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1. Ruijs MW, Verhoef S, Rookus MA, Pruntel R, van der Hout AH, Hogervorst FB, Kluijt I, Sijmons RH, Aalfs CM, Wagner A, Ausems MG, Hoogerbrugge N, van Asperen CJ, Gomez Garcia EB, Meijers-Heijboer H, Ten Kate LP, Menko FH, van 't Veer LJ: TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes. J Med Genet; 2010 Jun;47(6):421-8
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  • The two mutations detected outside the 'Chompret group' were found in a child with rhabdomyosarcoma and a young woman with breast cancer.
  • In addition, TP53 mutation testing can be considered in the event of childhood sarcoma and breast cancer before 30 years.
  • [MeSH-minor] Adult. Colonic Neoplasms / diagnosis. Colonic Neoplasms / genetics. DNA Mutational Analysis. Family Health. Female. Gene Frequency. Genetic Predisposition to Disease. Genetic Testing / methods. Genotype. Humans. Male. Middle Aged. Netherlands. Pancreatic Neoplasms / diagnosis. Pancreatic Neoplasms / genetics. Phenotype. Risk Factors. Young Adult


2. 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
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  • [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

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  • (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
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3. Burke M, Anderson JR, Kao SC, Rodeberg D, Qualman SJ, Wolden SL, Meyer WH, Breitfeld PP, Soft Tissue Sarcoma Committee of the Children's Oncology Group: Assessment of response to induction therapy and its influence on 5-year failure-free survival in group III rhabdomyosarcoma: the Intergroup Rhabdomyosarcoma Study-IV experience--a report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group. J Clin Oncol; 2007 Nov 1;25(31):4909-13
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  • [Title] Assessment of response to induction therapy and its influence on 5-year failure-free survival in group III rhabdomyosarcoma: the Intergroup Rhabdomyosarcoma Study-IV experience--a report from the Soft Tissue Sarcoma Committee of the Children's Oncology Group.
  • PURPOSE: Initial response to induction chemotherapy predicts failure-free survival (FFS) in osteosarcoma and Ewing's sarcoma.
  • For Intergroup Rhabdomyosarcoma Study (IRS) IV patients with group III rhabdomyosarcoma, we assessed whether reported response assessed by anatomic imaging at week 8 predicted FFS.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / administration & dosage. Neoadjuvant Therapy. Rhabdomyosarcoma / drug therapy. Soft Tissue Neoplasms / drug therapy
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Dose Fractionation. Female. Humans. Infant. Male. Survival Analysis

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  • (PMID = 17971587.001).
  • [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
  • [Grant] United States / NCI NIH HHS / CA / CA 98543; United States / NCI NIH HHS / CA / U10 CA098413; United States / NCI NIH HHS / CA / U10 CA24507
  • [Publication-type] Journal Article; Randomized Controlled Trial; Research Support, N.I.H., Extramural
  • [Publication-country] United States
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4. Yeasmin S, Nakayama K, Oride A, Ishibashi M, Ishikawa N, Katagiri A, Iida K, Nakayama N, Miyazaki K: A case of extremely chemoresistant pure pleomorphic rhabdomyosarcoma of the uterus associated with a high serum LDH level. Eur J Gynaecol Oncol; 2008;29(5):518-22
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  • [Title] A case of extremely chemoresistant pure pleomorphic rhabdomyosarcoma of the uterus associated with a high serum LDH level.
  • BACKGROUND: Pleomorphic rhabdomyosarcoma (RMS) of gynecologic origin is an exceedingly rare, highly malignant tumor.
  • CONCLUSION: It is important to have better insight and to set a standard multimodal treatment for adult RMS.
  • [MeSH-major] L-Lactate Dehydrogenase / blood. Rhabdomyosarcoma / pathology. Uterine Neoplasms / pathology

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  • (PMID = 19051826.001).
  • [ISSN] 0392-2936
  • [Journal-full-title] European journal of gynaecological oncology
  • [ISO-abbreviation] Eur. J. Gynaecol. Oncol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Italy
  • [Chemical-registry-number] EC 1.1.1.27 / L-Lactate Dehydrogenase
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5. Suzuki S, Utsugisawa K, Nagane Y, Satoh T, Terayama Y, Suzuki N, Kuwana M: Classification of myasthenia gravis based on autoantibody status. Arch Neurol; 2007 Aug;64(8):1121-4
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  • MAIN OUTCOME MEASURES: Anti-Kv1.4 antibody was measured by an immunoprecipitation assay with sulfur 35-labeled extract from rhabdomyosarcoma cells.
  • [MeSH-minor] Adult. Age Factors. Aged. Cohort Studies. Connectin. Female. Humans. Immunoprecipitation. Kv1.4 Potassium Channel / immunology. Male. Middle Aged. Muscle Proteins / immunology. Myocarditis / complications. Myositis / complications. Protein Kinases / immunology. Receptors, Cholinergic / immunology. Retrospective Studies. Severity of Illness Index. Thymoma / complications. Thymus Neoplasms / complications

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  • (PMID = 17698702.001).
  • [ISSN] 0003-9942
  • [Journal-full-title] Archives of neurology
  • [ISO-abbreviation] Arch. Neurol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Autoantibodies; 0 / Connectin; 0 / Kv1.4 Potassium Channel; 0 / Muscle Proteins; 0 / Receptors, Cholinergic; 0 / TTN protein, human; EC 2.7.- / Protein Kinases
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6. Strege RJ, Kovács G, Meyer JE, Holland D, Claviez A, Mehdorn MH, Interdisciplinary Group of Orbitazentrum UK S-H: Perioperative intensity-modulated brachytherapy for refractory orbital rhabdomyosarcomas in children. Strahlenther Onkol; 2009 Dec;185(12):789-98
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  • All children were in Intergroup Rhabdomyosarcoma Study Group (IRSG) group III and had embryonal subtype.
  • [MeSH-major] Brachytherapy / methods. Neoplasm Recurrence, Local / radiotherapy. Orbital Neoplasms / radiotherapy. Orbital Neoplasms / surgery. Radiotherapy, Intensity-Modulated / methods. Rhabdomyosarcoma, Embryonal / radiotherapy. Rhabdomyosarcoma, Embryonal / surgery
  • [MeSH-minor] Adolescent. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Chemotherapy, Adjuvant. Child. Child, Preschool. Combined Modality Therapy. Female. Follow-Up Studies. Humans. Infant. Male. Orbit / radiation effects. Orbit / surgery. Patient Care Team. Prospective Studies. Radiation Injuries / etiology. Radiotherapy Planning, Computer-Assisted / methods. Young Adult

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  • (PMID = 20013088.001).
  • [ISSN] 1439-099X
  • [Journal-full-title] Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al]
  • [ISO-abbreviation] Strahlenther Onkol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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7. Yang XH, Wu QL, Yu XB, Xu CX, Ma BF, Zhang XM, Li SN, Lahn BT, Xiang AP: Nestin expression in different tumours and its relevance to malignant grade. J Clin Pathol; 2008 Apr;61(4):467-73
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  • Recently, nestin was detected in some neoplasms such as glioma, ependymoma, melanoma, rhabdomyosarcoma, gastrointestinal stromal tumour (GIST), and testicular stromal tumour.
  • [MeSH-minor] Adenocarcinoma / metabolism. Adenocarcinoma / pathology. Adult. Aged. Female. Gastrointestinal Stromal Tumors / metabolism. Gastrointestinal Stromal Tumors / pathology. Hemangiosarcoma / metabolism. Hemangiosarcoma / pathology. Humans. Immunoenzyme Techniques. Male. Middle Aged. Nestin. Pancreatic Neoplasms / metabolism. Pancreatic Neoplasms / pathology

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  • (PMID = 17873113.001).
  • [ISSN] 1472-4146
  • [Journal-full-title] Journal of clinical pathology
  • [ISO-abbreviation] J. Clin. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Intermediate Filament Proteins; 0 / NES protein, human; 0 / Neoplasm Proteins; 0 / Nerve Tissue Proteins; 0 / Nestin
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8. Magnanti BL, Dorak MT, Parker L, Craft AW, James PW, McNally RJ: Sex-specific incidence and temporal trends in solid tumours in young people from Northern England, 1968-2005. BMC Cancer; 2008;8:89
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  • For 0-14 year olds there were male-specific increases in the incidence of rhabdomyosarcoma (2.4% per annum; 95% CI: 0.2%-4.5%) and non-melanotic skin cancer (9.6%; 95% CI: 0.0%-19.2%) and female-specific increases for sympathetic nervous system tumours (2.2%; 95% CI: 0.4%-3.9%), gonadal germ cell tumours (8.6%; 95% CI: 4.3%-12.9%) and non-gonadal germ cell tumours (5.4%; 95% CI: 2.8%-7.9%).
  • [MeSH-minor] Adolescent. Adult. Age Factors. Child. Child, Preschool. England / epidemiology. Female. Humans. Incidence. Infant. Infant, Newborn. Male. Sex Factors. Time Factors

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  • (PMID = 18387183.001).
  • [ISSN] 1471-2407
  • [Journal-full-title] BMC cancer
  • [ISO-abbreviation] BMC Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2358914
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9. Petrov SV, Machado I, Boulytcheva IV, Noguera R, Pellin A, Bacchini P, Bertoni F, Llombart-Bosch A: New approaches in the diagnosis of small-cell round tumors of bone and soft tissue. Arkh Patol; 2009 Jan-Feb;71(1):34-40
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  • The diagnosis of 17 small-cell round tumors of the bone and soft tissue, which were histologically similar to Ewing's sarcoma (EWS), was verified on paraffin sections, by using tissue microarray (TMA) technology, immunohistochemistry, cytogenetic (FISH) and molecular biological (RT-PCR) methods.
  • Two patients were diagnosed as having primitive neuroectodermal tumor (PNET), synovial sarcoma was present in 1 patient, embryonic rhabdomyosarcoma in 1, high-grade undifferentiated sarcoma in 1 and diffuse B-cell large-cell lymphoma in 1.
  • [MeSH-minor] Adolescent. Adult. Aged. Child. Child, Preschool. Female. Humans. Infant. Male. Microarray Analysis / methods. Middle Aged. Reverse Transcriptase Polymerase Chain Reaction / methods. Sarcoma, Ewing / diagnosis. Sarcoma, Ewing / metabolism. Sarcoma, Ewing / pathology

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  • (PMID = 19514357.001).
  • [ISSN] 0004-1955
  • [Journal-full-title] Arkhiv patologii
  • [ISO-abbreviation] Arkh. Patol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Russia (Federation)
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10. Haga K, Kashiwagi A, Nagamori S, Yamashiro K: Adult paratesticular rhabdomyosarcoma. Nat Clin Pract Urol; 2005 Aug;2(8):398-402; quiz 403
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  • [Title] Adult paratesticular rhabdomyosarcoma.
  • DIAGNOSIS: Paratesticular rhabdomyosarcoma with lymph node metastasis.
  • [MeSH-major] Rhabdomyosarcoma. Testicular Neoplasms
  • [MeSH-minor] Adult. Humans. Male

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  • (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
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11. Seleye-Fubara D, Nwosu SO, Yellowe BE: Soft tissue sarcomas in the Niger Delta Region of Nigeria (a referral hospital's study). Niger J Med; 2005 Apr-Jun;14(2):188-94
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  • Rhabdomyosarcoma was most frequent (39.4%) while the least was leiomyosarcoma (1.5%).
  • [MeSH-major] Sarcoma / diagnosis. Soft Tissue Neoplasms / diagnosis
  • [MeSH-minor] Adolescent. Adult. Aged. Child. Child, Preschool. Female. Hospitals, Teaching. Humans. Male. Middle Aged. Nigeria / epidemiology. Referral and Consultation. Retrospective Studies. Sex Distribution

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  • [ErratumIn] Niger J Med. 2005 Oct-Dec;14(4):461. Bob-Yellowe, E [corrected to Yellowe, BE]
  • (PMID = 16083244.001).
  • [ISSN] 1115-2613
  • [Journal-full-title] Nigerian journal of medicine : journal of the National Association of Resident Doctors of Nigeria
  • [ISO-abbreviation] Niger J Med
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Nigeria
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12. Goldstein M, Meller I, Issakov J, Orr-Urtreger A: Novel genes implicated in embryonal, alveolar, and pleomorphic rhabdomyosarcoma: a cytogenetic and molecular analysis of primary tumors. Neoplasia; 2006 May;8(5):332-43
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  • [Title] Novel genes implicated in embryonal, alveolar, and pleomorphic rhabdomyosarcoma: a cytogenetic and molecular analysis of primary tumors.
  • Rhabdomyosarcoma, the most common pediatric soft tissue sarcoma, likely results from deregulation of the skeletal myogenesis program.
  • Using a combined approach of spectral karyotyping, array-based comparative genomic hybridization (CGH), and expression analysis, we examined 10 primary RMS tumors, including embryonal, alveolar, and the rare adult pleomorphic variant, to explore the involvement of different genes and genetic pathways in RMS tumorigenesis.
  • [MeSH-major] Biomarkers, Tumor / metabolism. Genetic Predisposition to Disease. Neoplasms / genetics. Rhabdomyosarcoma, Alveolar / genetics. Rhabdomyosarcoma, Alveolar / metabolism. Rhabdomyosarcoma, Embryonal / embryology. Rhabdomyosarcoma, Embryonal / genetics
  • [MeSH-minor] Adolescent. Adult. Aged. Cell Adhesion. Child. Child, Preschool. Cytoskeleton / metabolism. Female. Gene Expression Regulation, Neoplastic. Humans. Infant. Karyotyping. Lung Neoplasms / metabolism. Male. Nucleic Acid Hybridization


13. Dörr W, Köst S, Keinert K, Glaser FH, Endert G, Herrmann T: Early intestinal changes following abdominal radiotherapy comparison of endpoints. Strahlenther Onkol; 2006 Jan;182(1):1-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-minor] Abdomen / radiation effects. Adolescent. Adult. Aged. Dose Fractionation. Dose-Response Relationship, Radiation. Female. Hodgkin Disease / radiotherapy. Humans. Intestinal Absorption / radiation effects. Kidney Neoplasms / radiotherapy. Lymphoma, Non-Hodgkin / radiotherapy. Male. Middle Aged. Prospective Studies. Radiotherapy Dosage. Rhabdomyosarcoma / radiotherapy. Seminoma / radiotherapy. Stomach Neoplasms / radiotherapy. Testicular Neoplasms / radiotherapy. Time Factors. Vitamin B 12 / pharmacokinetics. Xylose / pharmacokinetics

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  • (PMID = 16404514.001).
  • [ISSN] 0179-7158
  • [Journal-full-title] Strahlentherapie und Onkologie : Organ der Deutschen Röntgengesellschaft ... [et al]
  • [ISO-abbreviation] Strahlenther Onkol
  • [Language] eng
  • [Publication-type] Comparative Study; Evaluation Studies; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] A1TA934AKO / Xylose; P6YC3EG204 / Vitamin B 12
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14. Young RH: Sex cord-stromal tumors of the ovary and testis: their similarities and differences with consideration of selected problems. Mod Pathol; 2005 Feb;18 Suppl 2:S81-98
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  • Heterologous tumors most often contain mucinous epithelium, sometimes with small foci of carcinoid or less commonly, and generally in poorly differentiated neoplasms, rhabdomyosarcoma or fetal-type cartilage.
  • Granulosa cell tumors are much more common in females and in both gonads are divided into adult and juvenile forms.

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  • (PMID = 15502809.001).
  • [ISSN] 0893-3952
  • [Journal-full-title] Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
  • [ISO-abbreviation] Mod. Pathol.
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 69
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15. O'Callaghan MG, House M, Ebay S, Bhadelia R: Rhabdomyoma of the head and neck demonstrated by prenatal magnetic resonance imaging. J Comput Assist Tomogr; 2005 Jan-Feb;29(1):130-2
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  • This benign tumor of skeletal muscle is uncommon and should not be confused with its malignant counterpart-rhabdomyosarcoma.
  • [MeSH-minor] Adult. Female. Follow-Up Studies. Gestational Age. Humans. Infant, Newborn. Neoplasm Recurrence, Local / pathology. Pregnancy. Ultrasonography, Prenatal


16. Punyko JA, Mertens AC, Gurney JG, Yasui Y, Donaldson SS, Rodeberg DA, Raney RB, Stovall M, Sklar CA, Robison LL, Baker KS: Long-term medical effects of childhood and adolescent rhabdomyosarcoma: a report from the childhood cancer survivor study. Pediatr Blood Cancer; 2005 Jun 15;44(7):643-53
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  • [Title] Long-term medical effects of childhood and adolescent rhabdomyosarcoma: a report from the childhood cancer survivor study.
  • BACKGROUND: This study was conducted to evaluate the incidence of adverse medical conditions and to assess the risk of developing these conditions in a cohort of long-term survivors of rhabdomyosarcoma (RMS) diagnosed before age 21.
  • [MeSH-major] Health Status. Rhabdomyosarcoma. Survivors
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Cohort Studies. Female. Health Surveys. Humans. Incidence. Infant. Male. Risk Factors. Siblings. Time Factors

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  • [Copyright] Copyright 2005 Wiley-Liss, Inc.
  • (PMID = 15700252.001).
  • [ISSN] 1545-5009
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / K23-CA85503; United States / NCI NIH HHS / CA / U24 CA55727
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S.
  • [Publication-country] United States
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17. 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
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  • [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

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  • (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
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18. Kalu E, Creighton SM, Woodhouse CR: Vaginal restoration in survivors of childhood rhabdomyosarcoma. Int J Gynecol Cancer; 2009 Jul;19(5):981-4
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  • [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

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  • (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
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19. Mandong BM, Kidmas AT, Manasseh AN, Echejoh GO, Tanko MN, Madaki AJ: Epidemiology of soft tissue sarcomas in Jos, North Central Nigeria. Niger J Med; 2007 Jul-Sep;16(3):246-9
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  • Kaposi sarcoma (KS), Rhabdomyosarcoma (RMS), Malignant Fibrous Histiocytoma (MFH), and Fibrosarcoma (FS) were the commonest histological subtypes accounting for 69 (25.9%), 63 (23.7%), 56 (21.1%) and 49 (18.4%) respectively; with Rhabdomyosarcoma occurring more in paediatric and adolescent age groups, while the rest subtypes were more prevalent in adults.
  • [MeSH-major] Sarcoma / epidemiology. Soft Tissue Neoplasms / epidemiology
  • [MeSH-minor] Adult. Age Distribution. Female. Histiocytoma. Humans. Male. Middle Aged. Nigeria / epidemiology. Prevalence. Retrospective Studies. Rhabdomyosarcoma

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  • (PMID = 17937163.001).
  • [ISSN] 1115-2613
  • [Journal-full-title] Nigerian journal of medicine : journal of the National Association of Resident Doctors of Nigeria
  • [ISO-abbreviation] Niger J Med
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Nigeria
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20. Brecht IB, Ferrari A, Int-Veen C, Schuck A, Mattke AC, Casanova M, Bisogno G, Carli M, Koscielniak E, Treuner J: Grossly-resected synovial sarcoma treated by the German and Italian Pediatric Soft Tissue Sarcoma Cooperative Groups: discussion on the role of adjuvant therapies. Pediatr Blood Cancer; 2006 Jan;46(1):11-7
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  • [Title] Grossly-resected synovial sarcoma treated by the German and Italian Pediatric Soft Tissue Sarcoma Cooperative Groups: discussion on the role of adjuvant therapies.
  • Differently from adult oncologists that considered synovial sarcoma (SS) a tumor with uncertain chemosensitiveness, since two decades pediatric oncologists in Europe assumed that chemotherapy played an important role in SS treatment, so most pediatric patients were included in rhabdomyosarcoma protocols, receiving adjuvant chemotherapy regardless of risk factors.
  • [MeSH-major] Chemotherapy, Adjuvant. Radiotherapy, Adjuvant. Sarcoma, Synovial / therapy. Soft Tissue Neoplasms / therapy
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Disease-Free Survival. Female. Germany / epidemiology. Humans. Infant. Italy / epidemiology. Male. Survival Rate

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  • (PMID = 16292743.001).
  • [ISSN] 1545-5009
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] United States
  • [Number-of-references] 31
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21. Ballas K, Kontoulis TM, Papavasiliou A, Pissas D, Pavlidis T, Katsiki E, Venizelos I, Sakadamis A: A rare case of malignant triton tumor with pluridirectional differentiation. South Med J; 2009 Apr;102(4):435-7
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  • [MeSH-major] Nerve Sheath Neoplasms / pathology. Rhabdomyosarcoma / pathology. Soft Tissue Neoplasms / pathology
  • [MeSH-minor] Adult. Biomarkers, Tumor / analysis. Chondrosarcoma / pathology. Diagnosis, Differential. Humans. Immunohistochemistry. Male. Osteosarcoma / pathology

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  • (PMID = 19279515.001).
  • [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
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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22. Büttner A, Seifert K, Cottin T, Sarli V, Tzagkaroulaki L, Scholz S, Giannis A: Synthesis and biological evaluation of SANT-2 and analogues as inhibitors of the hedgehog signaling pathway. Bioorg Med Chem; 2009 Jul 15;17(14):4943-54
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  • Hedgehog (Hh) signaling plays an important role in cell signaling of embryonic development and adult tissue homeostasis.
  • Disruption of the Hh signaling pathway leads to severe disorders in the development of vertebrates whereas aberrant activation of the Hh pathway has been associated with several malignancies including Gorlin syndrome (a disorder predisposing to basal cell carcinoma, medulloblastoma and rhabdomyosarcoma), prostate, pancreatic and breast cancers.

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  • (PMID = 19541490.001).
  • [ISSN] 1464-3391
  • [Journal-full-title] Bioorganic & medicinal chemistry
  • [ISO-abbreviation] Bioorg. Med. Chem.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Benzamides; 0 / Benzimidazoles; 0 / Gli protein; 0 / Hedgehog Proteins; 0 / Oncogene Proteins; 0 / SANT-2 compound; 0 / Trans-Activators
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23. Janet NL, May AW, Akins RS: Sarcoma of the prostate: a single institutional review. Am J Clin Oncol; 2009 Feb;32(1):27-9
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  • [Title] Sarcoma of the prostate: a single institutional review.
  • OBJECTIVE: We report the management and outcome of prostate sarcoma at 1 institution and analyze factors that may determine prognosis.
  • MATERIALS AND METHODS: The medical records of 10 patients with prostate sarcoma were reviewed to identify symptoms at presentation, diagnostic procedures, and staging methods.
  • RESULTS: Five patients had rhabdomyosarcoma (RMS) and five had other subtypes, including two with carcinosarcoma, two with high-grade sarcoma not-otherwise-specified, and one with leiyomyosarcoma.
  • Of the eight with local disease, two had neoadjuvant chemotherapy and surgery, one had surgery alone, one had surgery and postoperative radiation, one had radiation alone, and three had chemoradiation.Chemotherapy consisted of vincristine, adriamycin, and cyclophosphomide for rhabdomyosarcoma and of cisplatin, adriamycin, and ifosphamide for the other subtypes.
  • The median survival for the rhabdomyosarcoma subgroup and nonrhabdomyosarcoma subroup is 142 months and 24 months, respectively.
  • CONCLUSIONS: In terms of tumor-related factors, the histologic subtype of prostate sarcoma appears to have prognostic significance.
  • [MeSH-major] Carcinosarcoma / therapy. Leiomyosarcoma / therapy. Prostatic Neoplasms / therapy. Rhabdomyosarcoma / therapy
  • [MeSH-minor] Adolescent. Adult. Aged. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Child, Preschool. Combined Modality Therapy. Follow-Up Studies. Humans. Male. Medical Records. Middle Aged. Prognosis. Prostatectomy. Radiotherapy Dosage. Survival Rate. Treatment Outcome. Young Adult

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  • (PMID = 19194120.001).
  • [ISSN] 1537-453X
  • [Journal-full-title] American journal of clinical oncology
  • [ISO-abbreviation] Am. J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Clinical Trial; Journal Article
  • [Publication-country] United States
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24. Navid F, Santana VM, Billups CA, Merchant TE, Furman WL, Spunt SL, Cain AM, Rao BN, Hale GA, Pappo AS: Concomitant administration of vincristine, doxorubicin, cyclophosphamide, ifosfamide, and etoposide for high-risk sarcomas: the St. Jude Children's Research Hospital experience. Cancer; 2006 Apr 15;106(8):1846-56
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  • METHODS: In the prospective high-risk sarcoma (HIRISA) Phase II trial HIRISA1, pediatric patients with high-risk sarcomas received 3 cycles of intensive vincristine, ifosfamide, etoposide, cyclophosphamide, and doxorubicin (VACIE) before radiotherapy and/or surgery began at Week 9 with concurrent vincristine, cyclophosphamide, and doxorubicin (Week 9) and vincristine and ifosfamide (Week 12).
  • RESULTS: Eleven of 24 patients (median age, 14.9 years) had Ewing sarcoma family of tumors, 9 patients had rhabdomyosarcoma, and 4 patients had unresectable desmoplastic small round cell tumors.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Bone Neoplasms / drug therapy. Sarcoma / drug therapy
  • [MeSH-minor] Adolescent. Adult. Child. Combined Modality Therapy. Cyclophosphamide / administration & dosage. Cyclophosphamide / adverse effects. Doxorubicin / administration & dosage. Doxorubicin / adverse effects. Etoposide / administration & dosage. Etoposide / adverse effects. Female. Humans. Ifosfamide / administration & dosage. Ifosfamide / adverse effects. Infant. Male. Rhabdomyosarcoma / drug therapy. Sarcoma, Ewing / drug therapy. Vincristine / administration & dosage. Vincristine / adverse effects

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  • [Copyright] 2006 American Cancer Society
  • (PMID = 16541446.001).
  • [ISSN] 0008-543X
  • [Journal-full-title] Cancer
  • [ISO-abbreviation] Cancer
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / CA21765
  • [Publication-type] Clinical Trial, Phase II; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 5J49Q6B70F / Vincristine; 6PLQ3CP4P3 / Etoposide; 80168379AG / Doxorubicin; 8N3DW7272P / Cyclophosphamide; UM20QQM95Y / Ifosfamide
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25. Mansky P, Arai A, Stratton P, Bernstein D, Long L, Reynolds J, Chen D, Steinberg SM, Lavende N, Hoffman K, Nathan PC, Parks R, Augustine E, Chaudhry U, Derdak J, Wiener L, Gerber L, Mackall C: Treatment late effects in long-term survivors of pediatric sarcoma. Pediatr Blood Cancer; 2007 Feb;48(2):192-9
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  • [Title] Treatment late effects in long-term survivors of pediatric sarcoma.
  • PATIENTS AND METHODS: Thirty-two individuals treated for Ewing sarcoma family of tumors (ESFT), rhabdomyosarcoma (RMS), or non-rhabdomyosarcoma soft tissue sarcomas (NR-STS) with multi-modality therapy were enrolled on this cross-sectional study.
  • RESULTS: This cohort of sarcoma survivors shows expected locoregional limitations in function of the area affected by sarcoma, and impaired global musculoskeletal functioning as evidenced by limited endurance and limited overall activity levels.
  • CONCLUSION: Sarcoma survivors demonstrate diminished locoregional and global musculoskeletal functioning which likely limit occupational opportunities and socioeconomic health.
  • In addition, the combination of diminished cardiac reserve, limited activity levels, and lipid dysregulation in sarcoma survivors suggests that this population is at increased risk for cardiovascular disease, even many years following completion of sarcoma therapy.
  • Sarcoma survivors may benefit from life long follow-up for cardiovascular disease and from occupational counseling upon completion of therapy.
  • [MeSH-major] Sarcoma / physiopathology. Sarcoma / therapy. Survivors
  • [MeSH-minor] Adolescent. Adult. Age Factors. Body Fat Distribution. Combined Modality Therapy. Cross-Sectional Studies. Female. Heart / physiopathology. Humans. Infertility, Male / etiology. Lipids / blood. Male. Menopause, Premature. Middle Aged. Musculoskeletal System / physiopathology. Physical Endurance / physiology. Sarcoma, Ewing / physiopathology. Sarcoma, Ewing / therapy. Soft Tissue Neoplasms / physiopathology. Soft Tissue Neoplasms / therapy

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  • (PMID = 16642490.001).
  • [ISSN] 1545-5009
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Grant] United States / Intramural NIH HHS / /
  • [Publication-type] Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Lipids
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26. Seleye-Fubara D, Etebu EN: Juvenile rhabdomyosarcomas in Port Harcourt, Nigeria: A twelve year review. West Afr J Med; 2006 Jan-Mar;25(1):57-60
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  • BACKGROUND: Juvenile rhabdomyosarcoma (JRMS) though rare, is the most common soft tissue malignancy of childhood that exhibits bimodal age distribution pattern.
  • The most common histologic type is the embryonal rhabdomyosarcoma (71.5%).
  • Alveolar rhabdomyosarcoma accounted for (19%) and the sarcoma botryoides (9.5%).
  • If a tumor histologically shows as small round blue cells, rhabdomyosarcoma should be considered as a differential diagnosis.
  • [MeSH-major] Rhabdomyosarcoma / epidemiology
  • [MeSH-minor] Abdomen. Adolescent. Adult. Age Distribution. Child. Child, Preschool. Female. Head. Humans. Infant. Infant, Newborn. Lower Extremity. Male. Nigeria / epidemiology. Retrospective Studies. Rhabdomyosarcoma, Alveolar / epidemiology. Rhabdomyosarcoma, Alveolar / pathology. Rhabdomyosarcoma, Embryonal / epidemiology. Rhabdomyosarcoma, Embryonal / pathology. Sarcoma / epidemiology. Sarcoma / pathology. Sex Distribution. Upper Extremity

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  • (PMID = 16722360.001).
  • [ISSN] 0189-160X
  • [Journal-full-title] West African journal of medicine
  • [ISO-abbreviation] West Afr J Med
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Nigeria
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27. Mello de Queiroz F, Suarez-Kurtz G, Stühmer W, Pardo LA: Ether à go-go potassium channel expression in soft tissue sarcoma patients. Mol Cancer; 2006;5:42
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  • [Title] Ether à go-go potassium channel expression in soft tissue sarcoma patients.
  • BACKGROUND: The expression of the human Eag1 potassium channel (Kv10.1) is normally restricted to the adult brain, but it has been detected in both tumour cell lines and primary tumours.
  • Our purpose was to determine the frequency of expression of Eag1 in soft tissue sarcoma and its potential clinical implications.
  • Eag1 was expressed in 71% of all tumours, with frequencies ranging from 56% (liposarcoma) to 82% (rhabdomyosarcoma).
  • Four cell lines derived from relevant sarcoma histological types (fibrosarcoma and rhabdomyosarcoma) were tested for Eag1 expression by real-time RT-PCR.
  • In sarcoma cell lines, inhibition of Eag1 expression and/or function leads to reduced proliferation.
  • [MeSH-major] Ether-A-Go-Go Potassium Channels / metabolism. Sarcoma / metabolism
  • [MeSH-minor] Adolescent. Adult. Aged. Animals. Biomarkers, Tumor / metabolism. CHO Cells. Cell Line, Tumor. Cell Proliferation. Cricetinae. Female. Gene Expression. Gene Expression Regulation, Neoplastic. Humans. Liposarcoma / metabolism. Male. Middle Aged. RNA Interference. Rhabdomyosarcoma / metabolism. Soft Tissue Neoplasms / metabolism. Specimen Handling. Transfection

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  • (PMID = 17022811.001).
  • [ISSN] 1476-4598
  • [Journal-full-title] Molecular cancer
  • [ISO-abbreviation] Mol. Cancer
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Ether-A-Go-Go Potassium Channels; 0 / KCNH1 protein, human
  • [Other-IDs] NLM/ PMC1618397
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28. Blandford MC, Barr FG, Lynch JC, Randall RL, Qualman SJ, Keller C: Rhabdomyosarcomas utilize developmental, myogenic growth factors for disease advantage: a report from the Children's Oncology Group. Pediatr Blood Cancer; 2006 Mar;46(3):329-38
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Unresectable or metastatic disease represents the greatest obstacle to cure for children with rhabdomyosarcoma.
  • PROCEDURE: Using oligonucleotide gene expression analysis for a focused set of 60 genes, we analyzed the myogenic expression profiles of 89 rhabdomyosarcomas from the Intergroup Rhabdomyosarcoma Study-IV.
  • [MeSH-major] Autocrine Communication. Gene Expression Regulation, Neoplastic. Neoplasm Proteins / biosynthesis. Receptors, Platelet-Derived Growth Factor / biosynthesis. Rhabdomyosarcoma / metabolism. Somatomedins / biosynthesis
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Cohort Studies. Disease-Free Survival. Female. Humans. Infant. Male. RNA, Messenger / biosynthesis. Reverse Transcriptase Polymerase Chain Reaction. Transcription, Genetic

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  • (PMID = 16261596.001).
  • [ISSN] 1545-5009
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Neoplasm Proteins; 0 / RNA, Messenger; 0 / Somatomedins; EC 2.7.10.1 / Receptors, Platelet-Derived Growth Factor
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29. Mohammadi S, Kadivar M, Mohebbi S, Eftekhari TF: Metastasis of sino-nasal rhabdomyosarcoma to breast. Breast J; 2008 Nov-Dec;14(6):596-7
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  • [Title] Metastasis of sino-nasal rhabdomyosarcoma to breast.
  • [MeSH-major] Breast Neoplasms / pathology. Breast Neoplasms / secondary. Neoplasm Metastasis / pathology. Nose Neoplasms / pathology. Rhabdomyosarcoma / pathology
  • [MeSH-minor] Fatal Outcome. Female. Humans. Paranasal Sinuses / pathology. Young Adult

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  • (PMID = 19000047.001).
  • [ISSN] 1524-4741
  • [Journal-full-title] The breast journal
  • [ISO-abbreviation] Breast J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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30. 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
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  • [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


31. Edil BH, Cameron JL, Reddy S, Lum Y, Lipsett PA, Nathan H, Pawlik TM, Choti MA, Wolfgang CL, Schulick RD: Choledochal cyst disease in children and adults: a 30-year single-institution experience. J Am Coll Surg; 2008 May;206(5):1000-5; discussion 1005-8
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  • Four adults (three with cholangiocarcinoma and one with gall bladder cancer) and one child (with embryonal rhabdomyosarcoma) had malignancies associated with their CC at the time of excision.
  • [MeSH-minor] Adolescent. Adult. Child. Female. Humans. Male. Retrospective Studies

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  • (PMID = 18471743.001).
  • [ISSN] 1879-1190
  • [Journal-full-title] Journal of the American College of Surgeons
  • [ISO-abbreviation] J. Am. Coll. Surg.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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32. Coleman DV, Poznansky JJ: Review of cervical smears from 76 women with invasive cervical cancer: cytological findings and medicolegal implications. Cytopathology; 2006 Jun;17(3):127-36
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  • One women was found to have an embryonal rhabdomyosarcoma of the corpus uteri involving the cervix.
  • [MeSH-minor] Adult. Aged. False Negative Reactions. Female. Great Britain. Humans. Middle Aged


33. Wolden SL, Alektiar KM: Sarcomas across the age spectrum. Semin Radiat Oncol; 2010 Jan;20(1):45-51
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  • For example, advances at the molecular level in Ewing sarcoma, a disease that affects predominantly children, helped spearhead the uncovering of several signature translocations in adult sarcomas, such as synovial sarcoma and myxoid liposarcomas.
  • The success of chemotherapy in pediatric sarcomas continues to be a benchmark for adult sarcomas to emulate.
  • Conversely, the demonstration of the viability of limb-sparing surgery combined with adjuvant radiation in adult extremity sarcomas helped advance that treatment approach in pediatric sarcomas.
  • To illustrate some of these concepts and to enhance our understanding of sarcomas across the age spectrum, 4 types of sarcoma are discussed.
  • The first 2 are Ewing sarcoma and rhabdomyosarcoma seen mainly, but not exclusively, in children.
  • The other 2 are synovial sarcoma, which can be looked at as a bridge between pediatric and adult sarcomas as it affects mainly young adults, and liposarcoma that is almost exclusively an adult sarcoma.
  • [MeSH-major] Sarcoma / epidemiology. Sarcoma / therapy
  • [MeSH-minor] Adolescent. Adult. Age Distribution. Aged. Child. Child, Preschool. Combined Modality Therapy / methods. Female. Humans. Infant. Infant, Newborn. Liposarcoma / epidemiology. Liposarcoma / therapy. Male. Middle Aged. Rhabdomyosarcoma / epidemiology. Rhabdomyosarcoma / therapy. Sarcoma, Ewing / epidemiology. Sarcoma, Ewing / therapy. Sarcoma, Synovial / epidemiology. Sarcoma, Synovial / therapy. Young Adult

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  • (PMID = 19959030.001).
  • [ISSN] 1532-9461
  • [Journal-full-title] Seminars in radiation oncology
  • [ISO-abbreviation] Semin Radiat Oncol
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 41
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34. 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
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  • [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

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  • (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
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35. Jha P, Frölich AM, McCarville B, Navarro OM, Babyn P, Goldsby R, Daldrup-Link H: Unusual association of alveolar rhabdomyosarcoma with pancreatic metastasis: emerging role of PET-CT in tumor staging. Pediatr Radiol; 2010 Aug;40(8):1380-6
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  • [Title] Unusual association of alveolar rhabdomyosarcoma with pancreatic metastasis: emerging role of PET-CT in tumor staging.
  • [MeSH-major] Pancreatic Neoplasms / complications. Pancreatic Neoplasms / radiography. Positron-Emission Tomography. Rhabdomyosarcoma, Alveolar / complications. Rhabdomyosarcoma, Alveolar / radiography
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Female. Humans. Male. Neoplasm Staging / methods. Recurrence. Retrospective Studies. Tomography, X-Ray Computed

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  • (PMID = 20180103.001).
  • [ISSN] 1432-1998
  • [Journal-full-title] Pediatric radiology
  • [ISO-abbreviation] Pediatr Radiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
  • [Other-IDs] NLM/ PMC2895865
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36. Sueters M, Peek AM, Ball LM, Hogendoorn PC, Scherjon SA, de Keizer RJ, Schalij-Delfos NE: Prenatal detection of orbital rhabdomyosarcoma. Arch Ophthalmol; 2005 Feb;123(2):276-9
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  • [Title] Prenatal detection of orbital rhabdomyosarcoma.
  • [MeSH-major] Orbital Neoplasms / ultrasonography. Rhabdomyosarcoma, Embryonal / ultrasonography. Ultrasonography, Prenatal
  • [MeSH-minor] Adult. Fatal Outcome. Female. Humans. Magnetic Resonance Imaging. Pregnancy. Ultrasonography, Doppler

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  • (PMID = 15710835.001).
  • [ISSN] 0003-9950
  • [Journal-full-title] Archives of ophthalmology (Chicago, Ill. : 1960)
  • [ISO-abbreviation] Arch. Ophthalmol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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37. De Sio L, Milano GM, Castellano A, Jenkner A, Fidani P, Dominici C, Donfrancesco A: Temozolomide in resistant or relapsed pediatric solid tumors. Pediatr Blood Cancer; 2006 Jul;47(1):30-6
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  • Tumor types were: neuroblastoma (NB; n = 17), medulloblastoma (MB; 8), brain stem glioma (BSG; 8), extraosseous Ewing's sarcoma/peripheral neuroectodermal tumor (EOES; 4), Ewing's sarcoma (ES; 4), anaplastic astrocytoma (AA; 3), rhabdomyosarcoma (RMS; 2), ependymoma (EP; 2), cerebral primitive neuroectodermal tumor (cPNET; 2), hepatocarcinoma (HC; 1), and osteosarcoma (OS; 1).
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Disease-Free Survival. Dose-Response Relationship, Drug. Female. Humans. Male. Survival Analysis

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  • [Copyright] Copyright 2006 Wiley-Liss, Inc.
  • [ErratumIn] Pediatr Blood Cancer. 2006 Oct 15;47(5):647-8
  • (PMID = 16047361.001).
  • [ISSN] 1545-5009
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] eng
  • [Publication-type] Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antineoplastic Agents, Alkylating; 7GR28W0FJI / Dacarbazine; 85622-93-1 / temozolomide
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38. Katabathina VS, Vikram R, Nagar AM, Tamboli P, Menias CO, Prasad SR: Mesenchymal neoplasms of the kidney in adults: imaging spectrum with radiologic-pathologic correlation. Radiographics; 2010 Oct;30(6):1525-40
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Malignant renal tumors of mesenchymal origin include leiomyosarcoma, rhabdomyosarcoma, angiosarcoma, osteosarcoma, synovial sarcoma, fibrosarcoma, malignant fibrous histiocytoma, and solitary fibrous tumor.
  • [MeSH-minor] Adult. Biopsy. Diagnosis, Differential. Humans

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  • [Copyright] © RSNA, 2010.
  • (PMID = 21071373.001).
  • [ISSN] 1527-1323
  • [Journal-full-title] Radiographics : a review publication of the Radiological Society of North America, Inc
  • [ISO-abbreviation] Radiographics
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
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39. Zhang HT, Guo L, Su Q: [Clinicopathologic analysis of spindle cell rhabdomyosarcoma: report of 8 cases]. Zhonghua Zhong Liu Za Zhi; 2008 Feb;30(2):141-3
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  • [Title] [Clinicopathologic analysis of spindle cell rhabdomyosarcoma: report of 8 cases].
  • OBJECTIVE: To study the clinicopathological features of spindle cell rhabdomyosarcoma (SCRMS) in order to differentiate it from other myosarcomas.
  • CONCLUSION: Spindle cell rhabdomyosarcoma is a rare embryonal rhabdomyosarcoma which occurs in the childhood or adulthood with a poor prognosis, and is frequently presented as a painless mass most frequently involveing the head and neck or cervical area or para-testis site.
  • [MeSH-major] Rhabdomyosarcoma, Embryonal / pathology. Rhabdomyosarcoma, Embryonal / surgery. Soft Tissue Neoplasms / pathology. Soft Tissue Neoplasms / surgery
  • [MeSH-minor] Adolescent. Adult. Child. Combined Modality Therapy. Desmin / metabolism. Diagnosis, Differential. Female. Follow-Up Studies. Humans. Male. Middle Aged. MyoD Protein / metabolism. Myoglobin / metabolism. Neoplasm Recurrence, Local. Retrospective Studies. Young Adult

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  • (PMID = 18646700.001).
  • [ISSN] 0253-3766
  • [Journal-full-title] Zhonghua zhong liu za zhi [Chinese journal of oncology]
  • [ISO-abbreviation] Zhonghua Zhong Liu Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] 0 / Desmin; 0 / MyoD Protein; 0 / MyoD1 myogenic differentiation protein; 0 / Myoglobin
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40. Suzuki S, Satoh T, Yasuoka H, Hamaguchi Y, Tanaka K, Kawakami Y, Suzuki N, Kuwana M: Novel autoantibodies to a voltage-gated potassium channel Kv1.4 in a severe form of myasthenia gravis. J Neuroimmunol; 2005 Dec 30;170(1-2):141-9
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  • Sera from patients with myasthenia gravis (MG) were screened for autoantibodies to skeletal muscle-specific antigens by immunoprecipitation assay, using rhabdomyosarcoma and leukemia cell lines.
  • Eleven of 61 MG sera immunoprecipitated a rhabdomyosarcoma-specific 70-kDa protein, which was identified as the voltage-gated K+ channel 1.4 (Kv1.4).
  • [MeSH-minor] Adult. Autoantigens / blood. Female. Humans. Immunoprecipitation. Male. Middle Aged. Molecular Weight. Muscle, Skeletal / immunology. RNA, Messenger / metabolism. Severity of Illness Index. Thymus Gland / metabolism

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  • (PMID = 16182377.001).
  • [ISSN] 0165-5728
  • [Journal-full-title] Journal of neuroimmunology
  • [ISO-abbreviation] J. Neuroimmunol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Netherlands
  • [Chemical-registry-number] 0 / Autoantibodies; 0 / Autoantigens; 0 / Kv1.4 Potassium Channel; 0 / RNA, Messenger
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41. 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
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  • [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

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  • (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
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42. 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
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  • [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

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  • (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
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43. 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
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  • [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

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  • (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
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44. Hossain GA, Moinul Islam SM, Mahmood S, Khan N, Chakrabarty RK: Tc-99m DTPA scintigraphy in soft tissue tumor. Mymensingh Med J; 2005 Jul;14(2):185-8
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  • Two cases of rhabdomyosarcoma showed consistently positive.

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  • (PMID = 16056208.001).
  • [ISSN] 1022-4742
  • [Journal-full-title] Mymensingh medical journal : MMJ
  • [ISO-abbreviation] Mymensingh Med J
  • [Language] ENG
  • [Publication-type] Journal Article
  • [Publication-country] Bangladesh
  • [Chemical-registry-number] 0 / Radiopharmaceuticals; VW78417PU1 / Technetium Tc 99m Pentetate
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45. Zur KB, Putnam PE, Rutter MJ: Combined retrograde and anterograde hypopharyngeal puncture and dilatation in a child with complete hypopharyngeal stenosis. Int J Pediatr Otorhinolaryngol; 2007 Jan;71(1):153-7
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  • The management of complete hypopharyngeal stenosis is a complex task, and various methods of re-creating a lumen and maintaining its patency have been described in both the adult and pediatric literature.
  • We present our experience using a modification of the combined anterograde-retrograde endoscopic technique for managing a 15-year-old child who developed complete hypopharyngeal and upper esophageal obliteration following successful treatment of a parapharyngeal rhabdomyosarcoma.
  • [MeSH-minor] Administration, Topical. Adolescent. Alkylating Agents / therapeutic use. Anti-Inflammatory Agents / therapeutic use. Constriction, Pathologic / etiology. Constriction, Pathologic / therapy. Humans. Injections, Intralesional. Male. Mitomycin / therapeutic use. Rhabdomyosarcoma / complications. Triamcinolone Acetonide / therapeutic use

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  • (PMID = 17081625.001).
  • [ISSN] 0165-5876
  • [Journal-full-title] International journal of pediatric otorhinolaryngology
  • [ISO-abbreviation] Int. J. Pediatr. Otorhinolaryngol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Ireland
  • [Chemical-registry-number] 0 / Alkylating Agents; 0 / Anti-Inflammatory Agents; 50SG953SK6 / Mitomycin; F446C597KA / Triamcinolone Acetonide
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46. Nitsche M, Hermann RM, Christiansen H, Berger J, Pradier O: Rationale for individualized therapy in Sinonasal Teratocarcinosarcoma (SNTC): case report. Onkologie; 2005 Dec;28(12):653-6
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  • Histology showed an SNTC with major parts of small cell, poorly differentiated carcinoma and a small proportion of highly differentiated embryonal rhabdomyosarcoma.
  • [MeSH-minor] Adult. Cisplatin / therapeutic use. Combined Modality Therapy. Etoposide / therapeutic use. Fluorouracil / therapeutic use. General Surgery. Humans. Ifosfamide / therapeutic use. Male. Radiotherapy, Adjuvant. Treatment Outcome

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  • (PMID = 16330889.001).
  • [ISSN] 0378-584X
  • [Journal-full-title] Onkologie
  • [ISO-abbreviation] Onkologie
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Switzerland
  • [Chemical-registry-number] 6PLQ3CP4P3 / Etoposide; Q20Q21Q62J / Cisplatin; U3P01618RT / Fluorouracil; UM20QQM95Y / Ifosfamide
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47. Admiraal R, van der Paardt M, Kobes J, Kremer LC, Bisogno G, Merks JH: High-dose chemotherapy for children and young adults with stage IV rhabdomyosarcoma. Cochrane Database Syst Rev; 2010;(12):CD006669
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  • [Title] High-dose chemotherapy for children and young adults with stage IV rhabdomyosarcoma.
  • BACKGROUND: Rhabdomyosarcoma is the most common soft tissue sarcoma of childhood.
  • High-dose chemotherapy (HDC) seems to be an attractive option to treat minimal residual disease in metastatic rhabdomyosarcoma patients.
  • OBJECTIVES: The objective of the review was to assess the effectiveness of HDC with stem cell rescue (SRC) versus standard-dose chemotherapy in improving event-free survival (EFS) and overall survival (OS) of children and young adults with metastatic rhabdomyosarcoma.
  • SELECTION CRITERIA: Randomised controlled trials (RCT), prospective or historical controlled clinical trials (CCT), in which HDC with SCR was compared to conventional chemotherapy and prospective case series (non-controlled clinical trials) including at least 20 naive metastatic rhabdomyosarcoma patients DATA COLLECTION AND ANALYSIS: Two review authors independently performed the study selection, quality assessment and data extraction.
  • AUTHORS' CONCLUSIONS: Overall, the results of this review do not justify the use of HDC with SCR as a standard therapy for children with metastatic rhabdomyosarcoma.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / administration & dosage. Rhabdomyosarcoma / drug therapy. Soft Tissue Neoplasms / drug therapy
  • [MeSH-minor] Child. Controlled Clinical Trials as Topic. Disease-Free Survival. Humans. Neoplasm Staging. Stem Cell Transplantation / methods. Transplantation, Autologous. Young Adult

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  • (PMID = 21154373.001).
  • [ISSN] 1469-493X
  • [Journal-full-title] The Cochrane database of systematic reviews
  • [ISO-abbreviation] Cochrane Database Syst Rev
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] England
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48. Kido A, Amano I, Honoki K, Tanaka H, Morii T, Fujii H, Yoshitani K, Tanaka Y: Allogeneic and autologous stem cell transplantation in advanced small round cell sarcomas. J Orthop Sci; 2010 Sep;15(5):690-5
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  • [MeSH-major] Hematopoietic Stem Cell Transplantation. Rhabdomyosarcoma / therapy. Sarcoma, Ewing / therapy
  • [MeSH-minor] Adolescent. Adult. Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Cord Blood Stem Cell Transplantation. Female. Humans. Salvage Therapy. Spinal Neoplasms / drug therapy. Spinal Neoplasms / therapy. Transplantation, Homologous. Young Adult

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  • (PMID = 20953934.001).
  • [ISSN] 1436-2023
  • [Journal-full-title] Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association
  • [ISO-abbreviation] J Orthop Sci
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Japan
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49. Contreras AL, Punar M, Tamboli P, Tu SM, Pisters L, Moran C, Czerniak BA, Guo CC: Mediastinal germ cell tumors with an angiosarcomatous component: a report of 12 cases. Hum Pathol; 2010 Jun;41(6):832-7
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  • In addition, other non-germ cell components, including rhabdomyosarcoma (n = 3), leiomyosarcoma (n = 1), and poorly differentiated carcinoma (n = 1), were also present in the tumors.
  • [MeSH-minor] Adult. Carcinoma / mortality. Carcinoma / pathology. Humans. Leiomyosarcoma / mortality. Leiomyosarcoma / pathology. Male. Neoplasm Metastasis. Neoplasm Recurrence, Local. Rhabdomyosarcoma / mortality. Rhabdomyosarcoma / pathology. Survival Rate. Young Adult

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  • [Copyright] Copyright 2010 Elsevier Inc. All rights reserved.
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  • (PMID = 20153508.001).
  • [ISSN] 1532-8392
  • [Journal-full-title] Human pathology
  • [ISO-abbreviation] Hum. Pathol.
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / P50 CA091846
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ NIHMS614200; NLM/ PMC4163004
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50. Hulse N, Raja S, Kumar A, Paul AS: Rhabdomyosarcoma of the extremities in adults. Acta Orthop Belg; 2006 Apr;72(2):199-203
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  • [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

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  • (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
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51. 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
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  • [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

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  • (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
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52. Vitovskiĭ RM: [Efficacy of the surgical treatment for malignant heart tumors]. Klin Khir; 2005 Jan;(1):35-8
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  • Rhabdomyosarcoma was diagnosed in 9 patients, angiosarcoma--in 11, leyomyosarcoma--in 6, malignant mixoma--in 4, fibrosarcoma, chondrosarcoma and liposarcoma--each as a single observation.

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  • (PMID = 15786840.001).
  • [ISSN] 0023-2130
  • [Journal-full-title] Klinichna khirurhiia
  • [ISO-abbreviation] Klin Khir
  • [Language] RUS
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Ukraine
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53. Yamada H, Mishima K, Kawaguchi K, Horiuchi T, Nakaoka K, Iino M, Saito I, Hamada Y: A nodular buccal mass. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2010 Aug;110(2):140-4
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  • [MeSH-major] Cheek / pathology. Masseter Muscle / pathology. Muscle Neoplasms / pathology. Rhabdomyosarcoma, Alveolar / pathology
  • [MeSH-minor] Chemotherapy, Adjuvant. Diagnosis, Differential. Humans. Male. Radiotherapy, Adjuvant. Young Adult

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  • (PMID = 20659696.001).
  • [ISSN] 1528-395X
  • [Journal-full-title] Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics
  • [ISO-abbreviation] Oral Surg Oral Med Oral Pathol Oral Radiol Endod
  • [Language] eng
  • [Publication-type] Case Reports; Clinical Conference; Journal Article
  • [Publication-country] United States
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54. Védrine PO, Coffinet L, Temam S, Montagne K, Lapeyre M, Oberlin O, Orbach D, Simon C, Sommelet D: Mucoepidermoid carcinoma of salivary glands in the pediatric age group: 18 clinical cases, including 11 second malignant neoplasms. Head Neck; 2006 Sep;28(9):827-33
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  • Eleven patients had been previously treated by radiotherapy and/or chemotherapy for a first malignant tumor, specifically, lymphoid leukemia (n = 4), lymphoma (n = 3), brain tumor (n = 2), sarcoma (n = 1), and retinoblastoma (n = 1).
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Female. Humans. Lymphoma / pathology. Male. Neoplasms, Neuroepithelial / pathology. Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology. Rhabdomyosarcoma / pathology

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  • [Copyright] (c) 2006 Wiley Periodicals, Inc.
  • (PMID = 16783829.001).
  • [ISSN] 1043-3074
  • [Journal-full-title] Head & neck
  • [ISO-abbreviation] Head Neck
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 39
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55. 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
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  • [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

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  • (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
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56. 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
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  • [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. Antigens, CD99. Cell Adhesion Molecules / analysis. Female. Humans. Immunohistochemistry. Male. Middle Aged

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  • (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 / Antigens, CD99; 0 / CD99 protein, human; 0 / Cell Adhesion Molecules
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57. Secondino S, Carrabba MG, Pedrazzoli P, Castagna L, Spina F, Grosso F, Bertuzzi A, Bay JO, Siena S, Corradini P, Niederwieser D, Demirer T, European Group for Blood and Marrow Transplantation Solid Tumors Working Party: Reduced intensity stem cell transplantation for advanced soft tissue sarcomas in adults: a retrospective analysis of the European Group for Blood and Marrow Transplantation. Haematologica; 2007 Mar;92(3):418-20
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  • We conducted a retrospective analysis on adult patients with advanced soft tissue sarcoma (STS) other than rhabdomyosarcoma who received allogeneic stem cell transplantation and were registered at the EBMT database.
  • [MeSH-major] Hematopoietic Stem Cell Transplantation / statistics & numerical data. Sarcoma / surgery. Transplantation Conditioning / methods
  • [MeSH-minor] Adult. Combined Modality Therapy. Disease Progression. Disease-Free Survival. Europe / epidemiology. Female. Follow-Up Studies. Graft Survival. Graft vs Host Disease / etiology. Graft vs Host Disease / mortality. Humans. Kaplan-Meier Estimate. Male. Middle Aged. Prognosis. Registries / statistics & numerical data. Remission Induction. Retrospective Studies. Transplantation, Homologous. Treatment Outcome. Vidarabine / administration & dosage. Vidarabine / analogs & derivatives

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  • (PMID = 17339195.001).
  • [ISSN] 1592-8721
  • [Journal-full-title] Haematologica
  • [ISO-abbreviation] Haematologica
  • [Language] eng
  • [Publication-type] Evaluation Studies; Journal Article; Multicenter Study
  • [Publication-country] Italy
  • [Chemical-registry-number] FA2DM6879K / Vidarabine; P2K93U8740 / fludarabine
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58. Jacobs JF, Brasseur F, Hulsbergen-van de Kaa CA, van de Rakt MW, Figdor CG, Adema GJ, Hoogerbrugge PM, Coulie PG, de Vries IJ: Cancer-germline gene expression in pediatric solid tumors using quantitative real-time PCR. Int J Cancer; 2007 Jan 1;120(1):67-74
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-minor] Adolescent. Adult. Bone Neoplasms / genetics. Bone Neoplasms / metabolism. Child. Child, Preschool. Humans. Immunoenzyme Techniques. Infant. Infant, Newborn. Male. Membrane Proteins / genetics. Membrane Proteins / metabolism. Neuroblastoma / genetics. Neuroblastoma / metabolism. Osteosarcoma / genetics. Osteosarcoma / metabolism. RNA, Messenger / metabolism. Reverse Transcriptase Polymerase Chain Reaction. Rhabdomyosarcoma / genetics. Rhabdomyosarcoma / metabolism. Sarcoma, Ewing / genetics. Sarcoma, Ewing / metabolism. Testis / metabolism

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  • (PMID = 17019710.001).
  • [ISSN] 0020-7136
  • [Journal-full-title] International journal of cancer
  • [ISO-abbreviation] Int. J. Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, Neoplasm; 0 / CTAG1B protein, human; 0 / GAGE2A protein, human; 0 / Membrane Proteins; 0 / Neoplasm Proteins; 0 / RNA, Messenger
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59. Kapels KM, Nishio J, Zhou M, Qualman SJ, Bridge JA: Embryonal rhabdomyosarcoma with a der(16)t(1;16) translocation. Cancer Genet Cytogenet; 2007 Apr 1;174(1):68-73
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  • [Title] Embryonal rhabdomyosarcoma with a der(16)t(1;16) translocation.
  • Embryonal rhabdomyosarcoma (ERMS) is the most common subtype of RMS that predominantly involves the genitourinary tract and the head and neck regions in children younger than 10 years of age.
  • [MeSH-major] Chromosomes, Human, Pair 1 / genetics. Chromosomes, Human, Pair 16 / genetics. Rhabdomyosarcoma, Embryonal / genetics. Translocation, Genetic
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Chromosome Banding. Female. Humans. Infant. Karyotyping. Male

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  • (PMID = 17350470.001).
  • [ISSN] 0165-4608
  • [Journal-full-title] Cancer genetics and cytogenetics
  • [ISO-abbreviation] Cancer Genet. Cytogenet.
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / CA36727; United States / NCI NIH HHS / CA / CA89461; United States / NCI NIH HHS / CA / CA98543
  • [Publication-type] Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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60. Hejazi N: Frameless image-guided neuronavigation in orbital surgery: practical applications. Neurosurg Rev; 2006 Apr;29(2):118-22
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  • A frameless infrared-based neuronavigation system (VectorVision, BrainLAB, Heimstetten, Germany) was used in the microsurgical removal of 11 orbital tumors (five cavernomas, three lymphomas, two dermoid tumors, and one rhabdomyosarcoma).
  • [MeSH-major] Dermoid Cyst / surgery. Hemangioma, Cavernous / surgery. Lymphoma / surgery. Neuronavigation. Orbital Neoplasms / surgery. Rhabdomyosarcoma / surgery. Surgery, Computer-Assisted
  • [MeSH-minor] Adult. Aged. Biopsy. Diagnosis, Differential. Female. Follow-Up Studies. Humans. Image Processing, Computer-Assisted. Imaging, Three-Dimensional. Magnetic Resonance Imaging. Male. Middle Aged. Orbit / pathology. Orbit / surgery. Postoperative Complications / etiology. Tomography, X-Ray Computed. Vision Disorders / etiology

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  • [Cites] Acta Neurochir (Wien). 2004 Apr;146(4):369-77; discussion 377 [15057531.001]
  • [Cites] Ophthalmologe. 1996 Oct;93(5):623-30 [9004891.001]
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  • (PMID = 16374647.001).
  • [ISSN] 0344-5607
  • [Journal-full-title] Neurosurgical review
  • [ISO-abbreviation] Neurosurg Rev
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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61. Maki RG, Kraft AS, Scheu K, Yamada J, Wadler S, Antonescu CR, Wright JJ, Schwartz GK: A multicenter Phase II study of bortezomib in recurrent or metastatic sarcomas. Cancer; 2005 Apr 1;103(7):1431-8
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  • Arm A included patients with osteogenic sarcoma, Ewing sarcoma, and rhabdomyosarcoma.
  • CONCLUSIONS: Bortezomib has minimal activity in soft tissue sarcoma as a single agent.
  • [MeSH-major] Antineoplastic Agents / therapeutic use. Bone Neoplasms / drug therapy. Boronic Acids / therapeutic use. Proteasome Inhibitors. Pyrazines / therapeutic use. Sarcoma / drug therapy. Soft Tissue Neoplasms / drug therapy
  • [MeSH-minor] Adult. Aged. Bortezomib. Drug Administration Schedule. Fatigue / chemically induced. Female. Humans. Male. Middle Aged. Neoplasm Metastasis / drug therapy. Neoplasm Recurrence, Local / drug therapy. Nervous System Diseases / chemically induced. Treatment Outcome

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  • [Copyright] Copyright 2005 American Cancer Society.
  • (PMID = 15739208.001).
  • [ISSN] 0008-543X
  • [Journal-full-title] Cancer
  • [ISO-abbreviation] Cancer
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CM / N01-CM17105; United States / NCI NIH HHS / CA / P01-CA47179
  • [Publication-type] Clinical Trial; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 0 / Boronic Acids; 0 / Proteasome Inhibitors; 0 / Pyrazines; 69G8BD63PP / Bortezomib
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62. Kopp HG, Patel S, Brücher B, Hartmann JT: Potential combination chemotherapy approaches for advanced adult-type soft-tissue sarcoma. Am J Clin Dermatol; 2008;9(4):207-17
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  • [Title] Potential combination chemotherapy approaches for advanced adult-type soft-tissue sarcoma.
  • However, a few subtypes, such as small round-cell tumors and rhabdomyosarcoma (other than pleomorphic), are considered chemotherapy sensitive.
  • In order to be successful, it may be necessary to combine not only different compounds but also different targets beyond the proliferation machinery of sarcoma cells such as tumor angiogenesis, the tumor stromal compartment, or tumor cell oncogene products.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Sarcoma / drug therapy. Soft Tissue Neoplasms / drug therapy
  • [MeSH-minor] Adult. Angiogenesis Inhibitors / administration & dosage. Anthracyclines / administration & dosage. Antibodies, Monoclonal / administration & dosage. Humans. Neoplasm Staging. Protein Kinase Inhibitors / administration & dosage

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  • (PMID = 18572972.001).
  • [ISSN] 1175-0561
  • [Journal-full-title] American journal of clinical dermatology
  • [ISO-abbreviation] Am J Clin Dermatol
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] New Zealand
  • [Chemical-registry-number] 0 / Angiogenesis Inhibitors; 0 / Anthracyclines; 0 / Antibodies, Monoclonal; 0 / Protein Kinase Inhibitors
  • [Number-of-references] 108
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63. Houghton JP, McCluggage WG: Embryonal rhabdomyosarcoma of the cervix with focal pleomorphic areas. J Clin Pathol; 2007 Jan;60(1):88-9
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  • [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


64. Pepek JM, Willett CG, Wu QJ, Yoo S, Clough RW, Czito BG: Intensity-modulated radiation therapy for anal malignancies: a preliminary toxicity and disease outcomes analysis. Int J Radiat Oncol Biol Phys; 2010 Dec 1;78(5):1413-9
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  • [MeSH-minor] Adenocarcinoma / radiotherapy. Adolescent. Adult. Aged. Aged, 80 and over. Anemia / etiology. Carcinoma, Squamous Cell / radiotherapy. Diarrhea / etiology. Female. Humans. Leukopenia / etiology. Male. Melanoma / radiotherapy. Middle Aged. Neuroendocrine Tumors / radiotherapy. Radiotherapy Dosage. Rhabdomyosarcoma / radiotherapy. Sarcoma / radiotherapy. Thrombocytopenia / etiology. Treatment Outcome. Young Adult

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  • [Copyright] Copyright © 2010 Elsevier Inc. All rights reserved.
  • (PMID = 20231064.001).
  • [ISSN] 1879-355X
  • [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
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65. Benesch M, Windelberg M, Sauseng W, Witt V, Fleischhack G, Lackner H, Gadner H, Bode U, Urban C: Compassionate use of bevacizumab (Avastin) in children and young adults with refractory or recurrent solid tumors. Ann Oncol; 2008 Apr;19(4):807-13
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  • PATIENTS AND METHODS: Fifteen patients (male: n = 8; female: n = 7; median age, 14.6 years) received bevacizumab for recurrent or progressive solid tumors (carcinoma: n = 3; neuroblastoma: n = 2; astrocytoma grade III: n = 2; rhabdomyosarcoma: n = 2; nephroblastoma: n = 2; benign vascular tumors: n = 2; synovial sarcoma: n = 1; and malignant hemangiopericytoma: n = 1) on a compassionate basis.
  • Radiographic objective responses (partial responses) were observed in two patients with astrocytoma grade III and in one patient each with neuroblastoma and pleomorphic rhabdomyosarcoma, respectively.

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  • (PMID = 18056650.001).
  • [ISSN] 1569-8041
  • [Journal-full-title] Annals of oncology : official journal of the European Society for Medical Oncology
  • [ISO-abbreviation] Ann. Oncol.
  • [Language] ENG
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Angiogenesis Inhibitors; 0 / Antibodies, Monoclonal; 0 / Antibodies, Monoclonal, Humanized; 2S9ZZM9Q9V / Bevacizumab
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66. Manarolla G, Radaelli E, Pisoni G, Sironi G, Rampin T: Rhabdomyosarcoma of the pectoral muscles of a free-living European robin (Erithacus rubecula). Avian Pathol; 2008 Jun;37(3):311-4
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  • [Title] Rhabdomyosarcoma of the pectoral muscles of a free-living European robin (Erithacus rubecula).
  • An adult free-living European robin (Erithacus rubecula) with a large, firm, subcutaneous mass on the pectoral muscle was examined.
  • The homogeneously positive immunolabelling for vimentin and scattered positivity for myoglobin and desmin suggested a diagnosis of rhabdomyosarcoma.
  • [MeSH-major] Bird Diseases / pathology. Muscle, Skeletal / pathology. Rhabdomyosarcoma / veterinary. Songbirds

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  • (PMID = 18568658.001).
  • [ISSN] 1465-3338
  • [Journal-full-title] Avian pathology : journal of the W.V.P.A
  • [ISO-abbreviation] Avian Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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67. Faisham WI, Zulmi W, Nor Azman MZ, Rhendra Hardy MZ: Forequarter amputation of the upper extremity for musculoskeletal tumors: posterior approach revisited. Med J Malaysia; 2006 Feb;61 Suppl A:57-61
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  • One patient had massive fungating squamous cell carcinoma and another had recurrent rhabdomyosarcoma.
  • [MeSH-minor] Adolescent. Adult. Female. Humans. Humerus / pathology. Humerus / surgery. Male. Posture. Prospective Studies. Scapula / pathology. Scapula / surgery

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  • (PMID = 17042232.001).
  • [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
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68. Gebert C, Hillmann A, Schwappach A, Hoffmann Ch, Hardes J, Kleinheinz J, Gosheger G: Free vascularized fibular grafting for reconstruction after tumor resection in the upper extremity. J Surg Oncol; 2006 Aug 1;94(2):114-27
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  • The indications for VFG were resection after osteosarcoma (9 cases), Ewings sarcoma (9 cases), chondrosarcoma (1 case), rhabdomyosarcoma (1 case), and 1 case of fibrous dysplasia.
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Chondrosarcoma / surgery. Female. Fibrous Dysplasia of Bone / surgery. Humans. Osteosarcoma / surgery. Range of Motion, Articular. Rhabdomyosarcoma / surgery. Sarcoma, Ewing / surgery. Treatment Outcome. Upper Extremity. Wound Healing


69. Lin Y, Zhu H, Liu J, Wang H: [Modified sternocleidomastoid myocutaneous flap for reconstruction of soft tissue defects following tumorectomy of maxillofacial region]. Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi; 2010 Apr;24(4):452-4
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  • There were 27 cases of well-differentiated squamous cell carcinoma (SC), 14 cases of poorly-differentiated SC, 1 case of rhabdomyosarcoma, and 1 case of adenoid cystic carcinoma.
  • [MeSH-minor] Adult. Aged. Female. Humans. Male. Middle Aged. Mouth Neoplasms / surgery. Reconstructive Surgical Procedures / methods

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  • (PMID = 20459009.001).
  • [ISSN] 1002-1892
  • [Journal-full-title] Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery
  • [ISO-abbreviation] Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Evaluation Studies; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] China
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70. Kremens B: [Systemic therapy in children and adolescents]. Urologe A; 2007 Oct;46(10):1404-6
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  • National and supranational treatment studies are the standard of care for pediatric cancer in Germany; they yield 5-year survival rates of almost 90% for nephroblastoma and germ cell tumors and 60% for neuroblastoma (all stages) and rhabdomyosarcoma.
  • The principles of antineoplastic therapy are the same as in adult cancer medicine; the drugs used depend upon the disease.
  • [MeSH-minor] Adolescent. Adrenal Gland Neoplasms / drug therapy. Adrenal Gland Neoplasms / mortality. Adrenal Gland Neoplasms / pathology. Adrenal Gland Neoplasms / surgery. Adrenal Medulla. Chemotherapy, Adjuvant. Child. Child, Preschool. Combined Modality Therapy. Humans. Infant. Kidney Neoplasms / drug therapy. Kidney Neoplasms / mortality. Kidney Neoplasms / pathology. Kidney Neoplasms / surgery. Neoplasm Staging. Neoplasms, Germ Cell and Embryonal / drug therapy. Neoplasms, Germ Cell and Embryonal / mortality. Neoplasms, Germ Cell and Embryonal / pathology. Neoplasms, Germ Cell and Embryonal / surgery. Neuroblastoma / drug therapy. Neuroblastoma / mortality. Neuroblastoma / pathology. Neuroblastoma / surgery. Prognosis. Radiotherapy, Adjuvant. Rhabdomyosarcoma / drug therapy. Rhabdomyosarcoma / mortality. Rhabdomyosarcoma / pathology. Rhabdomyosarcoma / surgery. Survival Rate. Wilms Tumor / drug therapy. Wilms Tumor / mortality. Wilms Tumor / pathology. Wilms Tumor / surgery

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  • (PMID = 17823786.001).
  • [ISSN] 0340-2592
  • [Journal-full-title] Der Urologe. Ausg. A
  • [ISO-abbreviation] Urologe A
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Germany
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71. Evans DG, Wu CL, Birch JM: BRCA2: a cause of Li-Fraumeni-like syndrome. J Med Genet; 2008 Jan;45(1):62-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-minor] Adult. Breast Neoplasms / genetics. Carcinoma, Basal Cell / genetics. Child. Child, Preschool. Female. Genes, Dominant. Humans. Incidence. Middle Aged. Pedigree. Rhabdomyosarcoma / genetics. Sarcoma / genetics

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  • [CommentOn] J Med Genet. 2001 Apr;38(4):253-7 [11370630.001]
  • (PMID = 18178637.001).
  • [ISSN] 1468-6244
  • [Journal-full-title] Journal of medical genetics
  • [ISO-abbreviation] J. Med. Genet.
  • [Language] eng
  • [Publication-type] Comment; Letter
  • [Publication-country] England
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72. Hume-Smith H, Fowler A, Vaz F, Suaris P: Dental implant removal to facilitate suspension laryngoscopy and laser treatment of an obstructed airway. Anaesthesia; 2010 Jan;65(1):78-81
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  • His past medical history included childhood nasolabial rhabdomyosarcoma treated by surgery, chemotherapy and radiotherapy.
  • [MeSH-minor] Adult. Combined Modality Therapy. Device Removal. Head and Neck Neoplasms / therapy. Humans. Male. Patient Care Team. Rhabdomyosarcoma / therapy

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  • [ErratumIn] Anaesthesia. 2010 Mar;65(3):324
  • (PMID = 19849679.001).
  • [ISSN] 1365-2044
  • [Journal-full-title] Anaesthesia
  • [ISO-abbreviation] Anaesthesia
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Dental Implants
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73. Abellar RG, Pepperell JR, Greco D, Gundogan F, Kostadinov S, Schwartz J, Tantravahi U, De Paepe ME: Effects of chemotherapy during pregnancy on the placenta. Pediatr Dev Pathol; 2009 Jan-Feb;12(1):35-41
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  • Patients (n = 13) underwent chemotherapy during pregnancy for carcinoma of breast (3), ovary (2), cervix (2), salivary gland (1), lymphoma/leukemia (4), or rhabdomyosarcoma (1).
  • In one case (rhabdomyosarcoma), the mother was exposed to cytotoxic agents throughout the entire pregnancy.
  • [MeSH-minor] Abnormalities, Multiple / chemically induced. Adolescent. Adult. Female. Humans. In Situ Hybridization, Fluorescence. Infant, Newborn. Pregnancy. Pregnancy Trimester, First. Pregnancy Trimester, Second. Pregnancy Trimester, Third. Retrospective Studies

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  • (PMID = 18462010.001).
  • [ISSN] 1093-5266
  • [Journal-full-title] Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
  • [ISO-abbreviation] Pediatr. Dev. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antineoplastic Agents
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74. Vergani L, Malena A, Sabatelli P, Loro E, Cavallini L, Magalhaes P, Valente L, Bragantini F, Carrara F, Leger B, Poulton J, Russell AP, Holt IJ: Cultured muscle cells display defects of mitochondrial myopathy ameliorated by anti-oxidants. Brain; 2007 Oct;130(Pt 10):2715-24
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  • To investigate the muscle-specific pathophysiology of mitochondrial disease, rhabdomyosarcoma transmitochondrial hybrid cells (cybrids) were generated that retain the capacity to differentiate to myotubes.
  • These data suggest that rhabdomyosarcoma cybrids are a valid cellular model for studying muscle-specific features of mitochondrial disease and that excess reactive oxygen species production is a significant contributor to mitochondrial dysfunction, which is amenable to anti-oxidant therapy.
  • [MeSH-minor] Adult. Animals. Cell Differentiation. Cells, Cultured. DNA, Mitochondrial / genetics. Gene Expression Regulation. Humans. Male. Microscopy, Electron. Mitochondria, Muscle / drug effects. Mitochondria, Muscle / ultrastructure. Muscle Fibers, Skeletal / metabolism. Oxidation-Reduction. Rats. Rats, Sprague-Dawley. Reactive Oxygen Species / metabolism. Tumor Cells, Cultured

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  • (PMID = 17626036.001).
  • [ISSN] 1460-2156
  • [Journal-full-title] Brain : a journal of neurology
  • [ISO-abbreviation] Brain
  • [Language] eng
  • [Grant] Italy / Telethon / / 1252; United Kingdom / Medical Research Council / / G0500695; United Kingdom / Medical Research Council / / MC/ U105663140
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antioxidants; 0 / DNA, Mitochondrial; 0 / Reactive Oxygen Species
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75. Bhurgri Y, Bhurgri H, Pervez S, Kayani N, Usman A, Bashir I, Bhurgri A, Hasan SH, Zaidi SM: Epidemiology of soft tissue sarcomas in Karachi South, Pakistan (1995-7). Asian Pac J Cancer Prev; 2008 Oct-Dec;9(4):709-14
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  • The most common histological tumor was rhabdomyosarcoma, though the occurrence of the histological subtypes was age-dependent.
  • CONCLUSION: Karachi falls into a high risk region for STS, observed in a relatively younger population, with a male predominance, high frequency of rhabdomyosarcoma and advanced stage at diagnosis.
  • [MeSH-major] Sarcoma / epidemiology. Sarcoma / pathology
  • [MeSH-minor] Adolescent. Adult. Age Distribution. Developing Countries. Female. Humans. Male. Middle Aged. Neoplasm Staging. Pakistan / epidemiology. Prevalence. Prognosis. Registries. Retrospective Studies. Sex Distribution. Survival Analysis. Young Adult

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  • (PMID = 19256764.001).
  • [ISSN] 2476-762X
  • [Journal-full-title] Asian Pacific journal of cancer prevention : APJCP
  • [ISO-abbreviation] Asian Pac. J. Cancer Prev.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Thailand
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76. Jarzembowski JA, Lieberman RW: Pediatric sex cord-stromal tumor with composite morphology: a case report. Pediatr Dev Pathol; 2005 Nov-Dec;8(6):680-4
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  • Histologically, the tumor exhibited several different morphologic appearances including adult granulosa cell tumor, juvenile granulosa cell tumor (with areas of marked atypia), and Sertoli cell tumor.
  • Together, these findings supported a diagnosis of mixed sex cord-stromal tumor including granulosa cell tumor of adult and juvenile types and intermediate- to high-grade Sertoli cell tumor, with large areas of markedly atypical sex cord-stromal tumor.
  • [MeSH-minor] Carcinoma, Small Cell / pathology. Child. Developmental Disabilities / complications. Diagnosis, Differential. Female. Humans. Immunohistochemistry. Intellectual Disability / complications. Lymphoma / pathology. Microscopy, Electron, Transmission. Neuroectodermal Tumors, Primitive / pathology. Rhabdomyosarcoma / pathology. Sarcoma, Ewing / pathology

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  • (PMID = 16222477.001).
  • [ISSN] 1093-5266
  • [Journal-full-title] Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
  • [ISO-abbreviation] Pediatr. Dev. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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77. Engelhardt M, Zeiser R, Ihorst G, Finke J, Müller CI: High-dose chemotherapy and autologous peripheral blood stem cell transplantation in adult patients with high-risk or advanced Ewing and soft tissue sarcoma. J Cancer Res Clin Oncol; 2007 Jan;133(1):1-11
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  • [Title] High-dose chemotherapy and autologous peripheral blood stem cell transplantation in adult patients with high-risk or advanced Ewing and soft tissue sarcoma.
  • PURPOSE: Despite the availability of combined-modality treatment for Ewing sarcoma (ES) and soft tissue sarcomas (STS), results from independent groups still indicate a poor prognosis for high-risk and metastasized patients.
  • METHODS: Here, we report of HDCT in 35 consecutive adult patients with poor-risk ES or rhabdomyosarcoma (n = 11) and STS (n = 24) undergoing ASCT between July 1992 and March 2003.
  • [MeSH-major] Antineoplastic Combined Chemotherapy Protocols / therapeutic use. Peripheral Blood Stem Cell Transplantation. Sarcoma / therapy. Sarcoma, Ewing / therapy
  • [MeSH-minor] Adult. Chemotherapy, Adjuvant. Drug Administration Schedule. Female. Follow-Up Studies. Humans. Male. Neoplasm Staging. Prognosis. Prospective Studies. Rhabdomyosarcoma / therapy. Risk Factors. Survival Analysis. Transplantation, Autologous. Treatment Outcome


78. Coindre JM: [Molecular diagnosis of routine sarcomas]. Ann Pathol; 2008 Nov;28 Spec No 1(1):S64-5
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  • [MeSH-major] Genetic Techniques. Sarcoma / diagnosis
  • [MeSH-minor] Adult. Biomarkers, Tumor / analysis. Biomarkers, Tumor / genetics. Bone Neoplasms / diagnosis. Bone Neoplasms / genetics. Bone Neoplasms / pathology. Child. Humans. Rhabdomyosarcoma, Alveolar / diagnosis. Rhabdomyosarcoma, Alveolar / genetics. Rhabdomyosarcoma, Alveolar / pathology. Sarcoma, Ewing / diagnosis. Sarcoma, Ewing / genetics. Sarcoma, Ewing / pathology. Sarcoma, Synovial / diagnosis. Sarcoma, Synovial / genetics. Sarcoma, Synovial / pathology. Soft Tissue Neoplasms / diagnosis. Soft Tissue Neoplasms / genetics. Soft Tissue Neoplasms / pathology

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  • (PMID = 18984305.001).
  • [ISSN] 0242-6498
  • [Journal-full-title] Annales de pathologie
  • [ISO-abbreviation] Ann Pathol
  • [Language] fre
  • [Publication-type] Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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79. 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
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  • [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

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  • (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
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80. 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
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  • [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

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  • (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
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81. 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
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  • [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

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  • [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
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82. Malagón HD, Valdez AM, Moran CA, Suster S: Germ cell tumors with sarcomatous components: a clinicopathologic and immunohistochemical study of 46 cases. Am J Surg Pathol; 2007 Sep;31(9):1356-62
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  • The SC included embryonal rhabdomyosarcoma (29), angiosarcoma (6), leiomyosarcoma (4), undifferentiated sarcoma (3), myxoid liposarcoma (1), malignant peripheral nerve sheath tumor (1), malignant "triton" tumor (1), and epithelioid hemangioendothelioma (1).
  • [MeSH-major] Immunohistochemistry. Mediastinal Neoplasms / diagnosis. Neoplasms, Germ Cell and Embryonal / diagnosis. Ovarian Neoplasms / diagnosis. Retroperitoneal Neoplasms / diagnosis. Sarcoma / diagnosis. Testicular Neoplasms / diagnosis
  • [MeSH-minor] Adolescent. Adult. Aged. Antineoplastic Combined Chemotherapy Protocols. Disease-Free Survival. Female. Follow-Up Studies. Humans. Male. Middle Aged. Neoplasm Metastasis. Neoplasm Staging. Orchiectomy. Ovariectomy. Time Factors. Treatment Outcome

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  • (PMID = 17721191.001).
  • [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
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83. Clerico A, Cappelli C, Ragni G, Caroli S, De Ioris MA, Sordi A, Petrucci F, Bocca B, Alimonti A: Evaluation of carboplatin pharmacokinetics in pediatric oncology by means of inductively coupled plasma mass spectrometry. Ann Ist Super Sanita; 2006;42(4):461-8
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  • [MeSH-minor] Adolescent. Adult. Area Under Curve. Brain Neoplasms / drug therapy. Child. Child, Preschool. Female. Humans. Male. Myosarcoma / drug therapy. Neoplasms, Muscle Tissue / drug therapy. Rhabdomyosarcoma / drug therapy

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  • Hazardous Substances Data Bank. CARBOPLATIN .
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  • (PMID = 17361071.001).
  • [ISSN] 0021-2571
  • [Journal-full-title] Annali dell'Istituto superiore di sanità
  • [ISO-abbreviation] Ann. Ist. Super. Sanita
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Italy
  • [Chemical-registry-number] 0 / Antineoplastic Agents; 49DFR088MY / Platinum; BG3F62OND5 / Carboplatin
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84. 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
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  • [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

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  • (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
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85. Wang Y, Zhu H, Zhao HP, Hei Y, Xiao LH: [Diagnosis and management of the tumors of extraocular muscles]. Zhonghua Yan Ke Za Zhi; 2009 Jan;45(1):56-60
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  • RESULTS: There were fibromatosis in 3 cases, intermuscular hemangioma and granular cell tumor both in 2 cases, inflammatory myofibroblastic tumor, rhabdomyosarcoma, T cell lymphoma and metastatic adenocarcinoma all in 1 case.
  • [MeSH-minor] Adolescent. Adult. Child. Child, Preschool. Female. Humans. Infant. Male. Middle Aged. Prognosis. Retrospective Studies. Young Adult

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  • (PMID = 19484932.001).
  • [ISSN] 0412-4081
  • [Journal-full-title] [Zhonghua yan ke za zhi] Chinese journal of ophthalmology
  • [ISO-abbreviation] Zhonghua Yan Ke Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
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86. Hayes-Jordan A, Stoner JA, Anderson JR, Rodeberg D, Weiner G, Meyer WH, Hawkins DS, Arndt CA, Paidas C, Children's Oncology Group: The impact of surgical excision in chest wall rhabdomyosarcoma: a report from the Children's Oncology Group. J Pediatr Surg; 2008 May;43(5):831-6
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  • [Title] The impact of surgical excision in chest wall rhabdomyosarcoma: a report from the Children's Oncology Group.
  • AIMS: Rhabdomyosarcoma (RMS) is the most common soft tissue tumor of childhood.
  • METHODS: A retrospective chart review was conducted of all 130 pediatric patients enrolled in the Intergroup Rhabdomyosarcoma Study (IRS) with chest wall rhabdomyosarcoma from the first (I) through fourth (IV) IRS with follow-up to June 2005.
  • [MeSH-major] Rhabdomyosarcoma / surgery. Thoracic Neoplasms / surgery. Thoracic Wall / surgery
  • [MeSH-minor] Adolescent. Adult. Chemotherapy, Adjuvant. Child. Child, Preschool. Disease-Free Survival. Female. Humans. Infant. Infant, Newborn. Male. Neoplasm Staging. Radiotherapy, Adjuvant. Retrospective Studies. Survival Rate. Treatment Outcome

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  • (PMID = 18485948.001).
  • [ISSN] 1531-5037
  • [Journal-full-title] Journal of pediatric surgery
  • [ISO-abbreviation] J. Pediatr. Surg.
  • [Language] eng
  • [Grant] United States / NCI NIH HHS / CA / U10 CA098413; United States / NCI NIH HHS / CA / U10 CA098543
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ NIHMS733105; NLM/ PMC4646069
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87. Andrade CR, Takahama Junior A, Nishimoto IN, Kowalski LP, Lopes MA: Rhabdomyosarcoma of the head and neck: a clinicopathological and immunohistochemical analysis of 29 cases. Braz Dent J; 2010 Jan;21(1):68-73
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  • [Title] Rhabdomyosarcoma of the head and neck: a clinicopathological and immunohistochemical analysis of 29 cases.
  • Rhabdomyosarcoma is a malignant tumor occurring more frequently in the childhood.
  • [MeSH-major] Head and Neck Neoplasms / epidemiology. Rhabdomyosarcoma / epidemiology
  • [MeSH-minor] Adolescent. Adult. Age Factors. Aged. Antigens, CD95 / analysis. Brazil / epidemiology. Child. Child, Preschool. Cyclin-Dependent Kinase 4 / analysis. Female. Humans. Immunohistochemistry. Infant. Ki-67 Antigen / analysis. Male. Meningeal Neoplasms / epidemiology. Middle Aged. Neoadjuvant Therapy. Neoplasm Staging. Orbital Neoplasms / epidemiology. Proliferating Cell Nuclear Antigen / analysis. Receptor, ErbB-2 / analysis. Retrospective Studies. Sex Factors. Survival Rate. Tumor Suppressor Protein p53 / analysis. Young Adult


88. Raney B, Anderson J, Breneman J, Donaldson SS, Huh W, Maurer H, Michalski J, Qualman S, Ullrich F, Wharam M, Meyer W, Soft-Tissue Sarcoma Committee of the Children's Oncology Group, Arcadia, California, USA: Results in patients with cranial parameningeal sarcoma and metastases (Stage 4) treated on Intergroup Rhabdomyosarcoma Study Group (IRSG) Protocols II-IV, 1978-1997: report from the Children's Oncology Group. Pediatr Blood Cancer; 2008 Jul;51(1):17-22
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  • [Title] Results in patients with cranial parameningeal sarcoma and metastases (Stage 4) treated on Intergroup Rhabdomyosarcoma Study Group (IRSG) Protocols II-IV, 1978-1997: report from the Children's Oncology Group.
  • PURPOSE: Determine outcome of patients with cranial parameningeal sarcoma and concurrent metastases treated on Intergroup Rhabdomyosarcoma Study Group (IRSG) Protocols II-IV.
  • PATIENTS: We identified 91 patients in the database, which includes newly diagnosed subjects <21 years old with rhabdomyosarcoma (RMS) and undifferentiated sarcoma, and reviewed their charts in detail.
  • CONCLUSIONS: Cure was possible for some patients with metastatic cranial parameningeal sarcoma.

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  • [Copyright] (c) 2008 Wiley-Liss, Inc.
  • (PMID = 18266224.001).
  • [ISSN] 1545-5017
  • [Journal-full-title] Pediatric blood & cancer
  • [ISO-abbreviation] Pediatr Blood Cancer
  • [Language] ENG
  • [Grant] United States / NCI NIH HHS / CA / CA-98543; United States / NCI NIH HHS / CA / CA-24507; United States / NCI NIH HHS / CA / U10 CA098413; United States / NCI NIH HHS / CA / CA-72989; United States / NCI NIH HHS / CA / U10 CA098543; United States / NCI NIH HHS / CA / CA-29511
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural
  • [Publication-country] United States
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89. 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
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  • [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

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  • (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
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90. 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
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  • [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

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  • (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
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91. 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
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  • [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


92. Hemalatha AL, Karthikeyan TM, Bharatnur SS, Kumar AS: Malignant peripheral nerve sheath tumor in oral cavity--a rare site. Indian J Pathol Microbiol; 2006 Jul;49(3):397-9
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  • Histopathological examination of the excised mass showed features of spindle cell sarcoma following which a provisional diagnosis of MPNST was offered.
  • The differential diagnosis considered were leiomyosarcoma, rhabdomyosarcoma and spindle cell variant of squamous cell carcinoma (being the commoner tumour in oral cavity).
  • [MeSH-minor] Adult. Diagnosis, Differential. Female. Humans

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  • (PMID = 17001897.001).
  • [ISSN] 0377-4929
  • [Journal-full-title] Indian journal of pathology & microbiology
  • [ISO-abbreviation] Indian J Pathol Microbiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
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93. Koksal Y, Sahin M, Koksal H, Esen H, Sen M: Neurofibroma adjacent to the thyroid gland and a thyroid papillary carcinoma in a patient with neurofibromatosis type 1: report of a case. Surg Today; 2009;39(10):884-7
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  • Some tumors may develop in these patients, including optic pathway gliomas, astrocytomas, brainstem gliomas, chronic myeloid leukemia, and rhabdomyosarcoma.
  • [MeSH-minor] Adult. Female. Humans. Neurofibroma / pathology. Treatment Outcome


94. Lüdike A, Knolle J, Schön R, Hinze P, Hofmann HS, Schreiber J: [Primary pulmonary rhabdomyosarcoma as a rare differential diagnosis of small cell lung cancer]. Pneumologie; 2005 Jul;59(7):456-60
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  • [Title] [Primary pulmonary rhabdomyosarcoma as a rare differential diagnosis of small cell lung cancer].
  • Primary pulmonary rhabdomyosarcoma is a rare entity and the histological differential diagnosis can be difficult.
  • Bronchial biopsies again showed a small cell tumor, although immunohistochemistry proved it to be a pleomorphic rhabdomyosarcoma.
  • The patient died from metastatic primary rhabdomyosarcoma of the lung.
  • [MeSH-major] Carcinoma, Small Cell / pathology. Lung Neoplasms / pathology. Rhabdomyosarcoma / pathology
  • [MeSH-minor] Adult. Combined Modality Therapy. Diagnosis, Differential. Fatal Outcome. Female. Humans. Recurrence

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  • (PMID = 16047279.001).
  • [ISSN] 0934-8387
  • [Journal-full-title] Pneumologie (Stuttgart, Germany)
  • [ISO-abbreviation] Pneumologie
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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95. 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
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  • [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

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  • (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
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96. Shrader MW, Schwab JH, Shaughnessy WJ, Jacofsky DJ: Pathologic femoral neck fractures in children. Am J Orthop (Belle Mead NJ); 2009 Feb;38(2):83-6; discussion 86
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  • Until now, all reported cases have been isolated cases, small series, or cases reported in series of adult pathologic hip fractures.
  • The pathologic diagnoses were fibrous dysplasia (5 children), unicameral bone cyst (2), Ewing's sarcoma (2), osteomyelitis (2), leukemia (1), rhabdomyosarcoma (1), osteogenesis imperfecta (1), and osteopetrosis (1).

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  • (PMID = 19340370.001).
  • [ISSN] 1934-3418
  • [Journal-full-title] American journal of orthopedics (Belle Mead, N.J.)
  • [ISO-abbreviation] Am J. Orthop.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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97. Lezrek M, Skiker H, Tachfouti S, Karim A, Karmane A, Bencherif Z, Cherkaoui W, Mohcine Z: [Orbital primitive neuroectodermal tumor with intracranial extension. A case report]. J Fr Ophtalmol; 2005 Nov;28(9):982
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  • We present a case of a young patient with orbital PNET extending to the endo-crane and sinuses, which had been treated 10 years before with the diagnosis of rhabdomyosarcoma.
  • [MeSH-minor] Adult. Humans. Male. Neoplasm Invasiveness

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  • (PMID = 16395214.001).
  • [ISSN] 1773-0597
  • [Journal-full-title] Journal français d'ophtalmologie
  • [ISO-abbreviation] J Fr Ophtalmol
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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98. 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
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  • [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

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  • (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
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99. Davidson DF: Elevated urinary dopamine in adults and children. Ann Clin Biochem; 2005 May;42(Pt 3):200-7
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  • In children, high urine dopamine was found in cases of neuroblastoma, Costello syndrome, leukaemia, phaeochromocytoma, Menkes disease and rhabdomyosarcoma of the bladder.
  • CONCLUSIONS: A high urine dopamine was found in <3% of adult urine specimens.
  • [MeSH-minor] Adrenal Gland Neoplasms / urine. Adult. Antidepressive Agents / therapeutic use. Catecholamines / urine. Child. Dihydroxyphenylalanine / therapeutic use. Female. Humans. Leukemia / urine. Male. Neuroblastoma / urine. Pheochromocytoma / urine. Pregnancy. Reference Values. Retrospective Studies. Specimen Handling / methods

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  • (PMID = 15949155.001).
  • [ISSN] 0004-5632
  • [Journal-full-title] Annals of clinical biochemistry
  • [ISO-abbreviation] Ann. Clin. Biochem.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antidepressive Agents; 0 / Catecholamines; 63-84-3 / Dihydroxyphenylalanine; VTD58H1Z2X / Dopamine
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100. Thomas-de-Montpréville V, Nottin R, Dulmet E, Serraf A: Heart tumors in children and adults: clinicopathological study of 59 patients from a surgical center. Cardiovasc Pathol; 2007 Jan-Feb;16(1):22-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Fibroma / pathology. Heart Neoplasms / pathology. Myxoma / pathology. Rhabdomyoma / pathology. Rhabdomyosarcoma / pathology. Sarcoma / pathology
  • [MeSH-minor] Adolescent. Adult. Aged. Echocardiography. Female. Humans. Infant. Infant, Newborn. Magnetic Resonance Imaging. Male. Middle Aged. Neoplasm Metastasis. Neoplasm Regression, Spontaneous. Retrospective Studies

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  • (PMID = 17218211.001).
  • [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] Journal Article
  • [Publication-country] United States
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