - Pituitary Tumors.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] An intrasellar rhabdomyosarcoma misdiagnosed as pituitary adenoma.
  • BACKGROUND: Rhabdomyosarcoma is a malignant tumor of the skeletal muscle cells.
  • No previous case of primary intrasellar rhabdomyosarcoma except for 1 case has been reported in the literature.
  • The patient was preoperatively diagnosed as pituitary adenoma, which was confirmed pathologically as rhabdomyosarcoma after the operation.
  • CONCLUSIONS: Our findings suggest that rhabdomyosarcoma should be considered in the differential diagnosis of a primary intrasellar neoplasm.
  • [MeSH-major] Adenoma / diagnosis. Diagnostic Errors. Pituitary Neoplasms / diagnosis. Rhabdomyosarcoma / diagnosis. Sella Turcica. Skull Neoplasms / diagnosis
  • [MeSH-minor] Adult. Fatal Outcome. Female. Humans

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18037040.001).
  • [ISSN] 0090-3019
  • [Journal-full-title] Surgical neurology
  • [ISO-abbreviation] Surg Neurol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


27. Lamovec J, Volavsek M: Sclerosing rhabdomyosarcoma of the parotid gland in an adult. Ann Diagn Pathol; 2009 Oct;13(5):334-8
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Sclerosing rhabdomyosarcoma of the parotid gland in an adult.
  • Primary rhabdomyosarcoma of salivary glands is an extremely rare neoplasm, mostly seen in children.
  • A newly described subtype of rhabdomyosarcoma, sclerosing rhabdomyosarcoma, has not yet been reported in this location.
  • Sclerosing rhabdomyosarcoma may cause differential diagnostic problems because it could be confounded for osteosarcoma, chondrosarcoma, and some other types of sarcoma, and as in our case, for myxofibrosarcoma and myoepithelial carcinoma.
  • Its location in the head and neck is of special interest because 6 of 14 previously described adult cases of sclerosing rhabdomyosarcoma and 7 of 18 pediatric cases also occurred in this region.
  • To our knowledge, this is the first reported case of primary sclerosing rhabdomyosarcoma of the parotid gland.
  • [MeSH-major] MyoD Protein / metabolism. Parotid Neoplasms / pathology. Rhabdomyosarcoma / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19751910.001).
  • [ISSN] 1532-8198
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / MyoD Protein; 0 / MyoD1 myogenic differentiation protein
  •  go-up   go-down


28. Dalfior D, Eccher A, Gobbo S, Brunelli M, Martignoni G, Menestrina F, Dalla PP, Dvornik G: Primary pleomorphic rhabdomyosarcoma of the kidney in an adult. Ann Diagn Pathol; 2008 Aug;12(4):301-3
MedlinePlus Health Information. consumer health - Kidney Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary pleomorphic rhabdomyosarcoma of the kidney in an adult.
  • Sarcoma of the kidney is uncommon and represents between 1% and 3% of all malignant renal tumors.
  • Primary rhabdomyosarcoma of the kidney in adult age is unusual, and only sporadic cases have been reported.
  • We report a new case of pleomorphic rhabdomyosarcoma of the kidney in an adult patient.
  • [MeSH-major] Kidney Neoplasms / pathology. Rhabdomyosarcoma / pathology
  • [MeSH-minor] Adult. Female. Humans. Immunohistochemistry

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18621001.001).
  • [ISSN] 1532-8198
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


29. Niimi K, Hashimoto Y, Kurokawa S, Okada A, Tozawa K, Kohri K: Embryonal rhabdomyosarcoma of the prostate. Int J Clin Oncol; 2010 Feb;15(1):93-6
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Embryonal rhabdomyosarcoma of the prostate.
  • We describe a case of embryonal rhabdomyosarcoma of the prostate in a 20-year-old man with a history of acute lymphatic leukemia at 6 years of age.
  • A biopsy of the prostate revealed embryonal rhabdomyosarcoma.
  • Chemotherapy with vincristine, actinomycin D, cyclophosphamide, and ifosfamide was begun according to the treatment protocol of the Japan Rhabdomyosarcoma Study Group.
  • It has been reported that 88% of postradiation sarcomas are KIT-positive, and we suspect that our patient suffered a postradiation sarcoma, because his tumor was KIT-positive.
  • This is the first report of postradiation sarcoma manifesting as an embryonal rhabdomyosarcoma of the prostate.
  • [MeSH-major] Neoplasms, Second Primary / drug therapy. Neoplasms, Second Primary / pathology. Precursor Cell Lymphoblastic Leukemia-Lymphoma / radiotherapy. Prostatic Neoplasms / drug therapy. Prostatic Neoplasms / pathology. Rhabdomyosarcoma / drug therapy. Rhabdomyosarcoma / pathology
  • [MeSH-minor] Adult. Humans. Male. Neoplasms, Radiation-Induced

  • Genetic Alliance. consumer health - Rhabdomyosarcoma embryonal.
  • MedlinePlus Health Information. consumer health - Prostate Cancer.
  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20087615.001).
  • [ISSN] 1437-7772
  • [Journal-full-title] International journal of clinical oncology
  • [ISO-abbreviation] Int. J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
  •  go-up   go-down


30. Adigun IA, Rahman GA, Buhari MO, Ogundipe KO, Omotayo JA: Pattern of rhabdomyosarcoma in Nigerian children. J Natl Med Assoc; 2008 Aug;100(8):906-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Pattern of rhabdomyosarcoma in Nigerian children.
  • This study was conducted to show the prevalence and pattern of distribution of rhabdomyosarcoma among children in a black African population.
  • The records of patients with rhabdomyosarcoma were analyzed in details.
  • Rhabdomyosarcoma constitutes 9.5% of the total number of patients managed, and 54.5% of these patients are age < 20 years.
  • [MeSH-major] Rhabdomyosarcoma / epidemiology
  • [MeSH-minor] Adolescent. Adult. African Continental Ancestry Group / statistics & numerical data. Age Distribution. Aged. Child. Child, Preschool. Developing Countries / statistics & numerical data. Hospitals, Teaching / statistics & numerical data. Humans. Infant. Infant, Newborn. Middle Aged. Nigeria / epidemiology. Prevalence. Retrospective Studies

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18717141.001).
  • [ISSN] 1943-4693
  • [Journal-full-title] Journal of the National Medical Association
  • [ISO-abbreviation] J Natl Med Assoc
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


31. Choi JS, Choi JS, Kim EJ: Primary pulmonary rhabdomyosarcoma in an adult with neurofibromatosis-1. Ann Thorac Surg; 2009 Oct;88(4):1356-8
MedlinePlus Health Information. consumer health - Lung Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary pulmonary rhabdomyosarcoma in an adult with neurofibromatosis-1.
  • We report a unique case of primary pulmonary rhabdomyosarcoma in an adult with neurofibromatosis type 1.
  • The Intergroup Rhabdomyosarcoma Study IV postsurgical grouping classification was 1A.
  • [MeSH-major] Lung Neoplasms / etiology. Neurofibromatosis 1 / complications. Rhabdomyosarcoma / etiology
  • [MeSH-minor] Adult. Biopsy, Needle. Diagnosis, Differential. Humans. Male. Pneumonectomy / methods. Tomography, X-Ray Computed

  • Genetic Alliance. consumer health - Neurofibromatosis.
  • Genetic Alliance. consumer health - Rhabdomyosarcoma 1.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19766846.001).
  • [ISSN] 1552-6259
  • [Journal-full-title] The Annals of thoracic surgery
  • [ISO-abbreviation] Ann. Thorac. Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
  •  go-up   go-down


32. Fountas KN, Donner RS, Nikolakakos LG, Feltes CH, Karampelas I, Robinson JS Jr: Adult paravertebral pleomorphic rhabdomyosarcoma infiltrating diffusely the whole spinal axis. Case report. J Neurosurg Spine; 2005 Mar;2(3):344-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult paravertebral pleomorphic rhabdomyosarcoma infiltrating diffusely the whole spinal axis. Case report.
  • The authors report a unique case of diffuse spinal metastatic disease due to a pleomorphic rhabdomyosarcoma (RMS) in an adult.
  • [MeSH-major] Rhabdomyosarcoma / pathology. Spinal Neoplasms / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15796361.001).
  • [ISSN] 1547-5654
  • [Journal-full-title] Journal of neurosurgery. Spine
  • [ISO-abbreviation] J Neurosurg Spine
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


33. Kratz CP, Holter S, Etzler J, Lauten M, Pollett A, Niemeyer CM, Gallinger S, Wimmer K: Rhabdomyosarcoma in patients with constitutional mismatch-repair-deficiency syndrome. J Med Genet; 2009 Jun;46(6):418-20
SciCrunch. OMIM: Data: Gene Annotation .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rhabdomyosarcoma in patients with constitutional mismatch-repair-deficiency syndrome.
  • RESULTS: We analysed two consanguineous families that had members with suspected CMMR-D syndrome who developed rhabdomyosarcoma among other neoplasias.
  • In family 2, immunohistochemistry analysis showed isolated loss of PMS2 expression in all tumours in the affected patients, including rhabdomyosarcoma itself and the surrounding normal tissue.
  • CONCLUSION: Together, these two new cases show that rhabdomyosarcoma and possibly other embryonic tumours, such as neuroblastoma and Wilm tumour, belong to the tumour spectrum of CMMR-D syndrome.
  • [MeSH-major] DNA Mismatch Repair / genetics. DNA Repair-Deficiency Disorders / genetics. Rhabdomyosarcoma / genetics
  • [MeSH-minor] Adaptor Proteins, Signal Transducing / genetics. Adaptor Proteins, Signal Transducing / metabolism. Adenosine Triphosphatases / genetics. Adenosine Triphosphatases / metabolism. Child. DNA Repair Enzymes / genetics. DNA Repair Enzymes / metabolism. DNA-Binding Proteins / genetics. DNA-Binding Proteins / metabolism. Female. Humans. Immunohistochemistry. Male. MutS Homolog 2 Protein / genetics. MutS Homolog 2 Protein / metabolism. Mutation. Neoplasms / genetics. Neoplasms / metabolism. Nuclear Proteins / genetics. Nuclear Proteins / metabolism. Pedigree. Sequence Analysis, DNA. Syndrome. Young Adult

  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19293170.001).
  • [ISSN] 1468-6244
  • [Journal-full-title] Journal of medical genetics
  • [ISO-abbreviation] J. Med. Genet.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Adaptor Proteins, Signal Transducing; 0 / DNA-Binding Proteins; 0 / G-T mismatch-binding protein; 0 / MLH1 protein, human; 0 / Nuclear Proteins; EC 3.6.1.- / Adenosine Triphosphatases; EC 3.6.1.- / PMS2 protein, human; EC 3.6.1.3 / MSH2 protein, human; EC 3.6.1.3 / MutS Homolog 2 Protein; EC 6.5.1.- / DNA Repair Enzymes
  •  go-up   go-down


34. Grebe HP, Steube D: Primary cerebral rhabdomyosarcoma presenting as haemorrhagic stroke. Zentralbl Neurochir; 2008 May;69(2):93-5
MedlinePlus Health Information. consumer health - Stroke.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary cerebral rhabdomyosarcoma presenting as haemorrhagic stroke.
  • Histological analysis proved it to be an embryonal rhabdomyosarcoma.
  • We present this case as a rare aetiology of intracerebral haemorrhage, more frequently associated with arterial hypertension or vascular pathology, as well as being an unusual manifestation of embryonal rhabdomyosarcoma, rarely found in the brain.
  • [MeSH-major] Brain Neoplasms / diagnosis. Cerebral Hemorrhage / diagnosis. Rhabdomyosarcoma / diagnosis. Stroke / diagnosis
  • [MeSH-minor] Adult. Aphasia / etiology. Brain / pathology. Brain / radiography. Brain / radionuclide imaging. Combined Modality Therapy. Female. Headache / etiology. Humans. Immunohistochemistry. Neoplasm Recurrence, Local. Neurosurgical Procedures. Palliative Care. Paresis / etiology. Tomography, X-Ray Computed

  • MedlinePlus Health Information. consumer health - Brain Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18444223.001).
  • [ISSN] 0044-4251
  • [Journal-full-title] Zentralblatt für Neurochirurgie
  • [ISO-abbreviation] Zentralbl. Neurochir.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


35. Houghton JP, McCluggage WG: Embryonal rhabdomyosarcoma of the cervix with focal pleomorphic areas. J Clin Pathol; 2007 Jan;60(1):88-9
International Agency for Research on Cancer - Screening Group. diagnostics - Histopathology and cytopathology of the uterine cervix - digital atlas .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Embryonal rhabdomyosarcoma of the cervix with focal pleomorphic areas.
  • An embryonal rhabdomyosarcoma (sarcoma botryoides) of the cervix occurring in a 30-year-old woman is described.
  • In addition to typical areas of the embryonal rhabdomyosarcoma, including cartilaginous elements, the neoplasm was characterised by the presence of foci composed of highly pleomorphic cells.
  • These foci may represent areas of dedifferentiation in an embryonal rhabdomyosarcoma.
  • [MeSH-major] Rhabdomyosarcoma, Embryonal / pathology. Uterine Cervical Neoplasms / pathology
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Humans. Polyps / pathology

  • Genetic Alliance. consumer health - Rhabdomyosarcoma embryonal.
  • MedlinePlus Health Information. consumer health - Cervical Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Int J Gynecol Cancer. 2002 Jan-Feb;12(1):128-32 [11860548.001]
  • [Cites] Int J Gynecol Pathol. 2004 Jan;23(1):78-82 [14668557.001]
  • [Cites] Obstet Gynecol. 1968 May;31(5):689-94 [5651112.001]
  • [Cites] Mt Sinai J Med. 1971 Jul-Aug;38(4):363-74 [5314782.001]
  • [Cites] Arch Gynecol Obstet. 2004 Dec;270(4):278-80 [12942264.001]
  • [Cites] Gynecol Oncol. 1988 Mar;29(3):290-304 [3278956.001]
  • [Cites] Hum Pathol. 1990 Apr;21(4):363-81 [2156771.001]
  • [Cites] Am J Surg Pathol. 1993 May;17(5):443-53 [8470759.001]
  • [Cites] J Reprod Med. 1999 Mar;44(3):306-8 [10202753.001]
  • [Cites] Cancer. 1987 Oct 1;60(7):1552-60 [3621128.001]
  • (PMID = 17213352.001).
  • [ISSN] 0021-9746
  • [Journal-full-title] Journal of clinical pathology
  • [ISO-abbreviation] J. Clin. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC1860605
  •  go-up   go-down


36. Nakagawa N, Tsuda T, Yamamoto M, Ito T, Futani H, Yamanishi K: Adult cutaneous alveolar rhabdomyosarcoma on the face diagnosed by the expression of PAX3-FKHR gene fusion transcripts. J Dermatol; 2008 Jul;35(7):462-7
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult cutaneous alveolar rhabdomyosarcoma on the face diagnosed by the expression of PAX3-FKHR gene fusion transcripts.
  • The histology was compatible with alveolar rhabdomyosarcoma, but immunohistochemistry showed that the tumor cells were negative for desmin, alpha-smooth muscle actin and alpha-Sr-1, but were positive for CD56, vimentin and myogenin.
  • The diagnosis of alveolar rhabdomyosarcoma was confirmed by the detection of PAX3-FKHR fusion gene transcripts in the paraffin-embedded tumor tissue.
  • This adult case of an alveolar rhabdomyosarcoma primarily occurring on the face is very rare, and the detection of PAX3-FKHR fusion gene transcripts was useful for diagnosis of the disease.
  • [MeSH-major] Facial Neoplasms / diagnosis. Oncogene Proteins, Fusion / metabolism. Rhabdomyosarcoma, Alveolar / diagnosis. Skin Neoplasms / diagnosis
  • [MeSH-minor] Adult. Female. Humans. RNA, Messenger / metabolism

  • Genetic Alliance. consumer health - Rhabdomyosarcoma alveolar.
  • MedlinePlus Health Information. consumer health - Skin Cancer.
  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18705836.001).
  • [ISSN] 0385-2407
  • [Journal-full-title] The Journal of dermatology
  • [ISO-abbreviation] J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Japan
  • [Chemical-registry-number] 0 / Oncogene Proteins, Fusion; 0 / PAX3-FKHR fusion protein, human; 0 / RNA, Messenger
  •  go-up   go-down


37. Shayah A, Agada FO, Karsai L, Stafford N: Adult laryngeal rhabdomyosarcoma: report of a case and literature review. Ann Afr Med; 2007 Dec;6(4):190-3

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult laryngeal rhabdomyosarcoma: report of a case and literature review.
  • Rhabdomyosarcoma is relatively seen in the pediatric age group with the head and neck region as the commonest site.
  • To the best of our knowledge, few cases of laryngeal involvement in adult have been described in the literature.
  • Biologically, rhabdomyosarcoma is different from squamous cell carcinoma, which is the commonest tumor of the larynx.
  • Histology confirmed a completely excised laryngeal rhabdomyosarcoma.
  • Rhabdomyosarcoma of larynx in adult is a rare disease.
  • [MeSH-major] Laryngeal Neoplasms / diagnosis. Rhabdomyosarcoma / diagnosis

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18354945.001).
  • [ISSN] 1596-3519
  • [Journal-full-title] Annals of African medicine
  • [ISO-abbreviation] Ann Afr Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Nigeria
  • [Number-of-references] 17
  •  go-up   go-down


38. Hatton MP, Green L, Boulos PR, Rubin PA: Rhabdomyosarcoma metastases to all extraocular muscles. Ophthal Plast Reconstr Surg; 2008 Jul-Aug;24(4):336-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rhabdomyosarcoma metastases to all extraocular muscles.
  • She had a history of rhabdomyosarcoma of the left orbit treated 2 years previously with chemotherapy and radiation.
  • Extraocular muscle biopsy confirmed rhabdomyosarcoma.
  • [MeSH-major] Muscle Neoplasms / secondary. Oculomotor Muscles / pathology. Orbital Neoplasms / pathology. Rhabdomyosarcoma / secondary
  • [MeSH-minor] Adult. Biomarkers, Tumor / analysis. Exophthalmos / etiology. Fatal Outcome. Female. Humans. Hypertrophy. Magnetic Resonance Imaging. Neoplasm Proteins / analysis. Tomography, X-Ray Computed

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18645454.001).
  • [ISSN] 0740-9303
  • [Journal-full-title] Ophthalmic plastic and reconstructive surgery
  • [ISO-abbreviation] Ophthal Plast Reconstr Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Neoplasm Proteins
  •  go-up   go-down


39. Ahmed AA, Tsokos M: Sinonasal rhabdomyosarcoma in children and young adults. Int J Surg Pathol; 2007 Apr;15(2):160-5
NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Sinonasal rhabdomyosarcoma in children and young adults.
  • Rhabdomyosarcoma is an aggressive malignant tumor often developing in the head and neck in children.
  • In the sinonasal region, rhabdomyosarcoma constitutes a clinically important group because of the difficulty of surgical resection and its generally poor prognosis.
  • We reviewed the archival pathology materials of 39 cases of rhabdomyosarcoma of the head and neck in children and young adults.
  • Only one case was classified as embryonal rhabdomyosarcoma.
  • Four alveolar rhabdomyosarcoma tumors were tested by RT-PCR; all showed PAX3/FKHR chromosomal translocation.
  • We conclude that sinonasal rhabdomyosarcoma is predominantly of the alveolar subtype and frequently shows clear cells.
  • [MeSH-major] Paranasal Sinus Neoplasms / pathology. Rhabdomyosarcoma, Alveolar / pathology. Rhabdomyosarcoma, Embryonal / pathology
  • [MeSH-minor] Adolescent. Adult. Biomarkers, Tumor / metabolism. Child. Desmin / metabolism. Female. Forkhead Transcription Factors / genetics. Forkhead Transcription Factors / metabolism. Humans. Male. Myogenin / metabolism. Paired Box Transcription Factors / genetics. Paired Box Transcription Factors / metabolism. Recombinant Fusion Proteins / genetics. Recombinant Fusion Proteins / metabolism. Translocation, Genetic

  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17478770.001).
  • [ISSN] 1066-8969
  • [Journal-full-title] International journal of surgical pathology
  • [ISO-abbreviation] Int. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Desmin; 0 / FOXO1 protein, human; 0 / Forkhead Transcription Factors; 0 / Myogenin; 0 / PAX3 protein, human; 0 / Paired Box Transcription Factors; 0 / Recombinant Fusion Proteins
  •  go-up   go-down


40. Kalu E, Creighton SM, Woodhouse CR: Vaginal restoration in survivors of childhood rhabdomyosarcoma. Int J Gynecol Cancer; 2009 Jul;19(5):981-4
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Vaginal restoration in survivors of childhood rhabdomyosarcoma.
  • Childhood genital rhabdomyosarcoma is a devastating diagnosis.
  • This management is, however, increasingly successful, and survival into adolescent and adult life is becoming more commonplace.
  • [MeSH-major] Reconstructive Surgical Procedures / methods. Rhabdomyosarcoma / surgery. Vagina / surgery. Vaginal Neoplasms / surgery
  • [MeSH-minor] Adolescent. Adult. Female. Humans. Survival Rate. Survivors. Young Adult

  • MedlinePlus Health Information. consumer health - Plastic and Cosmetic Surgery.
  • MedlinePlus Health Information. consumer health - Vaginal Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19574797.001).
  • [ISSN] 1525-1438
  • [Journal-full-title] International journal of gynecological cancer : official journal of the International Gynecological Cancer Society
  • [ISO-abbreviation] Int. J. Gynecol. Cancer
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


41. Goosens V, Van den Berghe I, De Clercq C, Casselman J: Radiation-induced mandibular adult spindle cell rhabdomyosarcoma. Int J Oral Maxillofac Surg; 2008 Apr;37(4):395-7
MedlinePlus Health Information. consumer health - Radiation Therapy.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Radiation-induced mandibular adult spindle cell rhabdomyosarcoma.
  • Spindle cell rhabdomyosarcoma (RMS), a variant of embryonal RMS, is a rare tumour, especially in adults.
  • [MeSH-major] Mandibular Neoplasms / etiology. Neoplasms, Radiation-Induced / etiology. Neoplasms, Second Primary / etiology. Radiotherapy / adverse effects. Rhabdomyosarcoma, Embryonal / etiology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18023143.001).
  • [ISSN] 0901-5027
  • [Journal-full-title] International journal of oral and maxillofacial surgery
  • [ISO-abbreviation] Int J Oral Maxillofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
  •  go-up   go-down


42. Cil T, Altintas A, Isikdogan A: Rhabdomyosarcoma presenting with destructive large lesion of the face. South Med J; 2008 Jan;101(1):104-5
MedlinePlus Health Information. consumer health - Soft Tissue Sarcoma.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rhabdomyosarcoma presenting with destructive large lesion of the face.
  • Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children and adolescents.
  • She was diagnosed with alveolar rhabdomyosarcoma on histopathological examination.
  • [MeSH-major] Facial Neoplasms / diagnosis. Rhabdomyosarcoma, Alveolar / diagnosis. Sarcoma / diagnosis
  • [MeSH-minor] Adult. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Combined Modality Therapy. Female. Humans. Immunohistochemistry

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18176304.001).
  • [ISSN] 1541-8243
  • [Journal-full-title] Southern medical journal
  • [ISO-abbreviation] South. Med. J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


43. Silvestris N, Zito FA, Resta L, Popescu O, Rossi R, Montemurro S, Colucci G: Unique case of giant adult paratesticular spindle cell rhabdomyosarcoma. Urology; 2009 Mar;73(3):500-2

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Unique case of giant adult paratesticular spindle cell rhabdomyosarcoma.
  • The final pathological diagnosis was paratesticular spindle cell rhabdomyosarcoma.
  • [MeSH-major] Genital Neoplasms, Male / pathology. Rhabdomyosarcoma / pathology. Scrotum

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19036416.001).
  • [ISSN] 1527-9995
  • [Journal-full-title] Urology
  • [ISO-abbreviation] Urology
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


44. Kordek R, Sowa P, Panasiuk M, Kmieciak M, Chudobinski C, Pluciennik E, Bednarek AK, Potemski P, Jesionek-Kupnicka D: Primary osseous rhabdomyosarcoma with focal matrix formation mimicking osteosarcoma. Pathol Res Pract; 2007;203(12):873-7
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary osseous rhabdomyosarcoma with focal matrix formation mimicking osteosarcoma.
  • We present an unusual case of primary osseous pleomorphic rhabdomyosarcoma with focal matrix formation mimicking osteosarcoma.
  • Desmin, actin, Myf4, and MyoD1 were positive in tumor cells, and a diagnosis of rhabdomyosarcoma was eventually made.
  • Only few cases of primary pure bone rhabdomyosarcoma have been reported.
  • Our case does not meet the criteria for sclerosing rhabdomyosarcoma, as matrix formation is focal and cells are spindle-shaped and pleomorphic.
  • [MeSH-major] Bone Neoplasms / diagnosis. Osteosarcoma / diagnosis. Rhabdomyosarcoma / diagnosis
  • [MeSH-minor] Actins / analysis. Adult. Biomarkers, Tumor / analysis. Desmin / analysis. Diagnosis, Differential. Humans. Magnetic Resonance Imaging. Male. MyoD Protein / analysis. Myogenin / analysis

  • Genetic Alliance. consumer health - Osteosarcoma.
  • MedlinePlus Health Information. consumer health - Bone Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17905523.001).
  • [ISSN] 0344-0338
  • [Journal-full-title] Pathology, research and practice
  • [ISO-abbreviation] Pathol. Res. Pract.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Actins; 0 / Biomarkers, Tumor; 0 / Desmin; 0 / MYOG protein, human; 0 / MyoD Protein; 0 / MyoD1 myogenic differentiation protein; 0 / Myogenin
  •  go-up   go-down


45. Li QX, Liu CX, Chun CP, Qi Y, Chang B, Nong WX, Yao ES, Li HA, Li F: [Comparative genomic hybridization: the profile of chromosomal imbalances in rhabdomyosarcoma]. Zhonghua Bing Li Xue Za Zhi; 2008 Aug;37(8):536-41
NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Comparative genomic hybridization: the profile of chromosomal imbalances in rhabdomyosarcoma].
  • OBJECTIVE: To characterize the profile of chromosomal imbalances of rhabdomyosarcoma(RMS).
  • METHODS: Comparative genomic hybridization (CGH) was used to investigate genomic imbalances in 25 cases of primary RMS including 10 cases of alveolar rhabdomyosarcoma (ARM), 12 cases of embryonic rhabdomyosarcoma (ERMS), 3 cases of polymorphic rhabdomyosarcoma (PRMS) and 2 RMS cell lines (A240 originated from ARMS and RD from PRMS), with correlation to histological type, pathologic grading, clinical staging, gender and age, respectively.
  • [MeSH-major] Carcinoma, Squamous Cell / genetics. Chromosome Aberrations. Chromosome Deletion. Comparative Genomic Hybridization / methods. Gene Fusion. Rhabdomyosarcoma / genetics
  • [MeSH-minor] Adolescent. Adult. Aged. Child. Child, Preschool. Chromosomes. Female. Humans. Infant. Male. Middle Aged. Neoplasm Staging. Spectral Karyotyping / methods. Young Adult

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19094465.001).
  • [ISSN] 0529-5807
  • [Journal-full-title] Zhonghua bing li xue za zhi = Chinese journal of pathology
  • [ISO-abbreviation] Zhonghua Bing Li Xue Za Zhi
  • [Language] chi
  • [Publication-type] Comparative Study; English Abstract; Journal Article
  • [Publication-country] China
  •  go-up   go-down


46. Ferguson SE, Gerald W, Barakat RR, Chi DS, Soslow RA: Clinicopathologic features of rhabdomyosarcoma of gynecologic origin in adults. Am J Surg Pathol; 2007 Mar;31(3):382-9
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Clinicopathologic features of rhabdomyosarcoma of gynecologic origin in adults.
  • Rhabdomyosarcoma (RMS) is the most common soft tissue tumor found in children.
  • The purpose of this study was to describe the clinical and pathologic features of RMS of the adult female genital tract.
  • Adult RMS of gynecologic origin presents with locoregional disease and most are morphologically similar to pediatric RMS; however, adult RMS behaves more aggressively, with worse overall survival.
  • [MeSH-major] Genital Neoplasms, Female / pathology. Rhabdomyosarcoma / pathology
  • [MeSH-minor] Adolescent. Adult. Aged. Combined Modality Therapy. Disease-Free Survival. Female. Gynecologic Surgical Procedures. Humans. Middle Aged. Neoplasm Recurrence, Local. Neoplasm Staging. Retrospective Studies

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [CommentIn] Am J Surg Pathol. 2008 Jan;32(1):174 [18162788.001]
  • (PMID = 17325479.001).
  • [ISSN] 0147-5185
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


47. Ustuner Z, Basaran M, Dizdar Y, Agaoglu FY, Bilgic B, Sakar B, Basaran GA, Darendeliler E, Ozger H, Onat H, Bavbek S: Clinical outcome of rhabdomyosarcoma in adolescent and adult patients: single center experience from Turkey. Tohoku J Exp Med; 2007 Nov;213(3):221-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Clinical outcome of rhabdomyosarcoma in adolescent and adult patients: single center experience from Turkey.
  • Rhabdomyosarcoma (RMS) is rare disease in adults (age >or= 16 years).
  • In this study, we report a single institution's experience in the treatment of adult RMS.
  • The tumor size, serum LDH level, and metastatic disease at the time of diagnosis are potential predictors of outcome in patients with adult RMS.
  • Adult RMS is an aggressive disease with poor survival despite treatment.
  • The data from prospective, randomized multicenter trials are necessary in order to improve the clinical outcome of adult RMS patients.
  • [MeSH-major] Rhabdomyosarcoma / mortality. Rhabdomyosarcoma / therapy
  • [MeSH-minor] Adolescent. Adult. Age Factors. Aged. Disease-Free Survival. Female. Humans. L-Lactate Dehydrogenase / metabolism. Male. Middle Aged. Retrospective Studies. Time Factors. Treatment Outcome. Turkey

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17984619.001).
  • [ISSN] 0040-8727
  • [Journal-full-title] The Tohoku journal of experimental medicine
  • [ISO-abbreviation] Tohoku J. Exp. Med.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] EC 1.1.1.27 / L-Lactate Dehydrogenase
  •  go-up   go-down


48. Nascimento AF, Fletcher CD: Spindle cell rhabdomyosarcoma in adults. Am J Surg Pathol; 2005 Aug;29(8):1106-13
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Spindle cell rhabdomyosarcoma in adults.
  • The spindle cell variant of rhabdomyosarcoma (RMS) is uncommon and is most often encountered in the paratesticular region of children in whom it has a good prognosis.
  • [MeSH-major] Rhabdomyosarcoma, Embryonal / pathology. Sarcoma / pathology
  • [MeSH-minor] Actins / analysis. Adolescent. Adult. Aged. Desmin / analysis. Female. Glial Fibrillary Acidic Protein / analysis. Humans. Immunohistochemistry. Keratins / analysis. Male. Middle Aged. Mucin-1. Myogenic Regulatory Factors / analysis. Myoglobin / analysis. Myosins / analysis. S100 Proteins / analysis

  • MedlinePlus Health Information. consumer health - Soft Tissue Sarcoma.
  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16006807.001).
  • [ISSN] 0147-5185
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Actins; 0 / Desmin; 0 / Glial Fibrillary Acidic Protein; 0 / Mucin-1; 0 / Myogenic Regulatory Factors; 0 / Myoglobin; 0 / S100 Proteins; 0 / myogenic factor 6; 68238-35-7 / Keratins; EC 3.6.4.1 / Myosins
  •  go-up   go-down


49. Leventhal DD, Spiegel J, Keane W: Laryngeal alveolar rhabdomyosarcoma involving the true vocal fold in an adult: Case report. Ear Nose Throat J; 2010 Dec;89(12):E8
Genetic Alliance. consumer health - Rhabdomyosarcoma alveolar.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Laryngeal alveolar rhabdomyosarcoma involving the true vocal fold in an adult: Case report.
  • Rhabdomyosarcoma of the larynx is extremely rare in adults, as only 17 well-documented cases have been previously reported in the English-language literature.
  • Of these, only 2 cases (both male) involved the alveolar subtype of rhabdomyosarcoma, and neither involved the true vocal folds.
  • We report a case of alveolar rhabdomyosarcoma of the true vocal fold in 54-year-old woman.
  • Management of head and neck rhabdomyosarcoma has evolved from radical surgery to less morbid procedures supplemented with radiation and chemotherapy.
  • However, because this tumor is so rare in the adult population, no adult-specific treatment regimen has emerged.
  • [MeSH-major] Laryngeal Neoplasms / pathology. Laryngeal Neoplasms / therapy. Rhabdomyosarcoma, Alveolar / pathology. Rhabdomyosarcoma, Alveolar / therapy. Vocal Cords / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 21174270.001).
  • [ISSN] 1942-7522
  • [Journal-full-title] Ear, nose, & throat journal
  • [ISO-abbreviation] Ear Nose Throat J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  •  go-up   go-down


50. Koukourakis GV, Kouloulias V, Zacharias G, Maravelis G, Papadimitriou C, Platoni K, Gouliamos A: Embryonal rhabdomyosarcoma of the uterine cervix. Clin Transl Oncol; 2009 Jun;11(6):399-402
Hazardous Substances Data Bank. IFOSFAMIDE .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Embryonal rhabdomyosarcoma of the uterine cervix.
  • INTRODUCTION: Embryonal rhabdomyosarcoma (RMS) of the uterine cervix is a rare and extremely malignant entity.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Hysterectomy. Radiotherapy, Adjuvant. Rhabdomyosarcoma, Embryonal / therapy. Uterine Cervical Neoplasms / therapy
  • [MeSH-minor] Brachytherapy. Chemotherapy, Adjuvant. Cisplatin / administration & dosage. Combined Modality Therapy. Diagnostic Errors. Etoposide / administration & dosage. Female. Humans. Ifosfamide / administration & dosage. Lymph Node Excision. Ovariectomy. Particle Accelerators. Photons / therapeutic use. Polyps / diagnosis. Polyps / pathology. Polyps / surgery. Radiotherapy, Conformal. Remission Induction. Uterine Hemorrhage / etiology. Young Adult


51. Becker V, Gaa J, Ott K, Seemann M, Becker K, Schmid R: A rare case of primary rectal rhabdomyosarcoma in an adult. Z Gastroenterol; 2006 Nov;44(11):1149-52

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A rare case of primary rectal rhabdomyosarcoma in an adult.
  • We report an extremely rare case (1:200 000) of primary rectal rhabdomyosarcoma (RMS) in an adult.
  • In the literature, this case report is the first one dealing with an adult patient.
  • [MeSH-major] Rectal Neoplasms / diagnosis. Rectal Neoplasms / therapy. Rhabdomyosarcoma / diagnosis. Rhabdomyosarcoma / therapy
  • [MeSH-minor] Adult. Diagnosis, Differential. Humans. Male

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17115357.001).
  • [ISSN] 0044-2771
  • [Journal-full-title] Zeitschrift für Gastroenterologie
  • [ISO-abbreviation] Z Gastroenterol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


52. Cantley RL, Cimbaluk D, Reddy V, Iacusso C, Gattuso P: Fine-needle aspiration diagnosis of a metastatic adult sclerosing rhabdomyosarcoma in a lymph node. Diagn Cytopathol; 2010 Oct;38(10):761-4

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Fine-needle aspiration diagnosis of a metastatic adult sclerosing rhabdomyosarcoma in a lymph node.
  • Adult sclerosing rhabdomyosarcoma (ASRMS) is a rare variant of rhabdomyosarcoma with a characteristic histological appearance of small, round cells in a dense, hyalinized stroma.
  • This case highlights the cytologic features of a rare form of rhabdomyosarcoma, and emphasizes the utility of FNA in the assessment of lymphadenopathy in the setting of a soft-tissue sarcoma.
  • [MeSH-major] Biopsy, Fine-Needle. Lymphatic Metastasis / pathology. Rhabdomyosarcoma / secondary. Soft Tissue Neoplasms / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Copyright] © 2010 Wiley-Liss, Inc.
  • (PMID = 20091893.001).
  • [ISSN] 1097-0339
  • [Journal-full-title] Diagnostic cytopathology
  • [ISO-abbreviation] Diagn. Cytopathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


53. Meir K, Wygoda M, Reichman O, Gofrit ON, Pizov G: Puerperal renal rhabdomyosarcoma: case report and review of the literature. Urol Oncol; 2006 Jan-Feb;24(1):40-3
MedlinePlus Health Information. consumer health - Tumors and Pregnancy.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Puerperal renal rhabdomyosarcoma: case report and review of the literature.
  • Renal rhabdomyosarcoma is a rare malignant mesenchymal tumor with an aggressive clinical course.
  • We describe the case of a 39-year-old woman with a large rhabdomyosarcoma of the left kidney serendipitously discovered ultrasonographically subsequent to cesarean section.
  • To our knowledge, this is the first reported case of renal rhabdomyosarcoma during pregnancy.
  • [MeSH-major] Kidney Neoplasms / pathology. Kidney Neoplasms / ultrasonography. Pregnancy Complications, Neoplastic / pathology. Pregnancy Complications, Neoplastic / ultrasonography. Rhabdomyosarcoma / pathology. Rhabdomyosarcoma / ultrasonography
  • [MeSH-minor] Adult. Cesarean Section. Female. Humans. Pregnancy. Puerperal Disorders

  • MedlinePlus Health Information. consumer health - Kidney Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16414492.001).
  • [ISSN] 1078-1439
  • [Journal-full-title] Urologic oncology
  • [ISO-abbreviation] Urol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


54. Kourda N, El Atat R, Derouiche A, Bettaib I, Baltagi S, Zermani R: [Paratesticular pleomorphic rhabdomyosarcoma in an adult: diagnosis and management]. Cancer Radiother; 2007 Sep;11(5):280-3
MedlinePlus Health Information. consumer health - Testicular Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Paratesticular pleomorphic rhabdomyosarcoma in an adult: diagnosis and management].
  • A paratesticular pleomorphic rhabdomyosarcoma occurring in a 63-year old man is reported.
  • [MeSH-major] Rhabdomyosarcoma. Testicular Neoplasms

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17611140.001).
  • [ISSN] 1278-3218
  • [Journal-full-title] Cancer radiothérapie : journal de la Société française de radiothérapie oncologique
  • [ISO-abbreviation] Cancer Radiother
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  •  go-up   go-down


55. Demiralp B, Ozdemir MT, Erler K, Basbozkurt M: Type 1 neurofibromatosis and adult extremity sarcoma. A report of two cases. Acta Orthop Belg; 2007 Jun;73(3):403-7
Genetic Alliance. consumer health - Neurofibromatosis type 1.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Type 1 neurofibromatosis and adult extremity sarcoma. A report of two cases.
  • We report two cases of malignant soft-tissue tumours--one myxoid malignant fibrous histiocytoma and one pleomorphic rhabdomyosarcoma--which were diagnosed in two young adult patients with type 1 neurofibromatosis (NF 1).
  • Diagnoses of myxoid malignant fibrous histiocytoma and pleomorphic rhabdomyosarcoma in adult NF 1 patients are exceedingly rare.
  • Thus detection of subtypes of rhabdomyosarcoma and malignant fibrous histiocytoma with immunohistochemistry may be helpful for the management of these tumours among other pleomorphic sarcomas that may occur in type 1 Neurofibromatosis.
  • [MeSH-major] Histiocytoma, Malignant Fibrous / complications. Neoplasms, Multiple Primary. Neurofibromatosis 1 / complications. Rhabdomyosarcoma / complications. Soft Tissue Neoplasms
  • [MeSH-minor] Adult. Humans. Male

  • Genetic Alliance. consumer health - Neurofibromatosis.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17715736.001).
  • [ISSN] 0001-6462
  • [Journal-full-title] Acta orthopaedica Belgica
  • [ISO-abbreviation] Acta Orthop Belg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Belgium
  •  go-up   go-down


56. Kaliaperumal S, Tiroumal S, Rao V: Orbital rhabdomyosarcoma: a case series. Indian J Cancer; 2007 Jul-Sep;44(3):104-7
Hazardous Substances Data Bank. DACTINOMYCIN .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Orbital rhabdomyosarcoma: a case series.
  • Orbital rhabdomyosarcoma is the most common orbital malignancy of childhood with the common presentation of rapidly evolving unilateral proptosis.
  • We studied six patients who were diagnosed and treated for rhabdomyosarcoma between January 1999 and June 2004.
  • Embryonal rhabdomyosarcoma was the commonest histopathological type in our series found in five patients.
  • [MeSH-major] Orbital Neoplasms / diagnosis. Rhabdomyosarcoma / diagnosis
  • [MeSH-minor] Adult. Antineoplastic Agents, Alkylating / therapeutic use. Child. Cyclophosphamide / therapeutic use. Dactinomycin / therapeutic use. Female. Humans. Male. Protein Synthesis Inhibitors / therapeutic use. Radiotherapy. Retrospective Studies

  • Hazardous Substances Data Bank. CYCLOPHOSPHAMIDE .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18250531.001).
  • [ISSN] 0019-509X
  • [Journal-full-title] Indian journal of cancer
  • [ISO-abbreviation] Indian J Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
  • [Chemical-registry-number] 0 / Antineoplastic Agents, Alkylating; 0 / Protein Synthesis Inhibitors; 1CC1JFE158 / Dactinomycin; 8N3DW7272P / Cyclophosphamide
  •  go-up   go-down


57. Huh WW, Beverly Raney R: Orbital metastasis in patients with rhabdomyosarcoma: case series and review of the literature. J Pediatr Hematol Oncol; 2006 Oct;28(10):684-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Orbital metastasis in patients with rhabdomyosarcoma: case series and review of the literature.
  • We present 3 cases of children who developed recurrent rhabdomyosarcoma with metastases to the orbit and review the medical literature.
  • Alveolar rhabdomyosarcoma was diagnosed in 7 cases.
  • [MeSH-major] Orbital Neoplasms / secondary. Pelvic Neoplasms / secondary. Rhabdomyosarcoma / secondary
  • [MeSH-minor] Adolescent. Adult. Child, Preschool. Disease Progression. Fatal Outcome. Female. Humans. Recurrence

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17023831.001).
  • [ISSN] 1077-4114
  • [Journal-full-title] Journal of pediatric hematology/oncology
  • [ISO-abbreviation] J. Pediatr. Hematol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 18
  •  go-up   go-down


58. Sheen-Chen SM, Eng HL, Ko SF: Metastatic rhabdomyosarcoma to the breast. Anticancer Res; 2005 Jan-Feb;25(1B):527-9
MedlinePlus Health Information. consumer health - Breast Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Metastatic rhabdomyosarcoma to the breast.
  • Although rhabdomyosarcoma is a common aggressive primary malignancy in the pediatric age group, metastatic deposits to the breast rarely occur and are mainly seen in adolescent girls.
  • Here, we report an intriguing, rare adult case with metastasis to the breast from nasal rhabdomyosarcoma.
  • Bilateral neck dissection was performed and rhabdomyosarcoma, metastatic to lymph node, was the final diagnosis.
  • [MeSH-major] Breast Neoplasms / diagnosis. Breast Neoplasms / secondary. Rhabdomyosarcoma / diagnosis. Rhabdomyosarcoma / pathology
  • [MeSH-minor] Actins / metabolism. Adult. Cell Nucleus / pathology. Female. Head and Neck Neoplasms / diagnosis. Head and Neck Neoplasms / pathology. Humans. Immunohistochemistry. Lymphatic Metastasis. Neoplasm Metastasis

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15816623.001).
  • [ISSN] 0250-7005
  • [Journal-full-title] Anticancer research
  • [ISO-abbreviation] Anticancer Res.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Greece
  • [Chemical-registry-number] 0 / Actins
  •  go-up   go-down


59. Scott RS, Jagirdar J: Right atrial botryoid rhabdomyosarcoma in an adult patient with recurrent pleomorphic rhabdomyosarcomas following doxorubicin therapy. Ann Diagn Pathol; 2007 Aug;11(4):274-6
Hazardous Substances Data Bank. DOXORUBICIN .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Right atrial botryoid rhabdomyosarcoma in an adult patient with recurrent pleomorphic rhabdomyosarcomas following doxorubicin therapy.
  • We describe a case of a 37-year-old Hispanic woman who presented with a right atrial botryoid rhabdomyosarcoma 2 years after doxorubicin therapy for a recurrent pleomorphic rhabdomyosarcoma of the chest wall.
  • [MeSH-major] Antibiotics, Antineoplastic / therapeutic use. Doxorubicin / therapeutic use. Heart Atria / pathology. Heart Neoplasms / pathology. Rhabdomyosarcoma, Embryonal / pathology
  • [MeSH-minor] Adult. Chemotherapy, Adjuvant. Disease-Free Survival. Female. Humans. Magnetic Resonance Imaging. Neoplasm Recurrence, Local. Thorax / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17630111.001).
  • [ISSN] 1092-9134
  • [Journal-full-title] Annals of diagnostic pathology
  • [ISO-abbreviation] Ann Diagn Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antibiotics, Antineoplastic; 80168379AG / Doxorubicin
  •  go-up   go-down


60. Kozakiewicz J, Gierlotka A, Dec M, Rolski J, Zuchowska-Vogelgesang B, Stockfish J: [The case of giant rhabdomyosarcoma of the head and neck and meagre symptomatology]. Otolaryngol Pol; 2010 Sep-Oct;64(5):328-30

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [The case of giant rhabdomyosarcoma of the head and neck and meagre symptomatology].
  • Histopathological examination revealed alveolar rhabdomyosarcoma.
  • [MeSH-major] Head / radiography. Neck / radiography. Parotid Neoplasms / radiography. Parotid Neoplasms / therapy. Rhabdomyosarcoma, Alveolar / radiography. Rhabdomyosarcoma, Alveolar / therapy
  • [MeSH-minor] Adult. Fatal Outcome. Female. Head and Neck Neoplasms / radiography. Head and Neck Neoplasms / therapy. Humans. Poland

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 21166146.001).
  • [ISSN] 0030-6657
  • [Journal-full-title] Otolaryngologia polska = The Polish otolaryngology
  • [ISO-abbreviation] Otolaryngol Pol
  • [Language] pol
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Poland
  •  go-up   go-down


61. Wu X, Li P, Xie L, Zhang X, Wang W, Xiao J, Wang F: [Clinical analysis of 13 cases of embryonal rhabdomyosarcoma in the nose]. Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2008 Apr;22(8):338-41
MedlinePlus Health Information. consumer health - Nasal Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Clinical analysis of 13 cases of embryonal rhabdomyosarcoma in the nose].
  • OBJECTIVE: To better understand the embryonal rhabdomyosarcoma of nose and make correct decision for diagnosis and treatment.
  • METHOD: Thirteen patients with rhabdomyosarcoma in the nose were studied retrospectively and the related literature was reviewed.
  • CONCLUSION: The pathological growth form of embryonal rhabdomyosarcoma in nose is often convert.
  • [MeSH-major] Nose Neoplasms. Rhabdomyosarcoma, Embryonal
  • [MeSH-minor] Adolescent. Adult. Child. Female. Humans. Male. Neoplasm Staging. Prognosis. Retrospective Studies. Young Adult

  • Genetic Alliance. consumer health - Rhabdomyosarcoma embryonal.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18595516.001).
  • [ISSN] 1001-1781
  • [Journal-full-title] Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery
  • [ISO-abbreviation] Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  •  go-up   go-down


62. Allende DS, Yang B: Primary ovarian rhabdomyosarcoma with heterologous elements: a case report. Int J Gynecol Pathol; 2008 Jul;27(3):402-6
MedlinePlus Health Information. consumer health - Ovarian Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary ovarian rhabdomyosarcoma with heterologous elements: a case report.
  • Primary ovarian rhabdomyosarcoma with heterologous elements is a rare ovarian neoplasm.
  • Pure primary rhabdomyosarcoma is extremely uncommon.
  • We present hereby a case of primary pure embryonal rhabdomyosarcoma in a 25-year-old woman, showing heterologous elements, but associated neither with teratoma nor with mixed mullerian tumors.
  • [MeSH-major] Ovarian Neoplasms / pathology. Rhabdomyosarcoma / pathology
  • [MeSH-minor] Adult. Female. Humans. Immunohistochemistry

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18580318.001).
  • [ISSN] 1538-7151
  • [Journal-full-title] International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists
  • [ISO-abbreviation] Int. J. Gynecol. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


63. Klem ML, Grewal RK, Wexler LH, Schöder H, Meyers PA, Wolden SL: PET for staging in rhabdomyosarcoma: an evaluation of PET as an adjunct to current staging tools. J Pediatr Hematol Oncol; 2007 Jan;29(1):9-14
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] PET for staging in rhabdomyosarcoma: an evaluation of PET as an adjunct to current staging tools.
  • BACKGROUND: Complete staging of rhabdomyosarcoma is critical to deliver appropriate therapy.
  • We evaluated the role of F-fluorodeoxyglucose positron emission tomography (PET) in the staging of patients with rhabdomyosarcoma.
  • METHODS: Twenty-four patients with rhabdomyosarcoma had a PET scan during staging evaluation, before or within 13 days of initiation of therapy.
  • CONCLUSIONS: These preliminary data indicate that PET is a useful adjunct in staging rhabdomyosarcoma.
  • A prospective study of PET for staging of rhabdomyosarcoma is warranted.
  • [MeSH-major] Neoplasm Staging. Positron-Emission Tomography. Rhabdomyosarcoma / radiography
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Evaluation Studies as Topic. Female. Fluorodeoxyglucose F18 / administration & dosage. Humans. Infant. Magnetic Resonance Imaging. Male. Middle Aged. Predictive Value of Tests. Radiopharmaceuticals / administration & dosage. Retrospective Studies. Sensitivity and Specificity. Tomography, X-Ray Computed

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17230060.001).
  • [ISSN] 1077-4114
  • [Journal-full-title] Journal of pediatric hematology/oncology
  • [ISO-abbreviation] J. Pediatr. Hematol. Oncol.
  • [Language] eng
  • [Publication-type] Clinical Trial; Comparative Study; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Radiopharmaceuticals; 0Z5B2CJX4D / Fluorodeoxyglucose F18
  •  go-up   go-down


64. Tavil Y, Turkoglu S, Tacoy G, Cemri M: Huge biatrial cardiac rhabdomyosarcoma resulting in bilateral atrioventricular valve obstruction. Cardiovasc Pathol; 2006 Nov-Dec;15(6):354-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Huge biatrial cardiac rhabdomyosarcoma resulting in bilateral atrioventricular valve obstruction.
  • Cardiac rhabdomyosarcoma (CR) is extremely rare in adult patients.
  • [MeSH-major] Heart Atria / pathology. Heart Neoplasms / pathology. Heart Valves / pathology. Rhabdomyosarcoma / secondary. Ventricular Outflow Obstruction / pathology
  • [MeSH-minor] Adult. Antineoplastic Protocols. Biopsy. Echocardiography. Fatal Outcome. Humans. Male. Palliative Care. Tomography, X-Ray Computed

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17113015.001).
  • [ISSN] 1054-8807
  • [Journal-full-title] Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology
  • [ISO-abbreviation] Cardiovasc. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


65. Stock N, Chibon F, Binh MB, Terrier P, Michels JJ, Valo I, Robin YM, Guillou L, Ranchère-Vince D, Decouvelaere AV, Collin F, Birtwisle-Peyrottes I, Gregoire F, Aurias A, Coindre JM: Adult-type rhabdomyosarcoma: analysis of 57 cases with clinicopathologic description, identification of 3 morphologic patterns and prognosis. Am J Surg Pathol; 2009 Dec;33(12):1850-9
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult-type rhabdomyosarcoma: analysis of 57 cases with clinicopathologic description, identification of 3 morphologic patterns and prognosis.
  • Adult-type rhabdomyosarcoma (RMS) has been classically defined as a pleomorphic sarcoma with desmin expression occurring in adult patients.
  • In conclusion, adult-type RMS is a rare sarcoma occurring mainly in the extremities and trunk wall with 2 main histologic patterns, spindle cell, and pleomorphic patterns, which represent the end of the spectrum of a single entity.
  • [MeSH-major] Rhabdomyosarcoma / pathology. Soft Tissue Neoplasms / pathology
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Biomarkers, Tumor / analysis. Biomarkers, Tumor / genetics. Comparative Genomic Hybridization. Diagnosis, Differential. Disease-Free Survival. Female. Gene Expression Regulation, Neoplastic. Humans. Immunohistochemistry. Immunophenotyping. In Situ Hybridization, Fluorescence. Kaplan-Meier Estimate. Male. Middle Aged. Neoplasm Recurrence, Local. Neoplasm Staging. Predictive Value of Tests. Time Factors. Treatment Outcome. Young Adult

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19898221.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
  •  go-up   go-down


66. Martorell M, Ortiz CM, Garcia JA: Testicular fusocellular rhabdomyosarcoma as a metastasis of elbow sclerosing rhabdomyosarcoma: A clinicopathologic, immunohistochemical and molecular study of one case. Diagn Pathol; 2010;5:52
NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Testicular fusocellular rhabdomyosarcoma as a metastasis of elbow sclerosing rhabdomyosarcoma: A clinicopathologic, immunohistochemical and molecular study of one case.
  • Sclerosing rhabdomyosarcoma (SRMS) is an infrequent variant of rhabdomyosarcoma characterized by extensive intercellular hyaline fibrosis.
  • Histologically, the tumor showed an abundant extracellular hyaline matrix with extratumoral vascular emboli and microscopic foci of fusocellular embryonal rhabdomyosarcoma (FRMS) separated by a fibrotic band from the sclerosing areas.
  • [MeSH-major] Rhabdomyosarcoma, Embryonal / secondary. Soft Tissue Neoplasms / pathology. Testicular Neoplasms / secondary
  • [MeSH-minor] Adult. Biomarkers, Tumor / analysis. Biomarkers, Tumor / genetics. Chemotherapy, Adjuvant. Chromosomes, Human, Pair 13. Elbow. Fatal Outcome. Fibrosis. Forkhead Transcription Factors / genetics. Humans. Immunohistochemistry. In Situ Hybridization, Fluorescence. Male. Orchiectomy. Sclerosis. Time Factors. Tomography, X-Ray Computed. Translocation, Genetic. Treatment Outcome. Whole Body Imaging

  • MedlinePlus Health Information. consumer health - Testicular Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Virchows Arch. 2000 Apr;436(4):305-11 [10834531.001]
  • [Cites] Int J Surg Pathol. 2010 Oct;18(5):394-7 [19017660.001]
  • [Cites] Am J Surg Pathol. 2002 Sep;26(9):1175-83 [12218574.001]
  • [Cites] J Pediatr Surg. 2003 Aug;38(8):E1-3 [12891513.001]
  • [Cites] Prog Urol. 2003 Sep;13(4):700-2 [14650311.001]
  • [Cites] Pediatr Dev Pathol. 2004 Jul-Aug;7(4):391-6 [15383934.001]
  • [Cites] Cancer. 1990 Jun 1;65(11):2611-4 [2337879.001]
  • [Cites] Laryngoscope. 2005 Jan;115(1):48-50 [15630365.001]
  • [Cites] Pediatr Dev Pathol. 2004 Nov-Dec;7(6):583-94 [15630526.001]
  • [Cites] Virchows Arch. 2005 Jan;446(1):64-7 [15660283.001]
  • [Cites] Am J Surg Pathol. 2005 Aug;29(8):1106-13 [16006807.001]
  • [Cites] Int J Surg Pathol. 2006 Jul;14(3):193-9 [16959698.001]
  • [Cites] Arch Pathol Lab Med. 2006 Oct;130(10):1454-65 [17090187.001]
  • [Cites] Virchows Arch. 2006 Nov;449(5):554-60 [17013628.001]
  • [Cites] Virchows Arch. 2006 Nov;449(5):572-8 [17016719.001]
  • [Cites] Am J Clin Pathol. 2008 Mar;129(3):410-5 [18285263.001]
  • [Cites] Virchows Arch. 2008 Mar;452(3):251-8 [18094995.001]
  • [Cites] Ann Diagn Pathol. 2009 Oct;13(5):334-8 [19751910.001]
  • [Cites] Pathologe. 2010 Mar;31(2):91-6 [19997735.001]
  • [Cites] Histopathology. 2000 Oct;37(4):323-31 [11012739.001]
  • (PMID = 20701800.001).
  • [ISSN] 1746-1596
  • [Journal-full-title] Diagnostic pathology
  • [ISO-abbreviation] Diagn Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / FOXO1 protein, human; 0 / Forkhead Transcription Factors
  • [Other-IDs] NLM/ PMC3224966
  •  go-up   go-down


67. Gupta A, Sharma MC, Kochupillai V, Kichendasse G, Gupta A, Atri S, Medhi K: Primary pulmonary rhabdomyosarcoma in adults: case report and review of literature. Clin Lung Cancer; 2007 May;8(6):389-91
MedlinePlus Health Information. consumer health - Lung Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Primary pulmonary rhabdomyosarcoma in adults: case report and review of literature.
  • On histopathologic examination, a diagnosis of pleiomorphic rhabdomyosarcoma stage III of the lung was made.
  • Chemotherapy using IRS (Intergroup Rhabdomyosarcoma Study) IV protocol with radiation therapy (RT) at week 9 was planned.
  • [MeSH-major] Lung Neoplasms / pathology. Rhabdomyosarcoma / pathology
  • [MeSH-minor] Adult. Antineoplastic Agents / therapeutic use. Combined Modality Therapy. Diaphragm / pathology. Fatal Outcome. Humans. Male. Pericardium / pathology. Radiotherapy. Tomography, X-Ray Computed

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17562241.001).
  • [ISSN] 1525-7304
  • [Journal-full-title] Clinical lung cancer
  • [ISO-abbreviation] Clin Lung Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antineoplastic Agents
  •  go-up   go-down


68. Wu HY, Snyder HM 3rd, Womer RB: Genitourinary rhabdomyosarcoma: which treatment, how much, and when? J Pediatr Urol; 2009 Dec;5(6):501-6
NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Genitourinary rhabdomyosarcoma: which treatment, how much, and when?
  • OBJECTIVE: To review the current management of pediatric genitourinary rhabdomyosarcoma (RMS).
  • METHODS: Studies performed by the Intergroup Rhabdomyosarcoma Study Group, Children's Oncology Group (COG), International Society of Paediatric Oncology (SIOP) and others over the past 10 years were reviewed to compare the use of surgery, chemotherapy, and radiotherapy for treatment of RMS and their associated outcomes.
  • [MeSH-major] Rhabdomyosarcoma / therapy. Urogenital Neoplasms / therapy
  • [MeSH-minor] Adolescent. Child. Child, Preschool. Humans. Infant. Young Adult

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19640790.001).
  • [ISSN] 1873-4898
  • [Journal-full-title] Journal of pediatric urology
  • [ISO-abbreviation] J Pediatr Urol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 37
  •  go-up   go-down


69. Moretti G, Guimarães R, Oliveira KM, Sanjar F, Voegels RL: Rhabdomyosarcoma of the head and neck: 24 cases and literature review. Braz J Otorhinolaryngol; 2010 Jul-Aug;76(4):533-7
MedlinePlus Health Information. consumer health - Head and Neck Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rhabdomyosarcoma of the head and neck: 24 cases and literature review.
  • Rhabdomyosarcoma (RMS) is a malignant tumor of soft tissues, more common in childhood, mainly located in the head and neck.
  • MATERIALS AND METHODS: A retrospective analysis of data from 24 patients with head and neck rhabdomyosarcoma diagnosed and treated in a hospital from 1994 to 2008.
  • [MeSH-major] Head and Neck Neoplasms. Rhabdomyosarcoma
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Combined Modality Therapy / methods. Disease-Free Survival. Female. Humans. Infant. Infant, Newborn. Male. Middle Aged. Retrospective Studies. Young Adult

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20835543.001).
  • [ISSN] 1808-8686
  • [Journal-full-title] Brazilian journal of otorhinolaryngology
  • [ISO-abbreviation] Braz J Otorhinolaryngol
  • [Language] eng; por
  • [Publication-type] Journal Article; Review
  • [Publication-country] Brazil
  •  go-up   go-down


70. Li SR, Yang ZY, Zheng SY: [Appearance and clinical value of MRI in sinonasal embryonal rhabdomyosarcoma]. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2010 May;45(5):393-6
MedlinePlus Health Information. consumer health - MRI Scans.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Appearance and clinical value of MRI in sinonasal embryonal rhabdomyosarcoma].
  • OBJECTIVE: To investigate the appearance and clinical value of MRI in the diagnosis of embryonal rhabdomyosarcoma in nasal cavity and paranasal sinuses.
  • METHODS: The clinical, pathological and MRI findings of five patients with pathology proved embryonal rhabdomyosarcoma in nasal cavity and paranasal sinuses were retrospectively analyzed.
  • CONCLUSIONS: There are some special MRI findings in embryonal rhabdomyosarcoma located in nasal cavity and paranasal sinuses.
  • [MeSH-major] Magnetic Resonance Imaging. Paranasal Sinus Neoplasms / diagnosis. Rhabdomyosarcoma, Embryonal / diagnosis
  • [MeSH-minor] Adolescent. Adult. Child. Female. Humans. Male. Nasal Cavity. Retrospective Studies. Young Adult

  • Genetic Alliance. consumer health - Rhabdomyosarcoma embryonal.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20654175.001).
  • [ISSN] 1673-0860
  • [Journal-full-title] Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
  • [ISO-abbreviation] Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
  • [Language] chi
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] China
  •  go-up   go-down


71. Amin RM, Kokubo T, Hiroshima K, Narita M, Itou K, Kuroki M, Tanizawa T, Nakatani Y: Metastatic germ cell tumor of the lung masquerading as primary rhabdomyosarcoma. Pathol Int; 2005 Oct;55(10):649-54
MedlinePlus Health Information. consumer health - Testicular Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Metastatic germ cell tumor of the lung masquerading as primary rhabdomyosarcoma.
  • Video-assisted thoracoscopic partial resection of the tumor revealed a 24 x 20 mm teratoma with somatic-type malignancy in which pleomorphic rhabdomyosarcoma was a major element.
  • One year later, asymptomatic tumor recurrence occurred at both edges of the stapler line as 22 x 20 mm and 10 x 5 mm nodules composed only of pleomorphic rhabdomyosarcoma.
  • [MeSH-major] Lung Neoplasms / diagnosis. Neoplasms, Germ Cell and Embryonal / diagnosis. Rhabdomyosarcoma / diagnosis. Testicular Neoplasms / diagnosis
  • [MeSH-minor] Adult. Biomarkers, Tumor / analysis. Chemotherapy, Adjuvant. Combined Modality Therapy. Diagnosis, Differential. Humans. Immunoenzyme Techniques. Male. Neoplasm Recurrence, Local. Tomography, X-Ray Computed

  • MedlinePlus Health Information. consumer health - Lung Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16185296.001).
  • [ISSN] 1320-5463
  • [Journal-full-title] Pathology international
  • [ISO-abbreviation] Pathol. Int.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Australia
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
  •  go-up   go-down


72. Moon HS, Kwon SW, Lee JH: A case of alveolar rhabdomyosarcoma of the ethmoid sinus invading the orbit in an adult. Korean J Ophthalmol; 2006 Mar;20(1):70-5
Genetic Alliance. consumer health - Rhabdomyosarcoma alveolar.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A case of alveolar rhabdomyosarcoma of the ethmoid sinus invading the orbit in an adult.
  • PURPOSE: A case study and literature review of alveolar rhabdomyosarcoma (RMS) in an adult.
  • [MeSH-major] Ethmoid Sinus. Orbital Neoplasms / pathology. Paranasal Sinus Neoplasms / pathology. Rhabdomyosarcoma, Alveolar / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Cancer. 2001 Feb 15;91(4):794-803 [11241248.001]
  • [Cites] Virchows Arch Pathol Anat Physiol Klin Med. 1962;335:329-44 [14488094.001]
  • [Cites] Ann Surg. 2001 Aug;234(2):215-23 [11505068.001]
  • [Cites] Ophthalmology. 2001 Dec;108(12):2284-92 [11733272.001]
  • [Cites] Trans Am Ophthalmol Soc. 2001;99:133-42; discussion 142-3 [11797301.001]
  • [Cites] Cancer. 2002 Jul 15;95(2):377-88 [12124838.001]
  • [Cites] Surv Ophthalmol. 2003 Jan-Feb;48(1):39-57 [12559326.001]
  • [Cites] Cancer Control. 2004 Sep-Oct;11(5):328-33 [15377992.001]
  • [Cites] Laryngoscope. 1975 Feb;85(2):400-10 [46581.001]
  • [Cites] J Oral Maxillofac Surg. 1988 Dec;46(12):1090-6 [3057148.001]
  • [Cites] Ophthal Plast Reconstr Surg. 1994 Dec;10(4):283-6 [7865452.001]
  • [Cites] J Clin Oncol. 1995 Mar;13(3):610-30 [7884423.001]
  • [Cites] Clin Imaging. 1995 Oct-Dec;19(4):234-6 [8564864.001]
  • [Cites] Clin Radiol. 1998 May;53(5):357-62 [9630275.001]
  • [Cites] Cancer. 1958 Jan-Feb;11(1):181-99 [13500314.001]
  • [Cites] J Clin Oncol. 2001 Jun 15;19(12):3091-102 [11408506.001]
  • (PMID = 16768194.001).
  • [ISSN] 1011-8942
  • [Journal-full-title] Korean journal of ophthalmology : KJO
  • [ISO-abbreviation] Korean J Ophthalmol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Korea (South)
  • [Other-IDs] NLM/ PMC2908821
  •  go-up   go-down


73. Rodríguez García N, Llanes González L, Pascual Mateo C, Berenguer Sánchez A: [Spermatic cord rhabdomyosarcoma in an adult]. Arch Esp Urol; 2005 Nov;58(9):956-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Spermatic cord rhabdomyosarcoma in an adult].
  • OBJECTIVES: To report one case of spermatic cord rabdomyosarcoma in an adult patient.
  • [MeSH-major] Genital Neoplasms, Male. Rhabdomyosarcoma. Spermatic Cord
  • [MeSH-minor] Adult. Humans. Male

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16430046.001).
  • [ISSN] 0004-0614
  • [Journal-full-title] Archivos españoles de urología
  • [ISO-abbreviation] Arch. Esp. Urol.
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
  •  go-up   go-down


74. Mentzel T, Kuhnen C: Spindle cell rhabdomyosarcoma in adults: clinicopathological and immunohistochemical analysis of seven new cases. Virchows Arch; 2006 Nov;449(5):554-60
MedlinePlus Health Information. consumer health - Soft Tissue Sarcoma.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Spindle cell rhabdomyosarcoma in adults: clinicopathological and immunohistochemical analysis of seven new cases.
  • Rhabdomyosarcoma (RMS) is currently classified into embryonal RMS, including its botryoid and spindle cell variants, alveolar RMS, including a solid variant, and pleomorphic RMS.
  • We analysed the clinicopathological and immunohistochemical features of seven new cases of spindle cell RMS arising in adult patients.
  • In summary, spindle cell rhabdomyosarcoma represents a rare neoplasm in adulthood characterized clinically by a rather poor prognosis, and shows a broad morphological spectrum including most likely the sclerosing, pseudovascular variant.
  • [MeSH-major] Rhabdomyosarcoma / pathology. Sarcoma / pathology. Soft Tissue Neoplasms / pathology
  • [MeSH-minor] Adult. Aged. Antigens, CD / analysis. Cell Adhesion Molecules / analysis. Female. Humans. Immunohistochemistry. Male. Middle Aged

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17013628.001).
  • [ISSN] 0945-6317
  • [Journal-full-title] Virchows Archiv : an international journal of pathology
  • [ISO-abbreviation] Virchows Arch.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Antigens, CD; 0 / CD99 protein, human; 0 / Cell Adhesion Molecules
  •  go-up   go-down


75. Kobayashi S, Tsukamoto T, Tohma T: [A case of metastatic paratesticular rhabdomyosarcoma in an adult successfully treated with multidrug combination chemotherapy]. Hinyokika Kiyo; 2010 Sep;56(9):531-3
Hazardous Substances Data Bank. VINCRISTINE .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [A case of metastatic paratesticular rhabdomyosarcoma in an adult successfully treated with multidrug combination chemotherapy].
  • He underwent left high orchiectomy and was diagnosed with paratesticular embryonal rhabdomyosarcoma.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Genital Neoplasms, Male / drug therapy. Rhabdomyosarcoma, Embryonal / drug therapy
  • [MeSH-minor] Cyclophosphamide / therapeutic use. Dacarbazine / therapeutic use. Doxorubicin / therapeutic use. Humans. Lung Neoplasms / secondary. Lymphatic Metastasis. Male. Testis. Vincristine / therapeutic use. Young Adult

  • Hazardous Substances Data Bank. DOXORUBICIN .
  • Hazardous Substances Data Bank. DACARBAZINE .
  • Hazardous Substances Data Bank. CYCLOPHOSPHAMIDE .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20940531.001).
  • [ISSN] 0018-1994
  • [Journal-full-title] Hinyokika kiyo. Acta urologica Japonica
  • [ISO-abbreviation] Hinyokika Kiyo
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Japan
  • [Chemical-registry-number] 5J49Q6B70F / Vincristine; 7GR28W0FJI / Dacarbazine; 80168379AG / Doxorubicin; 8N3DW7272P / Cyclophosphamide; CYVADIC protocol
  •  go-up   go-down


76. Lindén O, Greiff L, Wahlberg P, Vinge E, Kjellén E: Chemorefractory rhabdomyosarcoma treated with radiotherapy, bevacizumab, statins and surgery and maintenance with bevacizumab and chemotherapy. Onkologie; 2008 Jul;31(7):391-3
MedlinePlus Health Information. consumer health - Statins.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Chemorefractory rhabdomyosarcoma treated with radiotherapy, bevacizumab, statins and surgery and maintenance with bevacizumab and chemotherapy.
  • BACKGROUND: Rhabdomyosarcoma is a rare disease in children and young adults, usually responsive to chemotherapy.
  • CASE REPORT: A young woman presented with an embryonal rhabdomyosarcoma of the retromaxillary space.
  • CONCLUSION: Rhabdomyosarcoma refractory to chemotherapy may respond to radiotherapy and the addition of bevacizumab and statins.
  • [MeSH-major] Antibodies, Monoclonal / administration & dosage. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Hydroxymethylglutaryl-CoA Reductase Inhibitors / administration & dosage. Maxillary Neoplasms / therapy. Oral Surgical Procedures. Radiotherapy / methods. Rhabdomyosarcoma / therapy
  • [MeSH-minor] Adult. Antibodies, Monoclonal, Humanized. Bevacizumab. Combined Modality Therapy. Female. Humans. Radiotherapy, Adjuvant. Treatment Outcome

  • MedlinePlus Health Information. consumer health - Radiation Therapy.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Copyright] (c) 2008 S. Karger AG, Basel
  • (PMID = 18596387.001).
  • [ISSN] 1423-0240
  • [Journal-full-title] Onkologie
  • [ISO-abbreviation] Onkologie
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Switzerland
  • [Chemical-registry-number] 0 / Antibodies, Monoclonal; 0 / Antibodies, Monoclonal, Humanized; 0 / Hydroxymethylglutaryl-CoA Reductase Inhibitors; 2S9ZZM9Q9V / Bevacizumab
  •  go-up   go-down


77. Papacharalampous GX, Manolopoulos L, Korres S, Dicoglou C, Bibas A: Adult laryngeal rhabdomyosarcoma: is aggressive treatment justified in all cases? A case report and review of the literature. J Laryngol Otol; 2009 Nov;123(11):e21

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Adult laryngeal rhabdomyosarcoma: is aggressive treatment justified in all cases? A case report and review of the literature.
  • BACKGROUND: Adult laryngeal rhabdomyosarcomas are rare tumours commonly treated by laryngectomy.
  • CASE REPORT: We present a case of subglottic laryngeal rhabdomyosarcoma in an elderly woman, treated by endoscopic resection.
  • [MeSH-major] Laryngeal Neoplasms / surgery. Microsurgery / methods. Rhabdomyosarcoma / surgery

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19719884.001).
  • [ISSN] 1748-5460
  • [Journal-full-title] The Journal of laryngology and otology
  • [ISO-abbreviation] J Laryngol Otol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 33
  •  go-up   go-down


78. França CM, Caran EM, Alves MT, Barreto AD, Lopes NN: Rhabdomyosarcoma of the oral tissues--two new cases and literature review. Med Oral Patol Oral Cir Bucal; 2006 Mar;11(2):E136-40
MedlinePlus Health Information. consumer health - Oral Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Rhabdomyosarcoma of the oral tissues--two new cases and literature review.
  • Rhabdomyosarcoma (RMS) is a malignant soft tissue neoplasm consisting of cells derived from the primitive mesenchyme that exhibit a profound tendency to myogenesis.
  • [MeSH-major] Mouth Neoplasms. Rhabdomyosarcoma
  • [MeSH-minor] Adolescent. Adult. Fatal Outcome. Female. Humans. Male

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16505791.001).
  • [ISSN] 1698-6946
  • [Journal-full-title] Medicina oral, patología oral y cirugía bucal
  • [ISO-abbreviation] Med Oral Patol Oral Cir Bucal
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Spain
  • [Number-of-references] 15
  •  go-up   go-down


79. Li G, Ogose A, Kawashima H, Umezu H, Hotta T, Tohyama T, Ariizumi T, Endo N: Cytogenetic and real-time quantitative reverse-transcriptase polymerase chain reaction analyses in pleomorphic rhabdomyosarcoma. Cancer Genet Cytogenet; 2009 Jul;192(1):1-9
MedlinePlus Health Information. consumer health - Bone Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cytogenetic and real-time quantitative reverse-transcriptase polymerase chain reaction analyses in pleomorphic rhabdomyosarcoma.
  • Pleomorphic rhabdomyosarcoma (PRMS) is a rare variant of rhabdomyosarcoma that occurs mostly in adults.
  • We herein report a cytogenetic study of three cases of pleomorphic rhabdomyosarcoma using a conventional G-banded karyotyping analysis.
  • [MeSH-major] Abdominal Neoplasms / diagnosis. Bone Neoplasms / diagnosis. Cytogenetic Analysis / methods. Reverse Transcriptase Polymerase Chain Reaction / methods. Rhabdomyosarcoma / diagnosis
  • [MeSH-minor] Adult. Aged. Aged, 80 and over. Diagnosis, Differential. Female. Humans. Male. Middle Aged. Retrospective Studies

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19480930.001).
  • [ISSN] 1873-4456
  • [Journal-full-title] Cancer genetics and cytogenetics
  • [ISO-abbreviation] Cancer Genet. Cytogenet.
  • [Language] eng
  • [Publication-type] Case Reports; Evaluation Studies; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


80. Pazzaglia L, Chiechi A, Conti A, Gamberi G, Magagnoli G, Novello C, Morandi L, Picci P, Mercuri M, Benassi MS: Genetic and molecular alterations in rhabdomyosarcoma: mRNA overexpression of MCL1 and MAP2K4 genes. Histol Histopathol; 2009 01;24(1):61-7
NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Genetic and molecular alterations in rhabdomyosarcoma: mRNA overexpression of MCL1 and MAP2K4 genes.
  • Rhabdomyosarcoma, the most common soft tissue sarcoma in childhood, belongs to the small round cell tumor family and is classified according to its histopathological features as embryonal, alveolar and pleomorphic.
  • In this study we propose to explore genetic alterations involved in rhabdomyosarcoma tumorigenesis and assess the level of mRNA gene expression of controlling survival signalling pathways.
  • Our findings on rhabdomyosarcoma samples showed multiple copy number alterations in chromosome regions implicated in malignancy progression and indicated a strong expression of MAP2K4 and MCL1 genes, both involved in different biological functions of complicated signalling pathways.
  • [MeSH-major] MAP Kinase Kinase 4 / genetics. Proto-Oncogene Proteins c-bcl-2 / genetics. RNA, Messenger / analysis. Rhabdomyosarcoma / genetics. Soft Tissue Neoplasms / genetics
  • [MeSH-minor] Adolescent. Adult. Aged. Child, Preschool. Comparative Genomic Hybridization. Female. Gene Dosage. Gene Expression. Humans. Image Interpretation, Computer-Assisted. Male. Middle Aged. Myeloid Cell Leukemia Sequence 1 Protein. Oligonucleotide Array Sequence Analysis. Reverse Transcriptase Polymerase Chain Reaction

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19012245.001).
  • [ISSN] 1699-5848
  • [Journal-full-title] Histology and histopathology
  • [ISO-abbreviation] Histol. Histopathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Spain
  • [Chemical-registry-number] 0 / Myeloid Cell Leukemia Sequence 1 Protein; 0 / Proto-Oncogene Proteins c-bcl-2; 0 / RNA, Messenger; EC 2.7.12.2 / MAP Kinase Kinase 4; EC 2.7.12.2 / MAP2K4 protein, human
  •  go-up   go-down


81. Leung F, Terzibachian JJ, Ramanah R, Govyadovskiy A, Aouar Z, Lassabe C, Riethmuller D: [Pure rhabdomyosarcoma of the uterine corpus: an exceptional tumor in postmenopausal women. Report on two cases]. J Gynecol Obstet Biol Reprod (Paris); 2009 Feb;38(1):72-6
MedlinePlus Health Information. consumer health - Vaginal Bleeding.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Pure rhabdomyosarcoma of the uterine corpus: an exceptional tumor in postmenopausal women. Report on two cases].
  • Rhabdomyosarcoma (RMS) of the uterine corpus is rare in adult females.
  • This tumor can be encountered in two distinct histopathological contexts: usually as a component of a malignant mixed mullerian tumor and exceptionally as a pure heterologous sarcoma.
  • [MeSH-major] Rhabdomyosarcoma / diagnosis. Uterine Hemorrhage / etiology. Uterine Neoplasms / diagnosis

  • MedlinePlus Health Information. consumer health - Uterine Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19111997.001).
  • [ISSN] 0368-2315
  • [Journal-full-title] Journal de gynécologie, obstétrique et biologie de la reproduction
  • [ISO-abbreviation] J Gynecol Obstet Biol Reprod (Paris)
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  •  go-up   go-down


82. Esfahani SA, Montaser-Kouhsari L, Saeedi P, Sadeghi Z, Kajbafzadeh AM: An antenatally diagnosed rhabdomyosarcoma of the bladder treated without extensive surgery. Nat Rev Urol; 2009 Aug;6(8):449-53
MedlinePlus Health Information. consumer health - Uncommon Infant and Newborn Problems.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] An antenatally diagnosed rhabdomyosarcoma of the bladder treated without extensive surgery.
  • DIAGNOSIS: Botryoid subtype of rhabdomyosarcoma occupying most of the bladder and protruding through the urethra, with bilateral hydroureteronephrosis.
  • [MeSH-major] Infant, Newborn, Diseases / therapy. Prenatal Diagnosis. Rhabdomyosarcoma / diagnosis. Rhabdomyosarcoma / therapy. Urinary Bladder Neoplasms / diagnosis. Urinary Bladder Neoplasms / therapy
  • [MeSH-minor] Antineoplastic Agents / therapeutic use. Female. Humans. Infant, Newborn. Pregnancy. Treatment Outcome. Young Adult


83. Wang S, Guo L, Dong L, Guo L, Li S, Zhang J, Sun M: TGF-beta1 signal pathway may contribute to rhabdomyosarcoma development by inhibiting differentiation. Cancer Sci; 2010 May;101(5):1108-16
NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] TGF-beta1 signal pathway may contribute to rhabdomyosarcoma development by inhibiting differentiation.
  • Overexpression of transforming growth factor-beta1 (TGF-beta1) and its downstream molecules in the rhabdomyosarcoma (RMS) RD cell line has been reported previously, but the regulatory role of TGF-beta1 on RMS has not been studied extensively.
  • Moreover, a proportion of treated rhabdomyosarcoma (RD) cells changed to a round shape from the normal fusiform or polygonal shape and expressed myofilaments.
  • [MeSH-major] Rhabdomyosarcoma / etiology. Signal Transduction / physiology. Transforming Growth Factor beta1 / physiology
  • [MeSH-minor] Adolescent. Adult. Cell Differentiation. Child. Child, Preschool. Female. Humans. Infant. Male. Protein-Serine-Threonine Kinases / analysis. RNA Interference. Receptors, Transforming Growth Factor beta / analysis. Smad4 Protein / analysis

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20219075.001).
  • [ISSN] 1349-7006
  • [Journal-full-title] Cancer science
  • [ISO-abbreviation] Cancer Sci.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Receptors, Transforming Growth Factor beta; 0 / SMAD4 protein, human; 0 / Smad4 Protein; 0 / Transforming Growth Factor beta1; EC 2.7.11.1 / Protein-Serine-Threonine Kinases; EC 2.7.11.30 / transforming growth factor-beta type II receptor
  •  go-up   go-down


84. Meazza C, Casanova M, Zaffignani E, Luksch R, Podda M, Favini F, Catania S, Biassoni V, Morosi C, Ferrari A: Efficacy of topotecan plus vincristine and doxorubicin in children with recurrent/refractory rhabdomyosarcoma. Med Oncol; 2009;26(1):67-72
Hazardous Substances Data Bank. VINCRISTINE .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Efficacy of topotecan plus vincristine and doxorubicin in children with recurrent/refractory rhabdomyosarcoma.
  • BACKGROUND: This study investigates the efficacy and the feasibility of a chemotherapy regimen with topotecan plus vincristine and doxorubicin (TVD) given on an individually tailored basis to patients with refractory/recurrent rhabdomyosarcoma (RMS).
  • [MeSH-major] Doxorubicin / administration & dosage. Rhabdomyosarcoma / drug therapy. Topotecan / administration & dosage. Vincristine / administration & dosage
  • [MeSH-minor] Adolescent. Adult. Antibiotics, Antineoplastic / administration & dosage. Antibiotics, Antineoplastic / adverse effects. Antineoplastic Agents, Phytogenic / administration & dosage. Antineoplastic Agents, Phytogenic / adverse effects. Antineoplastic Combined Chemotherapy Protocols / administration & dosage. Antineoplastic Combined Chemotherapy Protocols / adverse effects. Child. Child, Preschool. Drug Administration Schedule. Female. Humans. Infusions, Intravenous. Male. Neoplasm Recurrence, Local. Treatment Outcome

  • Hazardous Substances Data Bank. Topotecan .
  • Hazardous Substances Data Bank. DOXORUBICIN .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18679836.001).
  • [ISSN] 1357-0560
  • [Journal-full-title] Medical oncology (Northwood, London, England)
  • [ISO-abbreviation] Med. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antibiotics, Antineoplastic; 0 / Antineoplastic Agents, Phytogenic; 5J49Q6B70F / Vincristine; 7M7YKX2N15 / Topotecan; 80168379AG / Doxorubicin
  •  go-up   go-down


85. Wolden SL, Wexler LH, Kraus DH, Laquaglia MP, Lis E, Meyers PA: Intensity-modulated radiotherapy for head-and-neck rhabdomyosarcoma. Int J Radiat Oncol Biol Phys; 2005 Apr 1;61(5):1432-8
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Intensity-modulated radiotherapy for head-and-neck rhabdomyosarcoma.
  • PURPOSE: To determine the preliminary results of intensity-modulated radiotherapy (IMRT) for head-and-neck rhabdomyosarcoma.
  • Acute radiation toxicity was similar to that reported by the Intergroup Rhabdomyosarcoma Study Group.
  • [MeSH-major] Head and Neck Neoplasms / radiotherapy. Radiotherapy, Conformal / methods. Rhabdomyosarcoma / radiotherapy
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Female. Humans. Infant. Male. Radiotherapy Dosage

  • MedlinePlus Health Information. consumer health - Head and Neck Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [CommentIn] Int J Radiat Oncol Biol Phys. 2005 Oct 1;63(2):647-8; author reply 648-9 [16168860.001]
  • (PMID = 15817347.001).
  • [ISSN] 0360-3016
  • [Journal-full-title] International journal of radiation oncology, biology, physics
  • [ISO-abbreviation] Int. J. Radiat. Oncol. Biol. Phys.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


86. Meazza C, Ferrari A, Casanova M, Gandola L, Collini P, Massimino M, Luksch R, Spreafico F, Cefalo G, Polastri D, Terenziani M, Podda M, Cantù G, Scaramuzza D, Fossati-Bellani F: Evolving treatment strategies for parameningeal rhabdomyosarcoma: the experience of the Istituto Nazionale Tumori of Milan. Head Neck; 2005 Jan;27(1):49-57

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Evolving treatment strategies for parameningeal rhabdomyosarcoma: the experience of the Istituto Nazionale Tumori of Milan.
  • BACKGROUND: Ninety pediatric patients with parameningeal rhabdomyosarcoma (PM-RMS) were treated between 1970 and 2002 at the Istituto Nazionale Tumori, Milan.
  • [MeSH-major] Meningeal Neoplasms / therapy. Neoplasms, Unknown Primary / therapy. Rhabdomyosarcoma / therapy
  • [MeSH-minor] Adolescent. Adult. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Brain Neoplasms / prevention & control. Chemotherapy, Adjuvant. Child. Child, Preschool. Cranial Irradiation. Dose Fractionation. Female. Humans. Infant. Italy / epidemiology. Male. Neoplasm Recurrence, Local. Radiotherapy, Adjuvant. Treatment Outcome

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Copyright] Copyright 2004 Wiley Periodicals, Inc.
  • (PMID = 15529318.001).
  • [ISSN] 1043-3074
  • [Journal-full-title] Head & neck
  • [ISO-abbreviation] Head Neck
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


87. Klijanienko J, Caillaud JM, Orbach D, Brisse H, Lagacé R, Vielh P, Couturier J, Fréneaux P, Theocharis S, Sastre-Garau X: Cyto-histological correlations in primary, recurrent and metastatic rhabdomyosarcoma: the institut Curie's experience. Diagn Cytopathol; 2007 Aug;35(8):482-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cyto-histological correlations in primary, recurrent and metastatic rhabdomyosarcoma: the institut Curie's experience.
  • To determine diagnostic cytomorphologic features of rhabdomyosarcoma (RMS) on fine-needle aspiration (FNA) material, the cytologic material and corresponding histologic slides of 180 tumors obtained from 109 patients were reviewed.
  • A review of original cytology reports revealed that 176 of 180 (97.8%) tumors were either diagnosed accurately or as round cell sarcoma, while 3 (1.7%) were reported as suspicious.
  • [MeSH-major] Biopsy, Fine-Needle. Neoplasm Recurrence, Local / pathology. Rhabdomyosarcoma / pathology
  • [MeSH-minor] Adolescent. Adult. Carcinoma, Small Cell / pathology. Child. Child, Preschool. Diagnosis, Differential. Female. Humans. Infant. Infant, Newborn. Male. Retrospective Studies. Sarcoma / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Copyright] Copyright 2007 Wiley-Liss, Inc.
  • (PMID = 17636492.001).
  • [ISSN] 8755-1039
  • [Journal-full-title] Diagnostic cytopathology
  • [ISO-abbreviation] Diagn. Cytopathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


88. Fatusi OA, Ajike SO, Olateju SO, Adebayo AT, Gbolahan OO, Ogunmuyiwa SA: Clinico-epidemiological analysis of orofacial rhabdomyosarcoma in a Nigerian population. Int J Oral Maxillofac Surg; 2009 Mar;38(3):256-60
NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Clinico-epidemiological analysis of orofacial rhabdomyosarcoma in a Nigerian population.
  • Rhabdomyosarcoma (RMS) is a malignant soft tissue neoplasm, with varying degrees of striated muscle cell differentiation and a relative predilection for the head and neck region.
  • [MeSH-major] Facial Neoplasms / epidemiology. Head and Neck Neoplasms / epidemiology. Mouth Neoplasms / epidemiology. Neoplasms, Multiple Primary / epidemiology. Rhabdomyosarcoma / epidemiology
  • [MeSH-minor] Adolescent. Adult. Age Factors. Chi-Square Distribution. Child. Child, Preschool. Female. Humans. Infant. Infant, Newborn. Male. Nigeria / epidemiology. Statistics, Nonparametric. Young Adult

  • MedlinePlus Health Information. consumer health - Head and Neck Cancer.
  • MedlinePlus Health Information. consumer health - Oral Cancer.
  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19153030.001).
  • [ISSN] 1399-0020
  • [Journal-full-title] International journal of oral and maxillofacial surgery
  • [ISO-abbreviation] Int J Oral Maxillofac Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Denmark
  •  go-up   go-down


89. Bisogno G, Ferrari A, Prete A, Messina C, Basso E, Cecchetto G, Indolfi P, Scarzello G, D'Angelo P, De Sio L, Di Cataldo A, Carli M: Sequential high-dose chemotherapy for children with metastatic rhabdomyosarcoma. Eur J Cancer; 2009 Nov;45(17):3035-41
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Sequential high-dose chemotherapy for children with metastatic rhabdomyosarcoma.
  • AIM: The RMS4.99 study was designed to explore the role of multiple sequential high-dose chemotherapy cycles administered early in the treatment of children with metastatic rhabdomyosarcoma.
  • The use of sequential cycles of high-dose chemotherapy did not appear of benefit for patients with metastatic rhabdomyosarcoma.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Rhabdomyosarcoma / drug therapy. Rhabdomyosarcoma / secondary
  • [MeSH-minor] Adolescent. Age Factors. Child. Child, Preschool. Combined Modality Therapy. Disease Progression. Drug Administration Schedule. Epidemiologic Methods. Female. Humans. Infant. Male. Peripheral Blood Stem Cell Transplantation. Prognosis. Treatment Outcome. Young Adult

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19783136.001).
  • [ISSN] 1879-0852
  • [Journal-full-title] European journal of cancer (Oxford, England : 1990)
  • [ISO-abbreviation] Eur. J. Cancer
  • [Language] eng
  • [Publication-type] Clinical Trial; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  •  go-up   go-down


90. Kazanowska B, Reich A, Stegmaier S, Békássy AN, Leuschner I, Chybicka A, Koscielniak E: Pax3-fkhr and pax7-fkhr fusion genes impact outcome of alveolar rhabdomyosarcoma in children. Fetal Pediatr Pathol; 2007 Jan-Feb;26(1):17-31
NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Pax3-fkhr and pax7-fkhr fusion genes impact outcome of alveolar rhabdomyosarcoma in children.
  • Rhabdomyosarcoma is a highly malignant embryonic tumor of childhood.
  • [MeSH-major] Forkhead Transcription Factors / genetics. PAX7 Transcription Factor / genetics. Paired Box Transcription Factors / genetics. Rhabdomyosarcoma, Alveolar / diagnosis. Rhabdomyosarcoma, Alveolar / genetics
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Female. Gene Fusion. Head and Neck Neoplasms / diagnosis. Head and Neck Neoplasms / genetics. Head and Neck Neoplasms / pathology. Humans. Infant. Male. Neoplasm Staging. Prognosis. Retrospective Studies. Survival Analysis. Translocation, Genetic. Urinary Bladder Neoplasms / diagnosis. Urinary Bladder Neoplasms / genetics. Urinary Bladder Neoplasms / pathology. Urogenital Neoplasms / diagnosis. Urogenital Neoplasms / genetics. Urogenital Neoplasms / pathology

  • Genetic Alliance. consumer health - Rhabdomyosarcoma alveolar.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17613043.001).
  • [ISSN] 1551-3815
  • [Journal-full-title] Fetal and pediatric pathology
  • [ISO-abbreviation] Fetal Pediatr Pathol
  • [Language] eng
  • [Publication-type] Journal Article; Multicenter Study
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / FOXO1 protein, human; 0 / Forkhead Transcription Factors; 0 / PAX3 protein, human; 0 / PAX7 Transcription Factor; 0 / PAX7 protein, human; 0 / Paired Box Transcription Factors
  •  go-up   go-down


91. Ghaemmaghami F, Karimi Zarchi M, Ghasemi M: Lower genital tract rhabdomyosarcoma: case series and literature review. Arch Gynecol Obstet; 2008 Jul;278(1):65-9
International Agency for Research on Cancer - Screening Group. diagnostics - Histopathology and cytopathology of the uterine cervix - digital atlas .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Lower genital tract rhabdomyosarcoma: case series and literature review.
  • OBJECTIVE: Rhabdomyosarcoma (RMS) of the lower genital tract is a rare tumor.
  • [MeSH-major] Rhabdomyosarcoma / pathology. Rhabdomyosarcoma / therapy. Uterine Cervical Neoplasms / pathology. Uterine Cervical Neoplasms / therapy. Vaginal Neoplasms / pathology. Vaginal Neoplasms / therapy
  • [MeSH-minor] Adolescent. Adult. Chemotherapy, Adjuvant. Female. Humans. Neoplasm Recurrence, Local / therapy. Radiotherapy, Adjuvant. Registries. Uterine Hemorrhage / etiology

  • MedlinePlus Health Information. consumer health - Cervical Cancer.
  • MedlinePlus Health Information. consumer health - Vaginal Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18427824.001).
  • [ISSN] 0932-0067
  • [Journal-full-title] Archives of gynecology and obstetrics
  • [ISO-abbreviation] Arch. Gynecol. Obstet.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 15
  •  go-up   go-down


92. Ballard KS, Tedjarati SS, Robinson WR, Homesley HD, Thurston EL: Embryonal rhabdomyosarcoma: adjuvant and ex vivo assay-directed chemotherapy. Int J Gynecol Cancer; 2010 May;20(4):561-3
The Lens. Cited by Patents in .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Embryonal rhabdomyosarcoma: adjuvant and ex vivo assay-directed chemotherapy.
  • The aim of this retrospective study was to evaluate differences in treatment of embryonal rhabdomyosarcoma (RMS) of the uterus in 2 premenopausal women.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Rhabdomyosarcoma, Embryonal / drug therapy
  • [MeSH-minor] Adult. Chemotherapy, Adjuvant. Female. Humans. Remission Induction. Retrospective Studies. Survival Rate. Treatment Outcome. Young Adult

  • Genetic Alliance. consumer health - Rhabdomyosarcoma embryonal.
  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20442589.001).
  • [ISSN] 1525-1438
  • [Journal-full-title] International journal of gynecological cancer : official journal of the International Gynecological Cancer Society
  • [ISO-abbreviation] Int. J. Gynecol. Cancer
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


93. Douglas JG, Arndt CA, Hawkins DS: Delayed radiotherapy following dose intensive chemotherapy for parameningeal rhabdomyosarcoma (PM-RMS) of childhood. Eur J Cancer; 2007 Apr;43(6):1045-50
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Delayed radiotherapy following dose intensive chemotherapy for parameningeal rhabdomyosarcoma (PM-RMS) of childhood.
  • PURPOSE: To evaluate the local control rates and survival rates of patients with Group III parameningeal rhabdomyosarcoma (PM-RMS) treated with a dose intensive chemotherapy regimen followed by irradiation.
  • [MeSH-major] Meningeal Neoplasms / drug therapy. Meningeal Neoplasms / radiotherapy. Rhabdomyosarcoma, Alveolar / drug therapy. Rhabdomyosarcoma, Alveolar / radiotherapy. Rhabdomyosarcoma, Embryonal / drug therapy. Rhabdomyosarcoma, Embryonal / radiotherapy
  • [MeSH-minor] Adolescent. Adult. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Child. Child, Preschool. Combined Modality Therapy / methods. Disease-Free Survival. Female. Humans. Infant. Male. Pilot Projects. Prospective Studies. Time Factors. Tomography, X-Ray Computed. Treatment Outcome

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17368885.001).
  • [ISSN] 0959-8049
  • [Journal-full-title] European journal of cancer (Oxford, England : 1990)
  • [ISO-abbreviation] Eur. J. Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Multicenter Study
  • [Publication-country] England
  •  go-up   go-down


94. Haroun SA, Elnaiem EA, Zaki ZM, Adam I: Aggressive rhabdomyosarcoma of the vulva in a young Sudanese woman. Saudi Med J; 2007 Mar;28(3):461-2
MedlinePlus Health Information. consumer health - Vulvar Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Aggressive rhabdomyosarcoma of the vulva in a young Sudanese woman.
  • Pathological evaluation revealed pleomorphic rhabdomyosarcoma.
  • [MeSH-major] Neoplasm Invasiveness / pathology. Rhabdomyosarcoma / pathology. Vulvar Neoplasms / pathology
  • [MeSH-minor] Adult. Biopsy, Needle. Disease Progression. Fatal Outcome. Female. Humans. Immunohistochemistry. Neoplasm Staging. Sudan. Terminally Ill

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17334481.001).
  • [ISSN] 0379-5284
  • [Journal-full-title] Saudi medical journal
  • [ISO-abbreviation] Saudi Med J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Saudi Arabia
  •  go-up   go-down


95. Krsková L, Mrhalová M, Hilská I, Sumerauer D, Drahokoupilová E, Múdry P, Kodet R: Detection and clinical significance of bone marrow involvement in patients with rhabdomyosarcoma. Virchows Arch; 2010 May;456(5):463-72
NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Detection and clinical significance of bone marrow involvement in patients with rhabdomyosarcoma.
  • Childhood rhabdomyosarcoma (RMS) has two major histological subtypes: alveolar (aRMS) and embryonal.
  • [MeSH-major] Biomarkers, Tumor / analysis. Bone Marrow / pathology. Forkhead Transcription Factors / analysis. PAX7 Transcription Factor / analysis. Rhabdomyosarcoma / pathology. Rhabdomyosarcoma, Alveolar / pathology
  • [MeSH-minor] Adolescent. Child. Child, Preschool. Female. Humans. Infant. Male. MyoD Protein / genetics. Neoplasm Recurrence, Local / pathology. Paired Box Transcription Factors / analysis. Prognosis. Recombinant Fusion Proteins / analysis. Reverse Transcriptase Polymerase Chain Reaction / methods. Rhabdomyosarcoma, Embryonal / genetics. Rhabdomyosarcoma, Embryonal / pathology. Young Adult

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20405298.001).
  • [ISSN] 1432-2307
  • [Journal-full-title] Virchows Archiv : an international journal of pathology
  • [ISO-abbreviation] Virchows Arch.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / FOXO1 protein, human; 0 / Forkhead Transcription Factors; 0 / MyoD Protein; 0 / MyoD1 myogenic differentiation protein; 0 / PAX3 protein, human; 0 / PAX7 Transcription Factor; 0 / PAX7 protein, human; 0 / Paired Box Transcription Factors; 0 / Recombinant Fusion Proteins
  •  go-up   go-down


96. Carey KA, Segal D, Klein R, Sanigorski A, Walder K, Collier GR, Cameron-Smith D: Identification of novel genes expressed during rhabdomyosarcoma differentiation using cDNA microarrays. Pathol Int; 2006 May;56(5):246-55
NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Identification of novel genes expressed during rhabdomyosarcoma differentiation using cDNA microarrays.
  • These results identify several new genes with potential roles in the myogenic arrest present in rhabdomyosarcoma.
  • [MeSH-major] Cell Transformation, Neoplastic / genetics. Gene Expression Profiling. Oligonucleotide Array Sequence Analysis / methods. Rhabdomyosarcoma / genetics. Soft Tissue Neoplasms / genetics
  • [MeSH-minor] Adult. Cell Line, Tumor / drug effects. Cell Line, Tumor / metabolism. Cell Line, Tumor / pathology. Female. Gene Expression Regulation, Neoplastic. Humans. Male. Membrane Proteins / genetics. Membrane Proteins / metabolism. Muscle, Skeletal / cytology. Protein Precursors / genetics. Protein Precursors / metabolism. RNA, Messenger / metabolism. RNA, Neoplasm / analysis. Reverse Transcriptase Polymerase Chain Reaction. Saccharomyces cerevisiae Proteins / genetics. Saccharomyces cerevisiae Proteins / metabolism. Tetradecanoylphorbol Acetate / pharmacology. Thymosin / analogs & derivatives. Thymosin / genetics. Thymosin / metabolism

  • COS Scholar Universe. author profiles.
  • Hazardous Substances Data Bank. 12-O-TETRADECANOYLPHORBOL-13-ACETATE .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16669873.001).
  • [ISSN] 1320-5463
  • [Journal-full-title] Pathology international
  • [ISO-abbreviation] Pathol. Int.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Australia
  • [Chemical-registry-number] 0 / Membrane Proteins; 0 / Protein Precursors; 0 / RNA, Messenger; 0 / RNA, Neoplasm; 0 / Saccharomyces cerevisiae Proteins; 0 / TIM10 protein, S cerevisiae; 0 / prothymosin alpha; 61512-21-8 / Thymosin; NI40JAQ945 / Tetradecanoylphorbol Acetate
  •  go-up   go-down


97. Wolden SL: Radiation therapy for non-rhabdomyosarcoma soft tissue sarcomas in adolescents and young adults. J Pediatr Hematol Oncol; 2005 Apr;27(4):212-4
MedlinePlus Health Information. consumer health - Soft Tissue Sarcoma.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Radiation therapy for non-rhabdomyosarcoma soft tissue sarcomas in adolescents and young adults.
  • Non-rhabdomyosarcoma soft tissue sarcomas (NRSTS) are less responsive to radiotherapy than the more common pediatric soft tissue sarcomas, rhabdomyosarcoma and Ewing sarcoma of soft tissue.
  • However, radiation therapy does play an important role in the treatment of NRSTS, including synovial sarcoma.
  • [MeSH-major] Brachytherapy. Rhabdomyosarcoma / radiotherapy. Sarcoma / radiotherapy
  • [MeSH-minor] Adolescent. Adult. Humans. Practice Guidelines as Topic. Radiotherapy Dosage. Radiotherapy, Adjuvant

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15838393.001).
  • [ISSN] 1077-4114
  • [Journal-full-title] Journal of pediatric hematology/oncology
  • [ISO-abbreviation] J. Pediatr. Hematol. Oncol.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 11
  •  go-up   go-down


98. Houreih MA, Lin AY, Eyden B, Menasce LP, Harrison J, Jones D, Folberg R, Chejfec G, Banerjee SS: Alveolar rhabdomyosarcoma with neuroendocrine/neuronal differentiation: report of 3 cases. Int J Surg Pathol; 2009 Apr;17(2):135-41
NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Alveolar rhabdomyosarcoma with neuroendocrine/neuronal differentiation: report of 3 cases.
  • The aim of this study is to report the clinicopathologic characteristics of 3 cases of alveolar rhabdomyosarcoma with neuroendocrine/neuronal differentiation.
  • Specimens of 3 cases of alveolar rhabdomyosarcoma were studied using histologic, immunohistochemical, ultrastructural, and molecular genetic techniques.
  • The patients were a 19-year-old man with metastatic alveolar rhabdomyosarcoma in a groin lymph node, a 16-year-old girl with alveolar rhabdomyosarcoma of the perineum, and a 20-year-old man with recurrent orbital alveolar rhabdomyosarcoma.
  • The data presented expands the known differentiation of alveolar rhabdomyosarcoma.
  • [MeSH-major] Cell Differentiation. Genital Neoplasms, Female / pathology. Lymphoma / pathology. Neuroendocrine Cells / pathology. Neurons / pathology. Orbital Neoplasms / pathology. Rhabdomyosarcoma, Alveolar / pathology
  • [MeSH-minor] Adolescent. Biomarkers, Tumor / metabolism. Chromogranins / metabolism. Desmin / metabolism. Female. Humans. Male. Myogenin / metabolism. Synaptophysin / metabolism. Young Adult

  • Genetic Alliance. consumer health - Rhabdomyosarcoma alveolar.
  • MedlinePlus Health Information. consumer health - Lymphoma.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18611935.001).
  • [ISSN] 1066-8969
  • [Journal-full-title] International journal of surgical pathology
  • [ISO-abbreviation] Int. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Chromogranins; 0 / Desmin; 0 / Myogenin; 0 / Synaptophysin
  •  go-up   go-down


99. Bortoluzzi S, Bisognin A, Romualdi C, Danieli GA: Novel genes, possibly relevant for molecular diagnosis or therapy of human rhabdomyosarcoma, detected by genomic expression profiling. Gene; 2005 Mar 28;348:65-71
COS Scholar Universe. author profiles.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Novel genes, possibly relevant for molecular diagnosis or therapy of human rhabdomyosarcoma, detected by genomic expression profiling.
  • Transcriptional profiles of an alveolar rhabdomyosarcoma (RMS) and of a RMS cell line were reconstructed by a computational and statistical approach.
  • Expression data of 29,963 genes in 11 adult human healthy tissues and in 37 tumour tissues were analysed for comparison.
  • Cluster analysis applied to expression data detected a series of genes presumably co-expressed with genes encoding known tumour markers and/or reportedly involved in genesis or development of rhabdomyosarcoma.
  • [MeSH-major] Gene Expression Profiling. Oncogenes / genetics. Rhabdomyosarcoma / genetics
  • [MeSH-minor] Adult. Cluster Analysis. Female. Gene Expression Regulation, Neoplastic. Gene Library. Humans. Male. Neoplasms / genetics

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15777710.001).
  • [ISSN] 0378-1119
  • [Journal-full-title] Gene
  • [ISO-abbreviation] Gene
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Netherlands
  •  go-up   go-down


100. Ognjanovic S, Linabery AM, Charbonneau B, Ross JA: Trends in childhood rhabdomyosarcoma incidence and survival in the United States, 1975-2005. Cancer; 2009 Sep 15;115(18):4218-26
The Lens. Cited by Patents in .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Trends in childhood rhabdomyosarcoma incidence and survival in the United States, 1975-2005.
  • BACKGROUND: Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma in children and adolescents aged<20 years; its etiology remains largely unknown.
  • It is believed that embryonal (ERMS) and alveolar rhabdomyosarcoma (ARMS), the most common subtypes, arise through distinct biologic mechanisms.

  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Copyright] Copyright (c) 2009 American Cancer Society.
  • [Cites] Pediatr Dev Pathol. 2001 Nov-Dec;4(6):550-8 [11826361.001]
  • [Cites] Oncogene. 2001 Sep 10;20(40):5736-46 [11607823.001]
  • [Cites] Biometrics. 1983 Dec;39(4):941-8 [6671129.001]
  • [Cites] Med Pediatr Oncol. 1988;16(1):33-9 [3277029.001]
  • [Cites] Br J Cancer. 1988 Dec;58(6):838-42 [3224086.001]
  • [Cites] Science. 1990 Nov 30;250(4985):1233-8 [1978757.001]
  • [Cites] Int J Cancer. 1992 Feb 1;50(3):365-8 [1735603.001]
  • [Cites] Cancer Causes Control. 1993 May;4(3):217-24 [8318638.001]
  • [Cites] Genet Epidemiol. 1995;12(5):467-74 [8557179.001]
  • [Cites] Cancer. 1995 Sep 15;76(6):1073-85 [8625211.001]
  • [Cites] Cancer. 1995 Dec 1;76(11):2343-50 [8635041.001]
  • [Cites] Cancer. 1996 Oct 1;78(7):1483-91 [8839555.001]
  • [Cites] Diagn Mol Pathol. 1997 Apr;6(2):91-7 [9098647.001]
  • [Cites] Cancer Res. 1999 Apr 1;59(7 Suppl):1743s-1746s [10197590.001]
  • [Cites] Oncologist. 1999;4(1):34-44 [10337369.001]
  • [Cites] Pediatr Dev Pathol. 1998 Nov-Dec;1(6):550-61 [9724344.001]
  • [Cites] Cancer. 2005 Apr 1;103(7):1457-67 [15712273.001]
  • [Cites] Cancer Res. 2006 Jul 15;66(14):6936-46 [16849537.001]
  • [Cites] J Pathol. 2007 Jun;212(2):143-51 [17471488.001]
  • [Cites] Med Sci Monit. 2008 Jan;14(1):RA8-15 [18160950.001]
  • [Cites] Cancer. 2008 Jan 15;112(2):416-32 [18074355.001]
  • [Cites] Bone. 2008 May;42(5):982-9 [18337201.001]
  • [Cites] Am J Med Genet C Semin Med Genet. 2003 Feb 15;117C(1):42-8 [12561057.001]
  • [Cites] Cancer Res. 2003 Oct 15;63(20):6643-50 [14583457.001]
  • [Cites] J Pediatr. 2004 May;144(5):666-8 [15127010.001]
  • [Cites] Curr Probl Cancer. 1978 Mar;2(9):1-36 [109248.001]
  • [Cites] Eur J Cancer. 2008 Oct;44(15):2226-32 [18691878.001]
  • [Cites] Med Pediatr Oncol. 2002 Dec;39(6):554-7; discussion 552-3 [12376977.001]
  • [Cites] J Natl Cancer Inst. 1982 Jan;68(1):107-13 [6948120.001]
  • (PMID = 19536876.001).
  • [ISSN] 0008-543X
  • [Journal-full-title] Cancer
  • [ISO-abbreviation] Cancer
  • [Language] ENG
  • [Grant] United States / NCI NIH HHS / CA / T32 CA099936-07; United States / NCI NIH HHS / CA / T32 CA099936-06S1; United States / NCI NIH HHS / CA / CA099936-07; United States / NCI NIH HHS / CA / T32 CA099936; United States / NCI NIH HHS / CA / CA099936-06S1
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Other-IDs] NLM/ NIHMS218300; NLM/ PMC2953716
  •  go-up   go-down






Advertisement