[X] Close
You are about to erase all the values you have customized, search history, page format, etc.
Click here to RESET all values       Click here to GO BACK without resetting any value
Items 1 to 100 of about 358
1. Nong D, Tang A, Xu Z, Nong H, Liang Y, Wang D, Li Y: [Clinical study of juvenile nasopharyngeal angiofibroma]. Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2006 Jan;20(2):70-2
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Clinical study of juvenile nasopharyngeal angiofibroma].
  • OBJECTIVE: To present our experiences of diagnosis and treatment for juvenile nasopharyngeal angiofibroma (JNA) and to evaluate the factors influencing intra-operative bleeding and tumor recurrence.
  • [MeSH-major] Angiofibroma / pathology. Nasopharyngeal Neoplasms / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16570817.001).
  • [Journal-full-title] Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology
  • [ISO-abbreviation] Lin Chuang Er Bi Yan Hou Ke Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] China
  •  go-up   go-down


2. Finis D, Gümbel H: [Central retinal artery occlusion after embolization in juvenile nasopharyngeal angiofibroma]. Klin Monbl Augenheilkd; 2009 Jul;226(7):579-80
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Central retinal artery occlusion after embolization in juvenile nasopharyngeal angiofibroma].
  • [MeSH-major] Angiofibroma / therapy. Embolization, Therapeutic / adverse effects. Nasopharyngeal Neoplasms / therapy. Retinal Artery Occlusion / etiology. Retinal Artery Occlusion / surgery

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19644808.001).
  • [ISSN] 1439-3999
  • [Journal-full-title] Klinische Monatsblätter für Augenheilkunde
  • [ISO-abbreviation] Klin Monbl Augenheilkd
  • [Language] ger
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


3. Tosun F, Onerci M, Durmaz A, Ugurel S: Spontaneous involution of nasopharyngeal angiofibroma. J Craniofac Surg; 2008 Nov;19(6):1686-9
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Spontaneous involution of nasopharyngeal angiofibroma.
  • There are several studies addressing regression of residual nasopharyngeal angiofibroma after surgery, but spontaneous regression of this tumor has been reported in only 2 cases.
  • We present a case of nasopharyngeal angiofibroma that has involuted spontaneously in the last 5 years.
  • This is the third reported case in the literature with spontaneous regression of nasopharyngeal angiofibroma.
  • [MeSH-major] Angiofibroma / pathology. Nasopharyngeal Neoplasms / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19098582.001).
  • [ISSN] 1536-3732
  • [Journal-full-title] The Journal of craniofacial surgery
  • [ISO-abbreviation] J Craniofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


Advertisement
4. Koshy S, George M, Gupta A, Daniel RT: Extended osteoplastic maxillotomy for total excision of giant multicompartmental juvenile nasopharyngeal angiofibroma. Indian J Dent Res; 2008 Oct-Dec;19(4):366-9
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Extended osteoplastic maxillotomy for total excision of giant multicompartmental juvenile nasopharyngeal angiofibroma.
  • Juvenile nasopharyngeal angiofibroma (JNA) is a rare vascular neoplasm occurring almost exclusively in adolescent males.
  • Although benign, it is often locally aggressive and can erode into surrounding tissues and structures resulting in significant morbidity and mortality.
  • In this paper, we report on the total excision of a large, recurrent JNA with intracranial extension into the middle cranial fossa encroaching into the cavernous sinus, by right temporal craniotomy and extended osteoplastic maxillotomy.
  • [MeSH-major] Angiofibroma / surgery. Maxilla / surgery. Nasopharyngeal Neoplasms / surgery. Neoplasm Recurrence, Local / surgery. Osteotomy / methods

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19075445.001).
  • [ISSN] 0970-9290
  • [Journal-full-title] Indian journal of dental research : official publication of Indian Society for Dental Research
  • [ISO-abbreviation] Indian J Dent Res
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
  •  go-up   go-down


5. Glad H, Vainer B, Buchwald C, Petersen BL, Theilgaard SA, Bonvin P, Lajer C, Jakobsen J: Juvenile nasopharyngeal angiofibromas in Denmark 1981-2003: diagnosis, incidence, and treatment. Acta Otolaryngol; 2007 Mar;127(3):292-9
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Juvenile nasopharyngeal angiofibromas in Denmark 1981-2003: diagnosis, incidence, and treatment.
  • CONCLUSIONS: Juvenile nasopharyngeal angiofibroma (JNA) is a rare tumor in young males, with a non-negligible potential for recurrence.
  • [MeSH-major] Angiofibroma / diagnosis. Nasopharyngeal Neoplasms / diagnosis

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17364367.001).
  • [ISSN] 0001-6489
  • [Journal-full-title] Acta oto-laryngologica
  • [ISO-abbreviation] Acta Otolaryngol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Norway
  •  go-up   go-down


6. Hunt CH, Morris JM, Lee PU, Cloft H: Progressive epistaxis in two young males: Classic presentations of juvenile nasopharyngeal angiofibroma in unusual locations. Neuroradiology; 2010 May;52(5):419-20
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Progressive epistaxis in two young males: Classic presentations of juvenile nasopharyngeal angiofibroma in unusual locations.
  • [MeSH-major] Angiofibroma / diagnostic imaging. Epistaxis / etiology. Nasopharyngeal Neoplasms / diagnostic imaging

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Ann Surg. 1948 Mar;127(3):513-36 [17859097.001]
  • [Cites] Laryngoscope. 1992 Aug;102(8):928-33 [1323003.001]
  • [Cites] Indian J Dent Res. 2004 Oct-Dec;15(4):145-8 [16035644.001]
  • [Cites] Laryngoscope. 2002 Jul;112(7 Pt 1):1213-20 [12169902.001]
  • [Cites] Laryngoscope. 1988 Feb;98(2):170-5 [3339927.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 2006 Sep;70(9):1619-27 [16777240.001]
  • (PMID = 20127084.001).
  • [ISSN] 1432-1920
  • [Journal-full-title] Neuroradiology
  • [ISO-abbreviation] Neuroradiology
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Germany
  •  go-up   go-down


7. Gupta AK, Purkayastha S, Bodhey NK, Kapilamoorthy TR, Kesavadas C: Preoperative embolization of hypervascular head and neck tumours. Australas Radiol; 2007 Oct;51(5):446-52
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • One patient (carotid body tumour) developed mild unilateral seventh, ninth and 10th cranial nerve palsy after transarterial embolization, transient hemiparesis was seen in another patient (nasopharyngeal angiofibroma).

  • MedlinePlus Health Information. consumer health - Head and Neck Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17803797.001).
  • [ISSN] 0004-8461
  • [Journal-full-title] Australasian radiology
  • [ISO-abbreviation] Australas Radiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Australia
  •  go-up   go-down


8. Fuleihan Gel-H, Rubeiz N: Dermatologic manifestations of parathyroid-related disorders. Clin Dermatol; 2006 Jul-Aug;24(4):281-8
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • In multiple endocrine neoplasia 1, patients commonly have angiofibromas (85%) and collagenomas (70%), lesions that show loss of one 11q13 allele, the molecular abnormality in multiple endocrine neoplasia 1.
  • Pseudohypoparathyroidism, an inherited disorder with end-organ unresponsiveness to parathyroid hormone, is characterized by Albright hereditary osteodystrophy.
  • [MeSH-major] Multiple Endocrine Neoplasia. Parathyroid Diseases. Skin Neoplasms

  • MedlinePlus Health Information. consumer health - Parathyroid Disorders.
  • MedlinePlus Health Information. consumer health - Skin Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16828410.001).
  • [ISSN] 0738-081X
  • [Journal-full-title] Clinics in dermatology
  • [ISO-abbreviation] Clin. Dermatol.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 43
  •  go-up   go-down


9. Robson CD: Imaging of head and neck neoplasms in children. Pediatr Radiol; 2010 Apr;40(4):499-509
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The characteristic imaging appearance for a variety of common and/or important pediatric head and neck tumors will be described in this review.
  • These include benign masses such as hemangioma, teratoma, nerve sheath tumors, juvenile nasopharyngeal angiofibroma and malignant masses such as rhabdomyosarcoma, lymphoma, carcinoma and retinoblastoma.

  • MedlinePlus Health Information. consumer health - Diagnostic Imaging.
  • MedlinePlus Health Information. consumer health - Head and Neck Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Oncologist. 2007 Oct;12(10):1237-46 [17962617.001]
  • [Cites] Oral Oncol. 2002 Jul;38(5):450-9 [12110339.001]
  • [Cites] Am J Med Genet A. 2006 May 1;140(9):975-86 [16575892.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 1987 Oct;13(3):279-92 [3679684.001]
  • [Cites] J Craniomaxillofac Surg. 1988 Aug;16(6):279-86 [3049677.001]
  • [Cites] Curr Probl Surg. 2000 Aug;37(8):517-84 [10955029.001]
  • [Cites] Nature. 1986 Oct 16-22;323(6089):643-6 [2877398.001]
  • [Cites] Head Neck. 2008 Mar;30(3):390-400 [18228521.001]
  • [Cites] Ultrasound Med Biol. 2000 Sep;26(7):1089-97 [11053743.001]
  • [Cites] Curr Opin Pediatr. 2008 Feb;20(1):23-9 [18197035.001]
  • [Cites] Appl Immunohistochem Mol Morphol. 2008 Mar;16(2):173-8 [18227724.001]
  • [Cites] Am J Surg Pathol. 2005 May;29(5):700-6 [15832097.001]
  • [Cites] Radiology. 1998 Jun;207(3):601-7 [9609880.001]
  • [Cites] Semin Nucl Med. 2007 Sep;37(5):316-31 [17707239.001]
  • [Cites] Radiol Clin North Am. 2008 Mar;46(2):313-38, ix [18619383.001]
  • [Cites] Arch Dermatol. 1996 Mar;132(3):307-11 [8607636.001]
  • [Cites] Am J Med Genet. 1994 Aug 15;52(2):130-5 [7801997.001]
  • [Cites] Cancer Invest. 2008 Apr-May;26(3):306-16 [18317972.001]
  • [Cites] J Clin Pathol. 2010 Jun;63(6):492-6 [18552174.001]
  • [Cites] Leuk Lymphoma. 2007 Apr;48(4):699-707 [17454627.001]
  • [Cites] Am J Pathol. 2009 Feb;174(2):550-64 [19147825.001]
  • [Cites] AJNR Am J Neuroradiol. 2010 Feb;31(2):257-61 [19779003.001]
  • (PMID = 20225112.001).
  • [ISSN] 1432-1998
  • [Journal-full-title] Pediatric radiology
  • [ISO-abbreviation] Pediatr Radiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


10. Bonnet ML, Aronica C, Chastanet G, Pilet G, Luneau D, Mathonière C, Clérac R, Robert V: Nickel(II) chain with alternating end-on/end-to-end single azido bridges: a combined structural, magnetic, and theoretical study. Inorg Chem; 2008 Feb 4;47(3):1127-33
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The reaction of a tridentate Schiff base LH (L-: 1,1,1-trifluoro-7-(dimethylamino)-4-methyl-5-aza-3-hepten-2-onato) with a Ni(II) salt in the presence of azide salt has led to a new alternating end-on (EO)/end-to-end (EE) azido-bridged Ni(II) chain of formula {[Ni2(micro1,1-N3)(micro1,3-N3)(L)2(MeOH)2]}n.
  • Magnetic susceptibility and magnetization measurements have been performed and revealed that the chain can magnetically be depicted as isolated {Ni2(N3)} units exhibiting antiferromagnetic interaction (JAF approximately -37 cm(-1)).

  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18161966.001).
  • [ISSN] 0020-1669
  • [Journal-full-title] Inorganic chemistry
  • [ISO-abbreviation] Inorg Chem
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


11. Li Z, Lin C, Lin G, Fang Z, Zhang H, Chen M, Zhou A, Lan S, Yi Z: [Study and analysis on the hemorrhage of pterygoid venous plexus in large nasopharyngeal angiofibroma resection]. Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2010 Mar;24(6):244-6, 249
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Study and analysis on the hemorrhage of pterygoid venous plexus in large nasopharyngeal angiofibroma resection].
  • OBJECTIVE: To our knowledge, study of the intraoperative profuse bleeding of pterygoid venous plexus (PVP) in large nasopharyngeal angiofibroma resection has not yet been reported.
  • Twenty-six of 44 cases were large nasopharyngeal angiofibromas according to the Fisch classification system(Fisch type III 16, type IV 10).
  • Factors influencing intraoperative bleeding of 26 large nasopharyngeal angiofibroma resections were analyzed retrospectively.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Veins / surgery

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20518285.001).
  • [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] Case Reports; English Abstract; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] China
  •  go-up   go-down


12. Kösling S, Knipping S, Hofmockel T: [Imaging of nasopharyngeal diseases]. Radiologe; 2009 Jan;49(1):17-26
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Imaging of nasopharyngeal diseases].
  • These include nasopharyngeal cysts, lymphoid hyperplasia, juvenile angiofibroma, carcinomas and non-Hodgkin lymphoma.
  • Typical radiological findings, possibilities for making a specific diagnosis, differential diagnosis and description of the spread of a neoplasm are the central points.
  • [MeSH-major] Magnetic Resonance Imaging. Nasopharyngeal Diseases / diagnosis. Nasopharyngeal Neoplasms / diagnosis. Tomography, X-Ray Computed
  • [MeSH-minor] Cysts / diagnosis. Cysts / pathology. Humans. Hyperplasia / diagnosis. Incidental Findings. Lymphoma, Non-Hodgkin / diagnosis. Lymphoma, Non-Hodgkin / pathology. Nasopharynx / pathology. Neoplasm Staging. Palatine Tonsil / pathology

  • MedlinePlus Health Information. consumer health - CT Scans.
  • MedlinePlus Health Information. consumer health - MRI Scans.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Br J Radiol. 2007 Jul;80(955):e145-6 [17704311.001]
  • [Cites] Acta Radiol. 2000 Nov;41(6):585-93 [11092480.001]
  • [Cites] Eur Radiol. 2007 Mar;17(3):852-3 [16710663.001]
  • [Cites] Br J Radiol. 1999 Feb;72 (854):204-6 [10365075.001]
  • [Cites] AJNR Am J Neuroradiol. 2000 Jun-Jul;21(6):1119-21 [10871025.001]
  • [Cites] Clin Otolaryngol Allied Sci. 1986 Aug;11(4):247-59 [3028678.001]
  • [Cites] AJR Am J Roentgenol. 1992 Sep;159(3):581-9 [1503031.001]
  • [Cites] AJNR Am J Neuroradiol. 1995 Oct;16(9):1936-8 [8693998.001]
  • [Cites] Eur J Radiol. 2002 Nov;44(2):82-95 [12413677.001]
  • [Cites] AJNR Am J Neuroradiol. 1999 Jun-Jul;20(6):1133-9 [10445457.001]
  • [Cites] Eur Radiol. 2007 Oct;17 (10 ):2622-30 [17404741.001]
  • [Cites] Radiographics. 2006 Jul-Aug;26(4):1169-85 [16844940.001]
  • [Cites] AJR Am J Roentgenol. 1992 Sep;159(3):601-7 [1503034.001]
  • [Cites] AJNR Am J Neuroradiol. 2003 Feb;24(2):279-82 [12591649.001]
  • [Cites] Australas Radiol. 2007 Jun;51(3):236-9 [17504314.001]
  • [Cites] Eur Radiol. 2006 Oct;16(10):2249-58 [16639497.001]
  • [Cites] AJR Am J Roentgenol. 2003 Jun;180(6):1715-22 [12760949.001]
  • (PMID = 19023557.001).
  • [ISSN] 1432-2102
  • [Journal-full-title] Der Radiologe
  • [ISO-abbreviation] Radiologe
  • [Language] ger
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 21
  •  go-up   go-down


13. Borghei P, Baradaranfar MH, Borghei SH, Sokhandon F: Transnasal endoscopic resection of juvenile nasopharyngeal angiofibroma without preoperative embolization. Ear Nose Throat J; 2006 Nov;85(11):740-3, 746
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Transnasal endoscopic resection of juvenile nasopharyngeal angiofibroma without preoperative embolization.
  • Juvenile nasopharyngeal angiofibroma (JNA) is a benign, highly vascular, and locally invasive tumor.
  • [MeSH-major] Angiofibroma / surgery. Endoscopy / methods. Nasopharyngeal Neoplasms / surgery

  • MedlinePlus Health Information. consumer health - Endoscopy.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17168151.001).
  • [ISSN] 0145-5613
  • [Journal-full-title] Ear, nose, & throat journal
  • [ISO-abbreviation] Ear Nose Throat J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


14. Sun W, Huang X, Zheng Y, Peng J, Zou H: [Resection of nasopharyngeal angiofibroma using by midfacial degloving approach and modified maxillectomy]. Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Dec;21(24):1134-5, 1139
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Resection of nasopharyngeal angiofibroma using by midfacial degloving approach and modified maxillectomy].
  • OBJECTIVE: To explore the feasibility of treatment on angiofibroma patients with stage III, IV by midfacial degloving approach and modified maxillectomy.
  • 2004, midfacial degloving approach and modified maxillectomy was used for treating 7 angiofibroma patients with stage III, IV.
  • The pathology of 7 cases was nasopharyngeal angiofibroma.
  • [MeSH-major] Angiofibroma / surgery. Maxilla / surgery. Nasopharyngeal Neoplasms / surgery

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18330264.001).
  • [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; Evaluation Studies; Journal Article
  • [Publication-country] China
  •  go-up   go-down


15. Khalifa MA, Ragab SM: Endoscopic assisted antral window approach for type III nasopharyngeal angiofibroma with infratemporal fossa extension. Int J Pediatr Otorhinolaryngol; 2008 Dec;72(12):1855-60
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Endoscopic assisted antral window approach for type III nasopharyngeal angiofibroma with infratemporal fossa extension.
  • OBJECTIVES: To assess the efficacy and safety of endoscopic assisted antral window approach in advanced nasopharyngeal angiofibroma with infratemporal fossa extension.
  • MATERIALS AND METHODS: Sixteen cases diagnosed as juvenile nasopharyngeal angiofibroma type III with infratemporal fossa extension were surgically managed using endoscopic assisted antral window approach (group A) and compared with another group of similar number that were managed using endoscopic assisted midfacial degloving (group B).
  • [MeSH-major] Angiofibroma / surgery. Cranial Fossa, Middle / pathology. Endoscopy / methods. Nasopharyngeal Neoplasms / surgery

  • MedlinePlus Health Information. consumer health - Endoscopy.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18952302.001).
  • [ISSN] 0165-5876
  • [Journal-full-title] International journal of pediatric otorhinolaryngology
  • [ISO-abbreviation] Int. J. Pediatr. Otorhinolaryngol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Ireland
  •  go-up   go-down


16. Hernández Monge A, Estrada Moscoso I, Márquez Iribe P, Alanis Fuentes J, Pacheco Pineda R: [Vulvar cellular angiofibroma. A report of a case and bibliographic review]. Ginecol Obstet Mex; 2006 Sep;74(9):499-502
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Vulvar cellular angiofibroma. A report of a case and bibliographic review].
  • [Transliterated title] Angiofibroma celular de la vulva. Comunicación de un caso y revisión de la bibliografía.
  • The vulvar cellular angiofibroma is a rare mesenchymal tumor.
  • Misdiagnosis is common and it can be confounded with spindle cell lipoma, hydrocele of the canal of Nuck, fibromas, angiomyofibroblastoma and many other mesenchymal tumors.
  • [MeSH-major] Angiofibroma / pathology. Vulvar Neoplasms / pathology

  • MedlinePlus Health Information. consumer health - Vulvar Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17133966.001).
  • [ISSN] 0300-9041
  • [Journal-full-title] Ginecología y obstetricia de México
  • [ISO-abbreviation] Ginecol Obstet Mex
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Mexico
  •  go-up   go-down


17. Porras Alonso EC, Benito Navarro JR, Fernandez Roche JA, Rodriguez Fernández-Freire A: [Child nasopharyngeal angiofibroma]. An Otorrinolaringol Ibero Am; 2005;32(5):483-90
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Child nasopharyngeal angiofibroma].
  • [Transliterated title] Angiofibroma nasofaringeo infantil.
  • Angiofibromas are benign tumors, highly vascularized, that affect male adolescents and young men.
  • We present a clinical case of an 11-year-old patient with an angiofibroma of the nasopharynx, reviewing the etiopathogenic theories and current surgical approaches.
  • [MeSH-major] Angiofibroma / pathology. Angiofibroma / radiography. Nasopharyngeal Neoplasms / pathology. Nasopharyngeal Neoplasms / radiography

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16318092.001).
  • [ISSN] 0303-8874
  • [Journal-full-title] Anales otorrinolaringológicos ibero-americanos
  • [ISO-abbreviation] An Otorrinolaringol Ibero Am
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
  •  go-up   go-down


18. Valencia MP, Castillo M: Congenital and acquired lesions of the nasal septum: a practical guide for differential diagnosis. Radiographics; 2008 Jan-Feb;28(1):205-24; quiz 326
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Inflammatory diseases that may affect the nasal septum include sarcoidosis, reparative granuloma, and Wegener granulomatosis.
  • Last, the tumors that may arise in the nasal septum or may involve it secondarily include carcinomas, Pindborg tumor, sarcoma, angiofibroma, hemangioma, neuroendocrine tumor, and schwannoma.

  • MedlinePlus Health Information. consumer health - Nasal Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18203939.001).
  • [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
  • [Number-of-references] 40
  •  go-up   go-down


19. Zhang QX, Ye J, Zhang SM, Li M: [Endoscopic nasal surgery in the treatment of nasopharyngeal angiofibroma]. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2005 Mar;40(3):222-3
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Endoscopic nasal surgery in the treatment of nasopharyngeal angiofibroma].
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15952579.001).
  • [ISSN] 1673-0860
  • [Journal-full-title] Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
  • [ISO-abbreviation] Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
  • [Language] chi
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] China
  •  go-up   go-down


20. Pérez LP, Zulaica A, Rodríguez L, Campo MC, Peñaranda JM, Fernández-Redondo V, Toribio J: Multinucleate cell angiohistiocytoma. Report of five cases. J Cutan Pathol; 2006 May;33(5):349-52
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Multinucleate cell angiohistiocytoma is an infrequent and most likely non-neoplastic disorder usually seen in acral regions in elderly women.
  • It must be distinguished from other diverse cutaneous lesions, notably dermatofibroma, Kaposi sarcoma, and angiofibroma.
  • [MeSH-major] Histiocytoma / pathology. Skin / blood supply. Skin Diseases / pathology

  • MedlinePlus Health Information. consumer health - Skin Conditions.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16640541.001).
  • [ISSN] 0303-6987
  • [Journal-full-title] Journal of cutaneous pathology
  • [ISO-abbreviation] J. Cutan. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
  •  go-up   go-down


21. Pryor SG, Moore EJ, Kasperbauer JL: Endoscopic versus traditional approaches for excision of juvenile nasopharyngeal angiofibroma. Laryngoscope; 2005 Jul;115(7):1201-7
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Endoscopic versus traditional approaches for excision of juvenile nasopharyngeal angiofibroma.
  • OBJECTIVES: Juvenile nasopharyngeal angiofibroma (JNA) is an uncommon neoplasm originating in the nasopharynx.
  • [MeSH-major] Angiofibroma / surgery. Endoscopy / methods. Nasopharyngeal Neoplasms / surgery. Otorhinolaryngologic Surgical Procedures / methods

  • MedlinePlus Health Information. consumer health - Endoscopy.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15995507.001).
  • [ISSN] 0023-852X
  • [Journal-full-title] The Laryngoscope
  • [ISO-abbreviation] Laryngoscope
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


22. Dhingra K, Singhal N, Khurana N: Poorly differentiated squamous cell carcinoma coexisting with angiofibroma and spreading as intravascular emboli in its vessels. Acta Otolaryngol; 2006 Dec;126(12):1342-4
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Poorly differentiated squamous cell carcinoma coexisting with angiofibroma and spreading as intravascular emboli in its vessels.
  • We report a case of a 28-year-old male who presented with epistaxis and hyponasal speech.
  • A clinical and radiological diagnosis of nasopharyngeal angiofibroma was made.
  • A diagnosis of poorly differentiated carcinoma, possibly squamous, with extensive embolization in the vessels of angiofibroma was made.
  • [MeSH-major] Angiofibroma / pathology. Carcinoma, Squamous Cell / pathology. Nasopharyngeal Neoplasms / pathology. Neoplasms, Multiple Primary / pathology. Neoplastic Cells, Circulating / pathology

  • Genetic Alliance. consumer health - Carcinoma, Squamous Cell.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17101599.001).
  • [ISSN] 0001-6489
  • [Journal-full-title] Acta oto-laryngologica
  • [ISO-abbreviation] Acta Otolaryngol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Norway
  •  go-up   go-down


23. Wataya-Kaneda M, Katayama I: Dissociate expression of tuberous sclerosis complex 1 product hamartin in a skin and pulmonary lesion of a tuberous sclerosis complex. Hum Pathol; 2009 Mar;40(3):430-4
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Dissociate expression of tuberous sclerosis complex 1 product hamartin in a skin and pulmonary lesion of a tuberous sclerosis complex.
  • Tuberous sclerosis complex is a multisystemic disorder characterized by systemic hamartomas.
  • Her skin lesion (angiofibroma) expressed both hamartin and tuberin, but her pulmonary lesion did not express hamartin.
  • [MeSH-major] Angiofibroma / pathology. Genes, Tumor Suppressor. Lung Neoplasms / pathology. Lymphangioleiomyomatosis / pathology. Skin Neoplasms / pathology. Tuberous Sclerosis / pathology. Tumor Suppressor Proteins / metabolism

  • Genetic Alliance. consumer health - Tuberous sclerosis.
  • MedlinePlus Health Information. consumer health - Lung Cancer.
  • MedlinePlus Health Information. consumer health - Skin Cancer.
  • MedlinePlus Health Information. consumer health - Tuberous Sclerosis.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18835623.001).
  • [ISSN] 1532-8392
  • [Journal-full-title] Human pathology
  • [ISO-abbreviation] Hum. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Tumor Suppressor Proteins; 0 / tuberous sclerosis complex 1 protein; 4JG2LF96VF / tuberous sclerosis complex 2 protein
  •  go-up   go-down


24. Perić A, Baletić N, Cerović S, Vukomanović-Durdević B: Middle turbinate angiofibroma in an elderly woman. Vojnosanit Pregl; 2009 Jul;66(7):583-6
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Middle turbinate angiofibroma in an elderly woman.
  • BACKGROUND: Angiofibromas are histologically benign vascular tumors, originating from the nasopharynx, near by the area of sphenopalatine foramen.
  • Reports of primary extranasopharyngeal angiofibromas have appeared sporadically in the literature in English.
  • We present the first case of an elderly woman with tumor arising from the middle turbinate, diagnosed as angiofibroma.
  • After the endoscopic excision of the mass, postoperative pathohistological and immunohistochemical analysis confirmed the diagnosis of an angiofibroma.
  • CONCLUSION: Extranasopharyngeal angiofibromas arising from the nasal cavity are extremely rare tumors.
  • [MeSH-major] Angiofibroma / diagnosis. Nose Neoplasms / diagnosis. Turbinates

  • MedlinePlus Health Information. consumer health - Nasal Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19678585.001).
  • [ISSN] 0042-8450
  • [Journal-full-title] Vojnosanitetski pregled
  • [ISO-abbreviation] Vojnosanit Pregl
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Serbia
  •  go-up   go-down


25. Boo H, Hogg JP: Nasal cavity neoplasms: a pictorial review. Curr Probl Diagn Radiol; 2010 Mar-Apr;39(2):54-61
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Retrospective case review of pathologically and clinically proven nasal cavity neoplasms are shown with multiple modalities including computed tomography (CT), magnetic resonance imaging (MRI), and positron emission tomography/computed tomography (PET/CT) to illustrate the findings and complement a succinct review of this category of disease.
  • Examples include squamous cell cancer, adenoid cystic cancer, esthesioneuroblastoma, inverted papilloma, juvenile nasal angiofibroma, melanoma, lymphoma, sarcoma, and benign nasal histiocytoma.
  • [MeSH-minor] Angiofibroma / diagnosis. Carcinoma, Adenoid Cystic / diagnosis. Carcinoma, Squamous Cell / diagnosis. Chondrosarcoma / diagnosis. Diagnosis, Differential. Esthesioneuroblastoma, Olfactory / diagnosis. Histiocytoma, Benign Fibrous / diagnosis. Humans. Magnetic Resonance Imaging. Melanoma / diagnosis. Papilloma, Inverted / diagnosis. Positron-Emission Tomography. Tomography, X-Ray Computed

  • MedlinePlus Health Information. consumer health - Nasal Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Copyright] Copyright (c) 2010 Mosby, Inc. All rights reserved.
  • (PMID = 20113866.001).
  • [ISSN] 1535-6302
  • [Journal-full-title] Current problems in diagnostic radiology
  • [ISO-abbreviation] Curr Probl Diagn Radiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


26. Pradhan B, Thapa N: Juvenile angiofibroma and its management. Nepal Med Coll J; 2009 Sep;11(3):186-8
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Juvenile angiofibroma and its management.
  • This prospective longitudinal study was done to determine extent of tumor and to highlight the importance of lateral rhinotomy approach for nasopharyngeal angiofibroma.
  • Patients with a diagnosis of nasopharyngeal angiofibroma who underwent surgery in Tribhuvan University Teaching Hospital, Maharajgunj, Kathmandu from April, 2004 to Jan 2009 were included in the study.
  • Two patients had stage I tumor, 9 patients had stage II disease, other 12 patients had stage III tumor.
  • Most of them had stage III disease and were managed surgically by lateral rhinotomy approach.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20334067.001).
  • [Journal-full-title] Nepal Medical College journal : NMCJ
  • [ISO-abbreviation] Nepal Med Coll J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Nepal
  •  go-up   go-down


27. Huang Y, Zhang L, Tian X, Qi B: [Surgery of nasopharyngeal angiofibroma]. Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2006 Mar;20(5):224-6
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Surgery of nasopharyngeal angiofibroma].
  • OBJECTIVE: To study the operations of nasopharyngeal angiofibroma.
  • METHOD: Twenty-two patients with nasopharyngeal angiofibroma operated by various operative approaches were studied in this research.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16722398.001).
  • [Journal-full-title] Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology
  • [ISO-abbreviation] Lin Chuang Er Bi Yan Hou Ke Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  •  go-up   go-down


28. Tang IP, Shashinder S, Gopala Krishnan G, Narayanan P: Juvenile nasopharyngeal angiofibroma in a tertiary centre: ten-year experience. Singapore Med J; 2009 Mar;50(3):261-4
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Juvenile nasopharyngeal angiofibroma in a tertiary centre: ten-year experience.
  • INTRODUCTION: This is a retrospective study that aimed to examine the outcomes of patients presenting with juvenile nasopharyngeal angiofibroma (JNA) at a tertiary centre in Malaysia.
  • One patient was at stage I, eight were at stage II, three at stage III and one patient was at stage IV, based on the Fisch classification.
  • CONCLUSION: JNA is a rare vascular benign tumour with highly exclusive persistence and recurrence, and typically affects adolescent boys.
  • [MeSH-major] Angiofibroma / diagnosis. Nasopharyngeal Neoplasms / diagnosis

  • Genetic Alliance. consumer health - TEN.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19352568.001).
  • [ISSN] 0037-5675
  • [Journal-full-title] Singapore medical journal
  • [ISO-abbreviation] Singapore Med J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Singapore
  •  go-up   go-down


29. La Placa M, Gibellini D, Bianchi T, Patrizi A: Overexpression of MLH-1 and psoriasin genes in cutaneous angiofibromas from tuberous sclerosis complex patients. J Cutan Pathol; 2006 Sep;33(9):608-13
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Overexpression of MLH-1 and psoriasin genes in cutaneous angiofibromas from tuberous sclerosis complex patients.
  • BACKGROUND: Tuberous sclerosis complex (TSC) is associated with mutations in two likely tumor-suppressor genes (TSC1 and TSC2) and characterized by the development of tumor-like growths (angiofibromas) in a variety of tissues and organs, particularly brain and skin.
  • RESULTS: The results obtained by the microarray technology in one hamartoma specimen, confirmed by the RT-PCR results obtained in the same material and in five other hamartoma specimens, demonstrated that TSC-related angiofibromas exhibit significant mRNA overexpression of two genes, represented by MLH-1 and psoriasin.
  • CONCLUSIONS: The overexpression of MLH-1, which codes for a DNA mismatch repair protein, and psoriasin, which codes for a specific chemoattractant factor for CD4+ T cells, implicated in the pathogenesis of inflammatory skin disease, and expressed in excess during abnormal pathways of cell growth, may shed light on the pathogenesis of the proliferative skin lesion.
  • [MeSH-major] Angiofibroma / genetics. Calcium-Binding Proteins / genetics. Carrier Proteins / genetics. Nuclear Proteins / genetics. Skin Neoplasms / genetics. Tuberous Sclerosis / genetics

  • Genetic Alliance. consumer health - Cutaneous Sclerosis.
  • Genetic Alliance. consumer health - Tuberous sclerosis.
  • MedlinePlus Health Information. consumer health - Skin Cancer.
  • MedlinePlus Health Information. consumer health - Tuberous Sclerosis.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16965334.001).
  • [ISSN] 0303-6987
  • [Journal-full-title] Journal of cutaneous pathology
  • [ISO-abbreviation] J. Cutan. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Denmark
  • [Chemical-registry-number] 0 / Adaptor Proteins, Signal Transducing; 0 / Biomarkers, Tumor; 0 / Calcium-Binding Proteins; 0 / Carrier Proteins; 0 / MLH1 protein, human; 0 / Nuclear Proteins; 0 / RNA, Messenger; 0 / S100 Proteins; 0 / S100A7 protein, human
  •  go-up   go-down


30. Li S, Takeuchi F, Wang JA, Fuller C, Pacheco-Rodriguez G, Moss J, Darling TN: MCP-1 overexpressed in tuberous sclerosis lesions acts as a paracrine factor for tumor development. J Exp Med; 2005 Sep 5;202(5):617-24
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Fibroblast-like cells from 10 angiofibromas and five periungual fibromas produced higher levels of monocyte chemoattractant protein-1 (MCP-1) mRNA and protein than did fibroblasts from the same patient's normal skin.
  • Conditioned medium from angiofibroma cells stimulated chemotaxis of a human monocytic cell line to a greater extent than conditioned medium from TSC fibroblasts, an effect blocked by neutralizing MCP-1-specific antibody.

  • Genetic Alliance. consumer health - Tuberous sclerosis.
  • MedlinePlus Health Information. consumer health - Tuberous Sclerosis.
  • COS Scholar Universe. author profiles.
  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .
  • NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .
  • The Lens. Cited by Patents in .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Tumori. 2003 Sep-Oct;89(5):459-68 [14870765.001]
  • [Cites] J Cutan Pathol. 2001 Oct;28(9):470-5 [11553313.001]
  • [Cites] J Am Soc Nephrol. 2004 Apr;15(4):940-8 [15034096.001]
  • [Cites] Expert Rev Cardiovasc Ther. 2003 Sep;1(3):393-400 [15030267.001]
  • [Cites] Am J Physiol Lung Cell Mol Physiol. 2004 May;286(5):L1038-44 [15064241.001]
  • [Cites] Cancer Cell. 2004 Jul;6(1):7-10 [15261137.001]
  • [Cites] J Cell Biol. 2004 Jul 19;166(2):213-23 [15249583.001]
  • [Cites] Am J Physiol Cell Physiol. 2004 Oct;287(4):C866-73 [15163622.001]
  • [Cites] Curr Biol. 2004 Sep 21;14(18):1650-6 [15380067.001]
  • [Cites] Arch Dermatol Res. 2001 Sep;293(9):460-9 [11758789.001]
  • [Cites] Hum Mol Genet. 2001 Dec 1;10(25):2899-905 [11741833.001]
  • [Cites] J Am Acad Dermatol. 2002 Mar;46(3):376-80 [11862172.001]
  • [Cites] Transplantation. 2002 Mar 27;73(6):915-20 [11923692.001]
  • [Cites] Int J Oncol. 2003 Apr;22(4):773-8 [12632067.001]
  • [Cites] J Cutan Pathol. 2003 Mar;30(3):174-7 [12641776.001]
  • [Cites] J Leukoc Biol. 2003 May;73(5):639-49 [12714579.001]
  • [Cites] Cancer Res. 2003 May 15;63(10):2675-80 [12750296.001]
  • [Cites] Biochem Soc Trans. 2003 Jun;31(Pt 3):592-6 [12773162.001]
  • [Cites] Proc Natl Acad Sci U S A. 2003 Jun 10;100(12):7265-70 [12756299.001]
  • [Cites] Clin Exp Rheumatol. 2003 May-Jun;21(3):369-75 [12846061.001]
  • [Cites] Lab Invest. 2003 Jul;83(7):927-38 [12861033.001]
  • [Cites] J Invest Dermatol. 2003 Sep;121(3):510-6 [12925209.001]
  • [Cites] Cancer Cell. 2003 Aug;4(2):147-58 [12957289.001]
  • [Cites] Cancer Res. 2003 Sep 1;63(17):5173-7 [14500340.001]
  • [Cites] Neurobiol Dis. 2003 Nov;14(2):279-90 [14572449.001]
  • [Cites] Atherosclerosis. 2004 Jan;172(1):31-8 [14709354.001]
  • [Cites] Trends Biochem Sci. 2004 Jan;29(1):32-8 [14729330.001]
  • [Cites] J Cutan Pathol. 1989 Oct;16(5):266-71 [2574200.001]
  • [Cites] J Dermatol. 1989 Aug;16(4):263-9 [2600265.001]
  • [Cites] J Dermatol Sci. 1991 Jan;2(1):50-4 [1675869.001]
  • [Cites] Neuropathol Appl Neurobiol. 1992 Dec;18(6):559-65 [1283203.001]
  • [Cites] J Invest Dermatol. 1995 Nov;105(5):635-43 [7594634.001]
  • [Cites] Br J Dermatol. 1996 Jul;135(1):1-5 [8776349.001]
  • [Cites] Pediatr Pathol Lab Med. 1996 Nov-Dec;16(6):893-9 [9025887.001]
  • [Cites] Proc Natl Acad Sci U S A. 1998 Dec 22;95(26):15653-8 [9861025.001]
  • [Cites] J Child Neurol. 1998 Dec;13(12):624-8 [9881533.001]
  • [Cites] J Biol Chem. 2005 Feb 18;280(7):5870-4 [15576369.001]
  • [Cites] Blood. 2000 Jul 1;96(1):34-40 [10891427.001]
  • [Cites] Transplantation. 2001 Apr 27;71(8):1179-83 [11374423.001]
  • [Cites] Am J Hum Genet. 2001 Sep;69(3):493-503 [11468687.001]
  • [Cites] J Investig Med. 2001 Sep;49(5):421-33 [11523698.001]
  • [Cites] J Cutan Pathol. 2004 Mar;31(3):241-6 [14984576.001]
  • (PMID = 16129702.001).
  • [ISSN] 0022-1007
  • [Journal-full-title] The Journal of experimental medicine
  • [ISO-abbreviation] J. Exp. Med.
  • [Language] ENG
  • [Grant] United States / NCI NIH HHS / CA / R01 CA100907; United States / NCI NIH HHS / CA / 1 R01 CA100907
  • [Publication-type] Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S.
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antibodies; 0 / CCL2 protein, human; 0 / Chemokine CCL2; 0 / Culture Media, Conditioned; 0 / Tumor Suppressor Proteins; 4JG2LF96VF / tuberous sclerosis complex 2 protein
  • [Other-IDs] NLM/ NIHMS7508; NLM/ PMC1378109
  •  go-up   go-down


31. Tyagi I, Syal R, Goyal A: Staging and surgical approaches in large juvenile angiofibroma--study of 95 cases. Int J Pediatr Otorhinolaryngol; 2006 Sep;70(9):1619-27
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Staging and surgical approaches in large juvenile angiofibroma--study of 95 cases.
  • INTRODUCTION: Surgery has been the treatment of choice for juvenile nasopharyngeal angiofibroma (JNA) and selection of proper surgical approach depends primarily upon the extensions of the tumor.
  • Lazy S incision was used and combined transmaxillary and transpalatal removal of angiofibroma was done in most of the cases.
  • [MeSH-major] Angiofibroma / pathology. Angiofibroma / surgery. Nasopharyngeal Neoplasms / pathology. Nasopharyngeal Neoplasms / surgery

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16777240.001).
  • [ISSN] 0165-5876
  • [Journal-full-title] International journal of pediatric otorhinolaryngology
  • [ISO-abbreviation] Int. J. Pediatr. Otorhinolaryngol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Ireland
  •  go-up   go-down


32. Hofbauer GF, Marcollo-Pini A, Corsenca A, Kistler AD, French LE, Wüthrich RP, Serra AL: The mTOR inhibitor rapamycin significantly improves facial angiofibroma lesions in a patient with tuberous sclerosis. Br J Dermatol; 2008 Aug;159(2):473-5
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] The mTOR inhibitor rapamycin significantly improves facial angiofibroma lesions in a patient with tuberous sclerosis.
  • Tuberous sclerosis complex (TSC) is an autosomal dominant disorder with an incidence of approximately one in 6000.
  • It arises from a genetic abnormality involving either the TSC1 gene on chromosome 9 or the TSC2 gene on chromosome 16.
  • Angiofibroma affects 70-80% of patients with TSC, typically on the face.
  • Immunosuppressive treatment with rapamycin, a specific mTOR inhibitor, initiated because of renal transplantation, reduced facial angiofibroma dramatically.
  • [MeSH-major] Angiofibroma / drug therapy. Facial Neoplasms / drug therapy. Sirolimus / therapeutic use. Skin Neoplasms / drug therapy. Tuberous Sclerosis / complications


33. Nzegwu MA, Uguru C, Okafor OC, Ifeoma O, Olusina D: Patterns of oral and jaw tumours seen in eastern Nigeria: a review of sixty cases seen over a 5-year period--1 January 2000 to 31 December 2004. Eur J Cancer Care (Engl); 2008 Nov;17(6):532-4
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Sixty oral and jaw tumours were received out of a total of 4500 specimens constituting 1.3% of all biopsies.
  • The categories were calcifying odontogenic cysts and fibromas 11 (18.3%).
  • Fibrous dysplasia seven (11.7%).
  • Butyroid rhabdomyosarcoma, adenoid cystic carcinoma angiofibroma, fibrous histiocytoma and fibrosarcoma were each one (1.7%).
  • The most common subtype seen were the dentigerous cysts/fibromas, followed by ameloblastomas.

  • MedlinePlus Health Information. consumer health - Oral Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18754768.001).
  • [ISSN] 1365-2354
  • [Journal-full-title] European journal of cancer care
  • [ISO-abbreviation] Eur J Cancer Care (Engl)
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] England
  •  go-up   go-down


34. Qian YW, Malliah R, Lee HJ, Das K, Mirani N, Hameed M: A t(12;17) in an extraorbital giant cell angiofibroma. Cancer Genet Cytogenet; 2006 Mar;165(2):157-60
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A t(12;17) in an extraorbital giant cell angiofibroma.
  • We report a case of a 43-year-old male who presented with a large soft-tissue neck mass 7 years ago.
  • A diagnosis of giant cell angiofibroma (GCA) was made on the basis of light microscopy and immunohistochemical studies.
  • This cytogenetic abnormality in GCA is different from the t(17;22)(q22;q13) found in related lesions, such as giant cell fibroblastoma and solitary fibrous tumor, none of which has a specific chromosomal abnormality.
  • [MeSH-major] Angiofibroma / genetics. Chromosomes, Human, Pair 12. Chromosomes, Human, Pair 17. Head and Neck Neoplasms / genetics. Translocation, Genetic

  • MedlinePlus Health Information. consumer health - Head and Neck Cancer.
  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Copyright] 2006 Elsevier Inc. All rights reserved.
  • (PMID = 16527610.001).
  • [ISSN] 0165-4608
  • [Journal-full-title] Cancer genetics and cytogenetics
  • [ISO-abbreviation] Cancer Genet. Cytogenet.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


35. Koo PJ, Goykhman I, Lembert L, Nunes LW: MRI features of cellular angiomyofibroma with pathologic correlation. J Magn Reson Imaging; 2009 May;29(5):1195-8
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Within the spectrum of extratesticular mesenchymal tumors in the scrotum and perineum lies cellular angiofibroma, also known as angiomyofibroblastoma-like tumor, a rare lesion originally described to almost exclusively occur in the vulva, perineum, and pelvis of women.
  • We present the MRI features of cellular angiofibroma that are consistent with the pathological characteristics of this entity-a benign cellular and fibrous tumor with prominent vascularity.

  • MedlinePlus Health Information. consumer health - MRI Scans.
  • MedlinePlus Health Information. consumer health - Testicular Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19388110.001).
  • [ISSN] 1053-1807
  • [Journal-full-title] Journal of magnetic resonance imaging : JMRI
  • [ISO-abbreviation] J Magn Reson Imaging
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


36. Onerci M, Oğretmenoğlu O, Yücel T: Juvenile nasopharyngeal angiofibroma: a revised staging system. Rhinology; 2006 Mar;44(1):39-45
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Juvenile nasopharyngeal angiofibroma: a revised staging system.
  • METHODS: The medical records of 36 patients, all of whom underwent resection of juvenile nasopharyngeal angiofibroma by external or endonasal approach between 1983 and 2002, were reviewed retrospectively.
  • Tumour extent, sites and rate of persistent disease were analyzed and compared with the literature.
  • RESULTS: Persistent or recurrent disease was found in 12 of the 36 patients (33%).
  • Involvement of the pterygoid process base was observed in only 3 of the 24 patients without persistent disease, whereas it was found 10 out of 12 patients with persistent disease.
  • CONCLUSIONS: Advances in radiographic imaging, embolization, and surgical methods of treating angiofibromas have changed the sites associated with a high risk for persistent disease or morbidity.
  • In the light of all these recent advances, data from our series, and the literature, we suggested a new classification for determining the risk of persistent disease, choosing the appropriate surgical method, and for maintaining uniformity.
  • [MeSH-minor] Adolescent. Angiofibroma. Humans. Magnetic Resonance Imaging. Male. Neoplasm Invasiveness. Neoplasm Recurrence, Local. Neoplasm Staging. Neoplasm, Residual. Paranasal Sinus Neoplasms / pathology. Paranasal Sinus Neoplasms / radiography. Paranasal Sinus Neoplasms / surgery. Tomography, X-Ray Computed

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16550949.001).
  • [ISSN] 0300-0729
  • [Journal-full-title] Rhinology
  • [ISO-abbreviation] Rhinology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
  •  go-up   go-down


37. Coutinho-Camillo CM, Brentani MM, Nagai MA: Genetic alterations in juvenile nasopharyngeal angiofibromas. Head Neck; 2008 Mar;30(3):390-400
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Genetic alterations in juvenile nasopharyngeal angiofibromas.
  • Juvenile nasopharyngeal angiofibroma (JNA) is a rare benign neoplasm of the nasopharynx that accounts for 0.5% of all head and neck tumors.
  • Although histologically benign in appearance, JNAs are locally aggressive and destructive, spreading from the nasal cavity to the nasopharynx, paranasal sinuses, and orbit skull base with intracranial extension.
  • [MeSH-major] Angiofibroma / genetics. Nasopharyngeal Neoplasms / genetics

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Copyright] (c) 2008 Wiley Periodicals, Inc. Head Neck, 2008.
  • (PMID = 18228521.001).
  • [ISSN] 1043-3074
  • [Journal-full-title] Head & neck
  • [ISO-abbreviation] Head Neck
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Intercellular Signaling Peptides and Proteins; 0 / RNA, Messenger; 0 / Receptors, Steroid; 0 / beta Catenin; EC 2.5.1.18 / Glutathione Transferase
  • [Number-of-references] 103
  •  go-up   go-down


38. Wosnitzer B, Gadiraju R: The role of nuclear imaging in multiple endocrine neoplasia 1 (MEN 1). Radiol Case Rep; 2010;5(4):452
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Multiple endocrine neoplasia 1 (MEN 1) is a rare genetic disorder classically characterized by a predisposition to tumors of the parathyroid glands, anterior pituitary gland, and pancreatic islet cells (1).
  • In addition to exhibiting these characteristic tumors, MEN 1 patients also have an increased propensity for other tumors such as carcinoids, adrenal adenomas, angiofibromas, and lipomas (1, 2, 3).
  • The tumors of MEN 1 are usually benign; however, malignancy of some carcinoid, islet cell, and gastrointestinal tract tumors can cause mortality (5, 6, 7, 8).

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 27307880.001).
  • [ISSN] 1930-0433
  • [Journal-full-title] Radiology case reports
  • [ISO-abbreviation] Radiol Case Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
  • [Other-IDs] NLM/ PMC4901017
  • [Keywords] NOTNLM ; CT, computed tomography / EGD, esophagogastroduodenoscopy / MEN 1, multiple endocrine neoplasia 1 / MRI, magnetic resonance imaging
  •  go-up   go-down


39. Scott MT, Roper M, Mura J: Vertebral artery reconstruction using microanastomosis and intraoperative neuromonitoring: a case report from Santiago, Chile. Am J Electroneurodiagnostic Technol; 2008 Jun;48(2):79-92
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The preliminary result of the biopsy was an angiofibroma.

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18680896.001).
  • [ISSN] 1086-508X
  • [Journal-full-title] American journal of electroneurodiagnostic technology
  • [ISO-abbreviation] Am J Electroneurodiagnostic Technol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


40. Pamir MN, Kilic T, Ozek MM, Ozduman K, Türe U: Non-meningeal tumours of the cavernous sinus: a surgical analysis. J Clin Neurosci; 2006 Jul;13(6):626-35
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • A retrospective analysis of 42 cases of benign non-meningeal tumours of the cavernous sinus operated on at Marmara University between April 1992 and April 2003 is presented.
  • The study cohort consisted of 13 pituitary adenomas, 11 trigeminal schwannomas, seven chordomas, three chondrosarcomas, two juvenile angiofibromas, two epidermoid tumours, one plasmacytoma, one cavernous haemangioma and one internal carotid plexus schwannoma.

  • MedlinePlus Health Information. consumer health - Brain Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16860718.001).
  • [ISSN] 0967-5868
  • [Journal-full-title] Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
  • [ISO-abbreviation] J Clin Neurosci
  • [Language] eng
  • [Publication-type] Clinical Trial; Comparative Study; Journal Article
  • [Publication-country] Scotland
  •  go-up   go-down


41. Cole RP, Widdowson D, Moore JC: Outcome of erbium:yttrium aluminium garnet laser resurfacing treatments. Lasers Med Sci; 2008 Oct;23(4):427-33
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Erbium:yttrium aluminium garnet (erbium:YAG) laser treatment was used to resurface skin abnormalities in patients suffering from conditions that included epidermal naevi, tuberous sclerosis, angiofibromata, neurofibromatosis, and scarring caused by acne or other means.
  • [MeSH-major] Laser Therapy / instrumentation. Lasers, Solid-State. Skin Diseases / surgery

  • MedlinePlus Health Information. consumer health - Skin Conditions.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Br J Plast Surg. 1996 Oct;49(7):433-8 [8983542.001]
  • [Cites] Chest. 1997 Nov 5;112(5):1165-74 [9367452.001]
  • [Cites] J Consult Clin Psychol. 1969 Aug;33(4):448-57 [5810590.001]
  • [Cites] Clin Exp Dermatol. 2004 Sep;29(5):494-6 [15347334.001]
  • [Cites] Br J Plast Surg. 1997 Jun;50(4):242-8 [9215080.001]
  • [Cites] Aesthetic Plast Surg. 2003 Mar-Apr;27(2):130-4 [14629067.001]
  • [Cites] Med Care. 1992 Jun;30(6):473-83 [1593914.001]
  • [Cites] Br J Psychol. 1955 May;46(2):130-8 [14378538.001]
  • [Cites] Br J Plast Surg. 1994 Mar;47(2):117-21 [8149054.001]
  • [Cites] Acta Psychiatr Scand. 1983 Jun;67(6):361-70 [6880820.001]
  • [Cites] Plast Reconstr Surg. 2002 Jan;109(1):363-9; discussion 370-1 [11786842.001]
  • [Cites] J Otolaryngol. 2000 Dec;29(6):377-81 [11770147.001]
  • [Cites] Ann Plast Surg. 1997 Feb;38(2):95-100 [9043576.001]
  • [Cites] J Plast Reconstr Aesthet Surg. 2006;59(1):65-73 [16482791.001]
  • [Cites] Lasers Surg Med. 1997;20(3):242-7 [9138252.001]
  • [Cites] Plast Reconstr Surg. 2003 Aug;112(2):619-25; discussion 626-7 [12900625.001]
  • [Cites] Arch Dermatol. 2003 Oct;139(10):1295-9 [14568834.001]
  • [Cites] J Plast Reconstr Aesthet Surg. 2006;59(1):54-64 [16482790.001]
  • (PMID = 18074165.001).
  • [ISSN] 0268-8921
  • [Journal-full-title] Lasers in medical science
  • [ISO-abbreviation] Lasers Med Sci
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  •  go-up   go-down


42. Micheletti AM, Silva AC, Nascimento AG, Da Silva CS, Murta EF, Adad SJ: Cellular angiofibroma of the vulva: case report with clinicopathological and immunohistochemistry study. Sao Paulo Med J; 2005 Sep 1;123(5):250-2
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cellular angiofibroma of the vulva: case report with clinicopathological and immunohistochemistry study.
  • CONTEXT: Cellular angiofibroma of the vulva is a rare tumor that was first described in 1997.
  • The differential diagnoses for this tumor include aggressive angiomyxoma, angiomyofibroblastoma, lipoma of fusiform cells, solitary fibrous tumor, perineurioma and leiomyoma.
  • [MeSH-major] Angiofibroma / diagnosis. Bartholin's Glands. Cysts / diagnosis. Vulvar Neoplasms / diagnosis

  • MedlinePlus Health Information. consumer health - Vulvar Cancer.
  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16358102.001).
  • [ISSN] 1516-3180
  • [Journal-full-title] São Paulo medical journal = Revista paulista de medicina
  • [ISO-abbreviation] Sao Paulo Med J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Brazil
  •  go-up   go-down


43. Korcum AF, Ağirdir BV, Aksu G, Güney K, Dinç O: [Treatment modalities of nasopharyngeal angiofibroma]. Kulak Burun Bogaz Ihtis Derg; 2008 Jul-Aug;18(4):263-7
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Treatment modalities of nasopharyngeal angiofibroma].
  • Nasopharyngeal angiofibroma is a rare, benign vascular tumor originating from the sphenopalatine foramen.
  • Many treatment modalities have been used for the management of nasopharyngeal angiofibroma, but surgery and external beam radiation therapy have proved to be the only effective treatment modalities with acceptable morbidity.
  • [MeSH-major] Angiofibroma / radiotherapy. Angiofibroma / surgery. Nasopharyngeal Neoplasms / radiotherapy. Nasopharyngeal Neoplasms / surgery

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19052499.001).
  • [ISSN] 1300-7475
  • [Journal-full-title] Kulak burun boğaz ihtisas dergisi : KBB = Journal of ear, nose, and throat
  • [ISO-abbreviation] Kulak Burun Bogaz Ihtis Derg
  • [Language] tur
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Turkey
  • [Number-of-references] 39
  •  go-up   go-down


44. Zhou SH, Wang SQ, Wang QY: [Atypical angiofibroma in inferior nasal turbinate: report of a case]. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2008 Jan;43(1):68
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Atypical angiofibroma in inferior nasal turbinate: report of a case].
  • [MeSH-major] Angiofibroma. Nose Diseases. Turbinates / pathology

  • MedlinePlus Health Information. consumer health - Nose Injuries and Disorders.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18357720.001).
  • [ISSN] 1673-0860
  • [Journal-full-title] Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
  • [ISO-abbreviation] Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
  • [Language] chi
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] China
  •  go-up   go-down


45. Schwartz RA, Fernández G, Kotulska K, Jóźwiak S: Tuberous sclerosis complex: advances in diagnosis, genetics, and management. J Am Acad Dermatol; 2007 Aug;57(2):189-202
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The classic triad is seizures, mental retardation, and cutaneous angiofibromas.
  • [MeSH-minor] Diagnosis, Differential. Humans. Molecular Diagnostic Techniques. Mutation. Protein Kinases / drug effects. Protein Kinases / metabolism. Sirolimus / therapeutic use. Skin Diseases / etiology. Skin Diseases / pathology. TOR Serine-Threonine Kinases. Tooth Diseases / etiology. Tooth Diseases / pathology


46. Ramezani A, Haghighatkhah H, Moghadasi H, Taheri MS, Parsafar H: A case of central retinal artery occlusion following embolization procedure for juvenile nasopharyngeal angiofibroma. Indian J Ophthalmol; 2010 Sep-Oct;58(5):419-21
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A case of central retinal artery occlusion following embolization procedure for juvenile nasopharyngeal angiofibroma.
  • A 23-year-old male patient with right nasal Juvenile Nasopharyngeal Angiofibroma (JNA) developed Central Retinal Artery Occlusion (CRAO) during embolization of the tumor using polyvinyl alcohol particles before endoscopic excision.
  • [MeSH-major] Angiofibroma / therapy. Embolization, Therapeutic / adverse effects. Nasopharyngeal Neoplasms / therapy. Retinal Artery Occlusion / etiology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Ophthalmology. 1980 Jan;87(1):75-8 [6769079.001]
  • [Cites] Ophthalmology. 1995 Dec;102(12):2029-34; discussion 2034-5 [9098313.001]
  • [Cites] Curr Opin Otolaryngol Head Neck Surg. 2006 Feb;14(1):1-5 [16467630.001]
  • [Cites] J Laryngol Otol. 1999 Feb;113(2):127-34 [10396561.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 2005 Mar;69(3):423-8 [15733605.001]
  • [Cites] AJNR Am J Neuroradiol. 1999 Jan;20(1):179-81 [9974079.001]
  • (PMID = 20689199.001).
  • [ISSN] 1998-3689
  • [Journal-full-title] Indian journal of ophthalmology
  • [ISO-abbreviation] Indian J Ophthalmol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC2992919
  •  go-up   go-down


47. Zeller S, Marx SJ, Lungu AO, Cowen EW, Turner ML: Multiple angiofibromas and collagenomas in a 45-year-old man with recurrent nephrolithiasis, fatigue, and vision loss. J Am Acad Dermatol; 2009 Aug;61(2):319-22
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Multiple angiofibromas and collagenomas in a 45-year-old man with recurrent nephrolithiasis, fatigue, and vision loss.
  • [MeSH-major] Angiofibroma / diagnosis. Multiple Endocrine Neoplasia Type 1 / diagnosis. Skin Neoplasms / diagnosis
  • [MeSH-minor] Adrenalectomy / methods. Biopsy, Needle. Collagen Diseases / complications. Collagen Diseases / diagnosis. Fatigue / complications. Fatigue / diagnosis. Follow-Up Studies. Humans. Immunohistochemistry. Male. Middle Aged. Nephrolithiasis / complications. Nephrolithiasis / diagnosis. Pancreatectomy. Recurrence. Risk Assessment. Severity of Illness Index. Splenectomy / methods. Vision Disorders / complications. Vision Disorders / diagnosis

  • MedlinePlus Health Information. consumer health - Skin Cancer.
  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Hum Mutat. 2008 Jan;29(1):22-32 [17879353.001]
  • [Cites] Clin Endocrinol (Oxf). 2009 Apr;70(4):575-81 [18616711.001]
  • [Cites] Endocr J. 2000 Oct;47(5):569-73 [11200937.001]
  • [Cites] Trends Endocrinol Metab. 2001 May-Jun;12(4):173-8 [11295574.001]
  • [Cites] J Clin Endocrinol Metab. 2001 Dec;86(12):5658-71 [11739416.001]
  • [Cites] J Clin Endocrinol Metab. 2002 Feb;87(2):457-65 [11836268.001]
  • [Cites] J Clin Endocrinol Metab. 2004 Nov;89(11):5328-36 [15531478.001]
  • [Cites] Arch Dermatol. 1997 Jul;133(7):853-7 [9236523.001]
  • [Cites] J Invest Dermatol. 1998 Apr;110(4):438-40 [9540988.001]
  • [Cites] J Clin Endocrinol Metab. 1998 Aug;83(8):2617-20 [9709920.001]
  • [Cites] J Invest Dermatol. 1998 Sep;111(3):539-40 [9740255.001]
  • [Cites] J Clin Oncol. 1999 Feb;17(2):615-30 [10080607.001]
  • [Cites] Science. 1997 Apr 18;276(5311):404-7 [9103196.001]
  • (PMID = 19615541.001).
  • [ISSN] 1097-6787
  • [Journal-full-title] Journal of the American Academy of Dermatology
  • [ISO-abbreviation] J. Am. Acad. Dermatol.
  • [Language] eng
  • [Grant] United States / Intramural NIH HHS / / Z99 CA999999
  • [Publication-type] Case Reports; Journal Article; Research Support, N.I.H., Intramural
  • [Publication-country] United States
  • [Other-IDs] NLM/ NIHMS135687; NLM/ PMC2744374
  •  go-up   go-down


48. Korol UB, Schoor R, Nanda V, Almas K, Phelan JA: Gingival enlargement as a manifestation of tuberous sclerosis: case report and periodontal management. J Periodontol; 2008 Apr;79(4):759-63
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Tuberous sclerosis is an autosomal-dominant inherited disease involving many organs of the body.
  • Oral manifestations include gingival enlargement, fibromas, and dental enamel pitting.
  • The report presents a case of tuberous sclerosis with gingival enlargement histologically consistent with angiofibroma, describes its successful periodontal management, and reviews the literature associated with oral manifestations of tuberous sclerosis.
  • RESULTS: Histologic examination of the gingival tissue revealed features consistent with angiofibroma.
  • CONCLUSIONS: The gingival enlargement was histologically consistent with the characteristic angiofibromas of tuberous sclerosis.
  • [MeSH-minor] Adult. Angiofibroma / pathology. Debridement. Dental Scaling. Follow-Up Studies. Gingival Neoplasms / pathology. Gingivectomy. Humans. Male. Toothbrushing

  • Genetic Alliance. consumer health - Tuberous sclerosis.
  • MedlinePlus Health Information. consumer health - Tuberous Sclerosis.
  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18380572.001).
  • [ISSN] 0022-3492
  • [Journal-full-title] Journal of periodontology
  • [ISO-abbreviation] J. Periodontol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 30
  •  go-up   go-down


49. Celenk P, Alkan A, Canger EM, Günhan O: Fibrolipomatous hamartoma in a patient with tuberous sclerosis: report of a case. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2005 Feb;99(2):202-6
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Fibrolipomatous hamartoma in a patient with tuberous sclerosis: report of a case.
  • Tuberous sclerosis is a rare congenital disorder with an incidence of 1 in 6000 births.
  • The classic triad is seizure, mental deficiency, and angiofibromas.
  • Orofacial manifestations include fibrous hyperplasia, hemangioma, bifid uvula, cleft lip and palate, macroglossia, high arched palate, and enamel defects.
  • Benign tumors of the jaws including desmoplastic fibroma, calcifying odontogenic tumor, and odontogenic myxoma have been recently reported in tuberous sclerosis.
  • [MeSH-major] Hamartoma / complications. Mandibular Diseases / complications. Tuberous Sclerosis / complications

  • Genetic Alliance. consumer health - Tuberous sclerosis.
  • MedlinePlus Health Information. consumer health - Tuberous Sclerosis.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15660093.001).
  • [ISSN] 1079-2104
  • [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; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 9007-34-5 / Collagen
  •  go-up   go-down


50. Hodges JM, McDevitt AS, El-Sayed Ali AI, Sebelik ME: Juvenile nasopharyngeal angiofibroma: current treatment modalities and future considerations. Indian J Otolaryngol Head Neck Surg; 2010 Sep;62(3):236-47
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Juvenile nasopharyngeal angiofibroma: current treatment modalities and future considerations.
  • Juvenile angiofibroma (JNA) is a relatively uncommon, highly vascular and benign tumor that presents most commonly in adolescent males.
  • With the advent of more sophisticated capabilities such as CT, MRI, intensity-modulated radiation therapy (IMRT), stereotactic guidance systems as well as advanced embolization techniques, these tumors can be diagnosed and managed more effectively.Patients with juvenile angiofibroma (JNA) are typically silent for years and often present with epistaxis, nasal obstruction, facial numbness, rhinorrhea, ear popping, sinusitis, cheek swelling, visual changes and headaches.
  • In addition to these symptoms, up to one-third of patients with this condition may present with proptosis or other orbital involvement, which are late symptoms and findings.Most physicians agree that surgery is the primary treatment modality for the early-stage disease process.
  • However, controversy arises regarding the best treatment when a patient presents with more locally advanced disease involving widespread cranial-based extension or intracranial involvement which may necessitate a combination of treatment modalities including surgery and postoperative radiation.With the advancement of endoscopic surgery, there have been a number of cases reporting the value of its use.

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Rhinology. 2003 Dec;41(4):235-40 [14750351.001]
  • [Cites] Laryngoscope. 2004 Feb;114(2):291-3 [14755205.001]
  • [Cites] J Craniomaxillofac Surg. 2006 Jan;34(1):3-8 [16343920.001]
  • [Cites] Rhinology. 2006 Mar;44(1):39-45 [16550949.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 2006 Sep;70(9):1619-27 [16777240.001]
  • [Cites] Rhinology. 2007 Mar;45(1):24-30 [17432065.001]
  • [Cites] Otolaryngol Head Neck Surg. 2007 Sep;137(3):492-6 [17765782.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 2008 Jun;72(6):793-800 [18387676.001]
  • [Cites] Otolaryngol Head Neck Surg. 2008 Jul;139(1):168-9 [18585585.001]
  • [Cites] Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009 Feb;107(2):180-4 [18926733.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 2009 Mar;73(3):401-8 [19124161.001]
  • [Cites] Am J Otolaryngol. 2010 Sep-Oct;31(5):343-9 [20015778.001]
  • [Cites] Plast Reconstr Surg. 1987 Oct;80(4):491-9 [3659159.001]
  • [Cites] Ann Otol Rhinol Laryngol. 1984 Jul-Aug;93(4 Pt 1):322-9 [6087710.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 1993 Dec;28(1):51-61 [8300314.001]
  • [Cites] J Cardiothorac Vasc Anesth. 2003 Oct;17(5):622-4 [14579217.001]
  • [Cites] Arch Otolaryngol Head Neck Surg. 2007 Dec;133(12):1209-14 [18086961.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 2009 May;73(5):689-92 [19230984.001]
  • [Cites] Laryngoscope. 1978 Aug;88(8 Pt 1):1247-51 [209265.001]
  • [Cites] Plast Reconstr Surg. 1991 Sep;88(3):395-403 [1871215.001]
  • [Cites] Plast Reconstr Surg. 1991 Feb;87(2):229-35 [1989014.001]
  • [Cites] Laryngoscope. 1989 Apr;99(4):429-37 [2538688.001]
  • [Cites] Acta Otolaryngol. 1988 Jan-Feb;105(1-2):132-9 [2829500.001]
  • [Cites] Laryngoscope. 1984 Dec;94(12 Pt 1):1599-605 [6094932.001]
  • [Cites] J Otolaryngol. 1984 Dec;13(6):391-4 [6100552.001]
  • [Cites] Head Neck Surg. 1981 Mar-Apr;3(4):279-83 [6260711.001]
  • [Cites] Clin Plast Surg. 1982 Oct;9(4):445-56 [6756757.001]
  • [Cites] Arch Otolaryngol Head Neck Surg. 1996 Feb;122(2):122-9 [8630204.001]
  • [Cites] J Formos Med Assoc. 1998 Dec;97(12):845-9 [9884487.001]
  • [Cites] J Laryngol Otol. 1999 Feb;113(2):127-34 [10396561.001]
  • [Cites] J Otolaryngol. 1999 Jun;28(3):145-51 [10410346.001]
  • [Cites] Laryngoscope. 2001 Apr;111(4 Pt 1):681-7 [11359140.001]
  • [Cites] Laryngoscope. 2001 Sep;111(9):1509-11 [11568597.001]
  • [Cites] Arch Otolaryngol Head Neck Surg. 2002 Aug;128(8):928-35 [12162773.001]
  • [Cites] Arch Otolaryngol Head Neck Surg. 2002 Sep;128(9):1071-8 [12220215.001]
  • [Cites] Am J Otolaryngol. 2002 Sep-Oct;23(5):282-6 [12239693.001]
  • [Cites] Auris Nasus Larynx. 2002 Oct;29(4):395-400 [12393050.001]
  • [Cites] Neurol Med Chir (Tokyo). 2002 Oct;42(10):439-42 [12416568.001]
  • [Cites] Clin Otolaryngol Allied Sci. 2002 Dec;27(6):536-40 [12472527.001]
  • [Cites] Neurosurgery. 2003 May;52(5):1207-11; discussion 1211 [12699567.001]
  • [Cites] Arch Otolaryngol Head Neck Surg. 2003 Apr;129(4):454-9 [12707194.001]
  • [Cites] Laryngoscope. 2003 May;113(5):775-82 [12792310.001]
  • [Cites] Otolaryngol Head Neck Surg. 2003 Dec;129(6):684-91 [14663436.001]
  • (PMID = 23120720.001).
  • [ISSN] 2231-3796
  • [Journal-full-title] Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India
  • [ISO-abbreviation] Indian J Otolaryngol Head Neck Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC3450247
  • [Keywords] NOTNLM ; Angiofibroma / Cyberknife / Embolization / Endoscopic surgery / IMRT / Image guided robotic radiotherapy / Skull base / Vascular tumor
  •  go-up   go-down


51. Mohindra S, Grover G, Bal AK: Extranasopharyngeal angiofibroma of the nasal septum: a case report. Ear Nose Throat J; 2009 Nov;88(11):E17-9
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Extranasopharyngeal angiofibroma of the nasal septum: a case report.
  • Angiofibroma arising outside the nasopharynx is unusual.
  • The nasal septum is an extremely rare site for the origin of angiofibroma, and to date only 6 such cases previously have been reported in the literature.
  • We report here a case of a 22-year-old man with a vascular mass arising from his nasal septum.
  • The histopathology report was consistent with angiofibroma.
  • We also review other cases in the literature of angiofibroma arising from the nasal septum and discuss a theory of the likely origin of angiofibroma.
  • [MeSH-major] Angiofibroma / diagnosis. Nasal Septum / pathology. Nasopharyngeal Neoplasms / diagnosis. Nose Neoplasms / diagnosis

  • MedlinePlus Health Information. consumer health - Nasal Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19924651.001).
  • [ISSN] 1942-7522
  • [Journal-full-title] Ear, nose, & throat journal
  • [ISO-abbreviation] Ear Nose Throat J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 12
  •  go-up   go-down


52. Schick B, Veldung B, Wemmert S, Jung V, Montenarh M, Meese E, Urbschat S: p53 and Her-2/neu in juvenile angiofibromas. Oncol Rep; 2005 Mar;13(3):453-7
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] p53 and Her-2/neu in juvenile angiofibromas.
  • The pathogenesis of juvenile angiofibroma (JA) remains unsolved.
  • [MeSH-major] Angiofibroma / genetics. Angiofibroma / physiopathology. Chromosomes, Human, Pair 17. Gene Expression Profiling. Receptor, ErbB-2 / biosynthesis. Tumor Suppressor Protein p53 / biosynthesis

  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15706416.001).
  • [ISSN] 1021-335X
  • [Journal-full-title] Oncology reports
  • [ISO-abbreviation] Oncol. Rep.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Greece
  • [Chemical-registry-number] 0 / RNA, Messenger; 0 / Tumor Suppressor Protein p53; EC 2.7.10.1 / Receptor, ErbB-2
  •  go-up   go-down


53. Gengler C, Guillou L: Solitary fibrous tumour and haemangiopericytoma: evolution of a concept. Histopathology; 2006 Jan;48(1):63-74
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Solitary fibrous tumour and haemangiopericytoma: evolution of a concept.
  • Over the years, it appeared that this growth pattern was a non-specific one, shared by numerous, unrelated benign and malignant lesions, and that HPC was better considered as a diagnosis of exclusion.
  • They generally show a benign clinical course, and include glomangiopericytoma/myopericytoma, infantile myofibromatosis (previously called infantile HPC), and a subset of sinonasal HPCs.
  • The third category is the solitary fibrous tumour (SFT) lesional group, which includes fibrous-to-cellular SFTs, and related lesions such as giant cell angiofibromas and lipomatous HPCs.
  • [MeSH-major] Fibroma / diagnosis. Hemangiopericytoma / diagnosis. Soft Tissue Neoplasms / diagnosis

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16359538.001).
  • [ISSN] 0309-0167
  • [Journal-full-title] Histopathology
  • [ISO-abbreviation] Histopathology
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 70
  •  go-up   go-down


54. Satish Chandra A, Mohanty S: Subselective embolisation in management of JNA. Indian J Otolaryngol Head Neck Surg; 2007 Mar;59(1):43-4
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Role of Embolisation in preoperative management of Nasopharyngeal angiofibroma is well established in present day therapeutic modalities.

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Radiology. 1979 Sep;132(3):631-9 [472240.001]
  • [Cites] J Neuroradiol. 1979;6(1):45-53 [479928.001]
  • [Cites] Laryngoscope. 1987 Nov;97(11):1319-25 [2823033.001]
  • [Cites] Laryngoscope. 1974 Dec;84(12):2181-94 [4373630.001]
  • [Cites] Scott Med J. 1983 Jan;28(1):64-6 [6301001.001]
  • [Cites] Clin Radiol. 1970 Oct;21(4):403-6 [4320037.001]
  • [Cites] Laryngoscope. 1972 Aug;82(8):1524-32 [4340941.001]
  • (PMID = 23120383.001).
  • [ISSN] 2231-3796
  • [Journal-full-title] Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India
  • [ISO-abbreviation] Indian J Otolaryngol Head Neck Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC3451726
  • [Keywords] NOTNLM ; Digital Subtraction Angiography (DSE) / Juvenile Nasopharyngeal Angiofibroma / Subselective Embolisation (SSE)
  •  go-up   go-down


55. McNiff JM, Subtil A, Cowper SE, Lazova R, Glusac EJ: Cellular digital fibromas: distinctive CD34-positive lesions that may mimic dermatofibrosarcoma protuberans. J Cutan Pathol; 2005 Jul;32(6):413-8
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cellular digital fibromas: distinctive CD34-positive lesions that may mimic dermatofibrosarcoma protuberans.
  • BACKGROUND: Digital fibromas are common benign acral tumors typically reported as angiofibromas (AFs) or acquired digital fibrokeratomas (ADFs).
  • We compared the histologic and immunohistochemical features of these cellular fibromas with five digital AFs, five ADFs, and five digital dermatofibromas.
  • RESULTS: The 14 cellular digital fibromas showed intersecting fascicles of thin delicate bland spindle cells in the superficial reticular dermis with a fibrotic-to-slight myxoid stroma.
  • CONCLUSIONS: These findings suggest that a subset of digital fibromas is characterized by a dense cellular proliferation of CD34-positive spindle cells.
  • Awareness of this variant of digital fibroma and its staining pattern is critical in preventing misdiagnosis as dermatofibrosarcoma protuberans, particularly in superficial biopsies.
  • [MeSH-major] Dermatofibrosarcoma / pathology. Fibroma / pathology. Fingers / pathology. Neoplasms, Connective Tissue / pathology. Skin Neoplasms / pathology


56. Heinrich UR, Brieger J, Gosepath J, Wierzbicka M, Sokolov M, Roth Y, Szyfter W, Bittinger F, Mann WJ: Frequent chromosomal gains in recurrent juvenile nasopharyngeal angiofibroma. Cancer Genet Cytogenet; 2007 Jun;175(2):138-43
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Frequent chromosomal gains in recurrent juvenile nasopharyngeal angiofibroma.
  • Juvenile nasopharyngeal angiofibroma (JNA) is a rare benign tumor, mostly affecting adolescent males.
  • No DNA aneuploidy was detected, a finding in accordance with the generally benign characteristics of JNAs.
  • Autosomal gains in the primary tumor should be further evaluated as markers for a potentially increased risk of recurrence after surgical removal in this entity.
  • [MeSH-major] Angiofibroma / genetics. Chromosome Aberrations. Nasopharyngeal Neoplasms / genetics. Neoplasm Recurrence, Local / genetics

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17556070.001).
  • [ISSN] 0165-4608
  • [Journal-full-title] Cancer genetics and cytogenetics
  • [ISO-abbreviation] Cancer Genet. Cytogenet.
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] United States
  •  go-up   go-down


57. Renukananda GS, Basavaraja PK, Naik AS, Maheshwari M, Balaji NK, Thangavelu G: Atypical angiofibroma of larynx - a case report. Indian J Otolaryngol Head Neck Surg; 2008 Mar;60(1):51-2
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Atypical angiofibroma of larynx - a case report.
  • Primary extra nasopharyngeal angiofibroma of larynx is a very rare tumour.
  • We here by present a case of angiofibroma of larynx affecting the anterior commissure & subglottic region in larynx-a rare site of involvement.

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Am J Otolaryngol. 2003 Nov-Dec;24(6):413-6 [14608576.001]
  • [Cites] J Chin Med Assoc. 2004 Jul;67(7):373-5 [15510937.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 2005 Mar;69(3):415-21 [15733604.001]
  • [Cites] J Laryngol Otol. 2006 Feb;120(2):141-4 [16359575.001]
  • (PMID = 23120500.001).
  • [ISSN] 2231-3796
  • [Journal-full-title] Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India
  • [ISO-abbreviation] Indian J Otolaryngol Head Neck Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC3450725
  • [Keywords] NOTNLM ; Atypical angiofibroma / Extranasopharyngeal angiofibroma / Histolo gy
  •  go-up   go-down


58. Giavroglou C, Constantinidis J, Triaridis S, Daniilidis J, Dimitriadis A: [Angiographic evaluation and embolization of juvenile nasopharyngeal angiofibroma]. HNO; 2007 Jan;55(1):36-41
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Angiographic evaluation and embolization of juvenile nasopharyngeal angiofibroma].
  • [Transliterated title] Juveniles Angiofibrom: Angiographische Diagnostik und präoperative Embolisation.
  • OBJECTIVE: In juvenile nasopharyngeal angiofibroma (JNA), analysis of tumor extension and blood supply is useful for controlling intraoperative bleeding and helps in determining the appropriate surgical approach.
  • [MeSH-major] Angiofibroma / diagnostic imaging. Angiofibroma / therapy. Embolization, Therapeutic / methods. Nasopharyngeal Neoplasms / diagnostic imaging. Nasopharyngeal Neoplasms / therapy. Neoplasm Recurrence, Local / prevention & control

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Eur Radiol. 1998;8(5):756-64 [9601961.001]
  • [Cites] J Laryngol Otol. 1993 Jun;107(6):514-21 [8393907.001]
  • [Cites] Hosp Med. 2004 May;65(5):269-73 [15176142.001]
  • [Cites] Acta Otolaryngol. 2002 Jan;122(1):96-100 [11876606.001]
  • [Cites] HNO. 2003 Dec;51(12):981-5 [14647927.001]
  • [Cites] Ann Otol Rhinol Laryngol. 1970 Dec;79(6):1108-13 [4321405.001]
  • [Cites] Laryngoscope. 1989 Apr;99(4):429-37 [2538688.001]
  • [Cites] Mod Pathol. 1998 Nov;11(11):1122-6 [9831211.001]
  • [Cites] J Laryngol Otol. 1984 May;98(5):489-92 [6325570.001]
  • [Cites] Arch Otolaryngol Head Neck Surg. 1996 Dec;122(12 ):1320-5 [8956743.001]
  • [Cites] Adv Anat Pathol. 2000 Jan;7(1):36-46 [10640200.001]
  • [Cites] HNO. 1996 Mar;44(3):148-52 [8641902.001]
  • [Cites] AJR Am J Roentgenol. 1987 Jan;148(1):209-18 [3024474.001]
  • [Cites] J Laryngol Otol. 1999 Feb;113(2):127-34 [10396561.001]
  • [Cites] Cardiovasc Intervent Radiol. 1995 May-Jun;18(3):158-61 [7648591.001]
  • [Cites] Arch Otolaryngol Head Neck Surg. 1996 Feb;122(2):122-9 [8630204.001]
  • [Cites] Laryngorhinootologie. 2002 Apr;81(4):280-4 [11973680.001]
  • [Cites] Acta Otolaryngol. 1988 Jan-Feb;105(1-2):132-9 [2829500.001]
  • [Cites] Neuroradiology. 1988;30(6):556-60 [2852312.001]
  • [Cites] Otolaryngol Head Neck Surg. 1985 Dec;93(6):803-6 [3003654.001]
  • [Cites] Radiology. 1980 Jul;136(1):119-23 [6247740.001]
  • [Cites] Ann Otol Rhinol Laryngol. 1992 Jun;101(6):469-71 [1319123.001]
  • [Cites] Laryngoscope. 2004 Feb;114(2):291-3 [14755205.001]
  • [Cites] Head Neck Surg. 1981 Mar-Apr;3(4):279-83 [6260711.001]
  • [Cites] Laryngoscope. 1987 Nov;97(11):1319-25 [2823033.001]
  • [Cites] Laryngoscope. 2001 Sep;111(9):1509-11 [11568597.001]
  • (PMID = 16775738.001).
  • [ISSN] 1433-0458
  • [Journal-full-title] HNO
  • [ISO-abbreviation] HNO
  • [Language] ger
  • [Publication-type] Clinical Trial; Journal Article
  • [Publication-country] Germany
  •  go-up   go-down


59. Uyar M, Turanli M, Pak I, Bakir S, Osma U: Extranasopharyngeal angiofibroma originating from the nasal septum: a case report. Kulak Burun Bogaz Ihtis Derg; 2009 Jan-Feb;19(1):41-4
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Extranasopharyngeal angiofibroma originating from the nasal septum: a case report.
  • Angiofibromas (AFs) originate predominantly in the nasopharynx and posterior nasal cavity.
  • Only four cases of extranasopharyngeal angiofibromas arising in the nasal septum have been reported so far.
  • We report here a case of a vascular mass arising from the nasal septum in a 19-year-old boy which was extirpated by submucousal resection endonasally.
  • Histopathology confirmed it to be a case of angiofibroma.
  • [MeSH-major] Angiofibroma / diagnosis. Angiofibroma / surgery. Nasal Septum. Nose Neoplasms / diagnosis. Nose Neoplasms / surgery

  • MedlinePlus Health Information. consumer health - Nasal Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19793047.001).
  • [ISSN] 1300-7475
  • [Journal-full-title] Kulak burun boğaz ihtisas dergisi : KBB = Journal of ear, nose, and throat
  • [ISO-abbreviation] Kulak Burun Bogaz Ihtis Derg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Turkey
  •  go-up   go-down


60. Nicolai P, Villaret AB, Farina D, Nadeau S, Yakirevitch A, Berlucchi M, Galtelli C: Endoscopic surgery for juvenile angiofibroma: a critical review of indications after 46 cases. Am J Rhinol Allergy; 2010 Mar-Apr;24(2):e67-72
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Endoscopic surgery for juvenile angiofibroma: a critical review of indications after 46 cases.
  • BACKGROUND: At present, transnasal endoscopic surgery is considered a viable option in the management of small-intermediate size juvenile angiofibromas (JAs).
  • The lesions were classified according to Andrews (Andrews JC, et al., The surgical management of extensive nasopharyngeal angiofibromas with the infratemporal fossa approach, Laryngoscope 99:429-437, 1989) and Onerci (Onerci M, et al.
  • Juvenile nasopharyngeal angiofibroma: A revised staging system, Rhinology 44:39-45, 2006) staging systems.
  • RESULTS: Lesions were classified as follows: stage I, n = 5; stage II, n = 24; stage IIIa, n = 14; stage IIIb, n = 3 according to Andrews classification system; stage 1, n = 9; stage II, n = 12; stage III, n = 26 according to Onerci's system.
  • In four (8.7%) cases, suspicious residual disease was detected by MRI.
  • [MeSH-major] Angiofibroma / surgery. Endoscopy / methods. Nose Neoplasms / surgery

  • MedlinePlus Health Information. consumer health - Endoscopy.
  • MedlinePlus Health Information. consumer health - Nasal Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20338105.001).
  • [ISSN] 1945-8932
  • [Journal-full-title] American journal of rhinology & allergy
  • [ISO-abbreviation] Am J Rhinol Allergy
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


61. McCluggage WG: A review and update of morphologically bland vulvovaginal mesenchymal lesions. Int J Gynecol Pathol; 2005 Jan;24(1):26-38
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Vulvovaginal mesenchymal lesions composed of morphologically bland spindle-shaped cells often pose a particular diagnostic problem for the surgical pathologist not only because of the rarity of these lesions but also because of the wide array of entities with overlapping morphologic features.
  • Lesions that are relatively specific to the vulvovaginal region include well-known neoplasms such as aggressive angiomyxoma and angiomyofibroblastoma as well as more recently described lesions such as cellular angiofibroma and superficial cervicovaginal myofibroblastoma.
  • [MeSH-minor] Angiofibroma / pathology. Diagnosis, Differential. Female. Humans. Immunohistochemistry. Mesoderm. Myxoma / pathology. Neoplasms, Muscle Tissue / pathology. Polyps / pathology

  • MedlinePlus Health Information. consumer health - Vaginal Cancer.
  • MedlinePlus Health Information. consumer health - Vulvar Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15626915.001).
  • [ISSN] 0277-1691
  • [Journal-full-title] International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists
  • [ISO-abbreviation] Int. J. Gynecol. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 81
  •  go-up   go-down


62. Perez EG, Paranaíba LR, Bonan PR, Orsi Júnior JM, Oliveira AM, Martelli Júnior H: [Tuberous sclerosis: evaluation of myofibroblasts in cutaneous angiofibromas - case report]. An Bras Dermatol; 2010 Jan-Feb;85(1):84-8
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Tuberous sclerosis: evaluation of myofibroblasts in cutaneous angiofibromas - case report].
  • [Transliterated title] Esclerose tuberosa: avaliação de miofibroblastos em angiofibromas cutâneos - relato de caso.
  • Tuberous sclerosis is a rare autosomal dominant disorder.
  • The objective of this study is to describe clinical and histopathological characteristics of tuberous sclerosis and to conduct an immunohistochemical evaluation of myofibroblasts in cutaneous angiofibromas present in this condition.
  • Since alpha-SMA is a specific marker for myofibroblasts, this result suggests that myofibroblasts are not involved in cutaneous angiofibromas present in the tuberous sclerosis case reported.
  • [MeSH-major] Angiofibroma / complications. Angiofibroma / pathology. Fibroblasts / pathology. Skin Neoplasms / complications. Skin Neoplasms / pathology. Tuberous Sclerosis / complications


63. Ardehali MM, Samimi Ardestani SH, Yazdani N, Goodarzi H, Bastaninejad S: Endoscopic approach for excision of juvenile nasopharyngeal angiofibroma: complications and outcomes. Am J Otolaryngol; 2010 Sep-Oct;31(5):343-9
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Endoscopic approach for excision of juvenile nasopharyngeal angiofibroma: complications and outcomes.
  • The purposes of this study are to report the efficacy of the endoscopic approach for juvenile nasopharyngeal angiofibroma (JNA) and to compare its related intra- and postoperative complications with findings from traditional approaches in the literatures.
  • [MeSH-major] Angiofibroma / therapy. Endoscopy. Nasopharyngeal Neoplasms / therapy

  • MedlinePlus Health Information. consumer health - Endoscopy.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Copyright] Copyright 2010 Elsevier Inc. All rights reserved.
  • (PMID = 20015778.001).
  • [ISSN] 1532-818X
  • [Journal-full-title] American journal of otolaryngology
  • [ISO-abbreviation] Am J Otolaryngol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


64. McCluggage WG: Recent developments in vulvovaginal pathology. Histopathology; 2009 Jan;54(2):156-73
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • HMGA2 is useful in the diagnosis of aggressive angiomyxoma and its distinction from mimics, in the evaluation of resection margins and in the assessment of the presence or absence of residual disease in re-excisions.
  • Aggressive angiomyxoma is almost invariably positive with oestrogen and progesterone receptors, and there have been several reports of a dramatic reduction in size following gonadotropin releasing hormone agonist therapy.
  • Recent series of the relatively newly described entities cellular angiofibroma and superficial myofibroblastoma of the lower female genital tract have expanded upon the morphological spectrum of these neoplasms.
  • Recently described mesenchymal lesions at this site include massive oedema and prepubertal vulval fibroma.
  • Gastrointestinal stromal tumours have been described as primary neoplasms in the vagina, and rectovaginal septum and extragastrointestinal stromal tumour should be added to the differential diagnosis of a vulvovaginal mesenchymal lesion.
  • There have been new developments regarding Paget's disease of the vulva with the identification of markers that are useful in diagnosis and evidence that the neoplastic cells represent a proliferation of adnexal stem cells residing in sebaceous units.
  • [MeSH-major] Vaginal Diseases / pathology. Vulvar Diseases / pathology

  • MedlinePlus Health Information. consumer health - Vaginal Diseases.
  • MedlinePlus Health Information. consumer health - Vulvar Disorders.
  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18637148.001).
  • [ISSN] 1365-2559
  • [Journal-full-title] Histopathology
  • [ISO-abbreviation] Histopathology
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 138
  •  go-up   go-down


66. Padilla Parrado M, Díaz Sastre MA, Jiménez Antolín JA, Caro García MA: [Juvenile nasopharyngeal angiofibroma]. An Otorrinolaringol Ibero Am; 2005;32(4):361-71
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Juvenile nasopharyngeal angiofibroma].
  • [Transliterated title] Angiofibroma nasofaringeo juvenil. Situación actual.
  • Juvenile Juvenile nasopharyngeal angiofibroma (JNA) is a benign and highly vascular tumor.
  • [MeSH-major] Angiofibroma / pathology. Nasopharyngeal Neoplasms / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16156366.001).
  • [ISSN] 0303-8874
  • [Journal-full-title] Anales otorrinolaringológicos ibero-americanos
  • [ISO-abbreviation] An Otorrinolaringol Ibero Am
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Spain
  •  go-up   go-down


67. Piperi E, Rohrer MD, Pambuccian SE, Koutlas IG: Vascular solitary fibrous tumor with "floret" cells or giant cell angiofibroma? A lingual example highlighting the overlapping characteristics of these entities and positive immunoreaction for estrogen and progesterone receptors. Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2009 May;107(5):685-90
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Vascular solitary fibrous tumor with "floret" cells or giant cell angiofibroma? A lingual example highlighting the overlapping characteristics of these entities and positive immunoreaction for estrogen and progesterone receptors.
  • Recent literature suggests that giant cell angiofibroma (GCAF) is a variant of solitary fibrous tumor (SFT) and not just a related lesion.
  • We support the present notion that GCAF is a histologic subtype of SFT.
  • [MeSH-major] Angiofibroma / pathology. Solitary Fibrous Tumors / pathology. Tongue Neoplasms / pathology. Vascular Neoplasms / pathology

  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19272802.001).
  • [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; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD34; 0 / Receptors, Estrogen; 0 / Receptors, Progesterone
  •  go-up   go-down


68. Sun Y, Wu Z: [Expression of PCNA, VEGF and bFGF in endothelial cells of juvenile nasopharyngeal angiofibroma]. Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2006 Dec;20(23):1076-8
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Expression of PCNA, VEGF and bFGF in endothelial cells of juvenile nasopharyngeal angiofibroma].
  • OBJECTIVE: To investigate the nature of juvenile nasopharyngeal angiofibroma (JNA).
  • [MeSH-major] Angiofibroma / metabolism. Endothelial Cells / metabolism. Fibroblast Growth Factors / metabolism. Nasopharyngeal Neoplasms / metabolism. Proliferating Cell Nuclear Antigen / metabolism. Vascular Endothelial Growth Factor A / metabolism

  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17285972.001).
  • [Journal-full-title] Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology
  • [ISO-abbreviation] Lin Chuang Er Bi Yan Hou Ke Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] 0 / Proliferating Cell Nuclear Antigen; 0 / VEGFA protein, human; 0 / Vascular Endothelial Growth Factor A; 0 / fibroblast growth factor 13; 62031-54-3 / Fibroblast Growth Factors
  •  go-up   go-down


69. Carlos R, Thompson LD, Netto AC, Pimenta LG, Correia-Silva Jde F, Gomes CC, Gomez RS: Epstein-Barr virus and human herpes virus-8 are not associated with juvenile nasopharyngeal angiofibroma. Head Neck Pathol; 2008 Sep;2(3):145-9
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Epstein-Barr virus and human herpes virus-8 are not associated with juvenile nasopharyngeal angiofibroma.
  • BACKGROUND: Nasopharyngeal angiofibroma (also known as juvenile nasopharyngeal angiofibroma) is a rare fibroblastic tumor with a vascular component that occurs in the nasopharynx and posterolateral nasal wall of adolescent boys.
  • The etiology of nasopharyngeal angiofibroma remains elusive.
  • MATERIALS AND METHODS: Formalin fixed, routinely processed, and paraffin embedded surgical specimens of 15 angiofibromas were submitted to PCR for EBV and HHV-8, while in situ hybridization was also employed for EBV.
  • CONCLUSION: Angiofibroma does not appear to be associated with either HHV-8 or EBV, thereby excluding these viruses as potential etiologic agents.
  • The lack of a correlation between the proliferative index and the age of the patient suggests the proposed puberty induced, testosterone-dependent tumor growth may not play a significant role in tumor development.
  • [MeSH-major] Angiofibroma / virology. Epstein-Barr Virus Infections / virology. Herpesviridae Infections / virology. Herpesvirus 4, Human / isolation & purification. Herpesvirus 8, Human / isolation & purification. Nasopharyngeal Neoplasms / virology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Arch Otolaryngol Head Neck Surg. 2004 Jun;130(6):727-31 [15210553.001]
  • [Cites] Laryngoscope. 2004 Aug;114(8):1500-5 [15280734.001]
  • [Cites] Cancer. 1980 Aug 1;46(3):547-51 [6249485.001]
  • [Cites] Laryngoscope. 1987 Feb;97(2):208-11 [3027480.001]
  • [Cites] J Clin Microbiol. 1990 Oct;28(10):2187-90 [2172284.001]
  • [Cites] Laryngoscope. 1992 Aug;102(8):940-5 [1323004.001]
  • [Cites] Cancer Lett. 1998 May 15;127(1-2):89-93 [9619862.001]
  • [Cites] Mod Pathol. 1998 Nov;11(11):1122-6 [9831211.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 2006 Feb;70(2):227-34 [16023739.001]
  • [Cites] Pathol Int. 2006 Mar;56(3):112-6 [16497243.001]
  • [Cites] J Periodontal Res. 2006 Aug;41(4):235-44 [16827715.001]
  • [Cites] Otolaryngol Head Neck Surg. 2000 Oct;123(4):475-81 [11020189.001]
  • [Cites] Arch Otolaryngol Head Neck Surg. 2000 Jun;126(6):723-5 [10864108.001]
  • [Cites] Cancer Genet Cytogenet. 2007 Jun;175(2):138-43 [17556070.001]
  • [Cites] Laryngoscope. 2002 Feb;112(2):397-401 [11889404.001]
  • (PMID = 20614308.001).
  • [ISSN] 1936-0568
  • [Journal-full-title] Head and neck pathology
  • [ISO-abbreviation] Head Neck Pathol
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / DNA, Viral; 0 / EBV-associated membrane antigen, Epstein-Barr virus; 0 / Ki-67 Antigen; 0 / Viral Matrix Proteins
  • [Other-IDs] NLM/ PMC2807556
  • [Keywords] NOTNLM ; Adolescent / Angiofibroma / EBV / HHV-8 / Immunohistochemistry / In situ hybridization / Ki-67 / MIB / Males / Molecular / Nasopharyngeal juvenile angiofibroma / Neoplasm / Tumor growth / Vascular
  •  go-up   go-down


70. Horowitz G, Gil Z, Kavel O, Smith D, Sela M, Abargel A, Fliss D: [Surgical treatment of maxillary tumors]. Harefuah; 2010 Nov;149(11):704-7, 749
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • METHODS: A total of 174 patients underwent surgery due to neoplasms originating in the maxillary sinus: 118 patients (68%) had malignant and 54 (32%) had benign tumors.
  • RESULTS: The most common malignancy was squamous cell carcinoma (40%), and the most common benign tumor was juvenile nasopharyngeal angiofibroma (36%).
  • Among patients with malignant tumors, 75 are alive without disease (67%), 12 (10%) are alive with disease and 31 (23%) died of disease or other causes.
  • [MeSH-minor] Angiofibroma / mortality. Angiofibroma / surgery. Carcinoma, Squamous Cell / mortality. Carcinoma, Squamous Cell / surgery. Humans. Maxilla / surgery. Melanoma / mortality. Melanoma / surgery. Nasopharyngeal Neoplasms / mortality. Nasopharyngeal Neoplasms / surgery. Retrospective Studies. Sarcoma / mortality. Sarcoma / surgery. Survival Rate

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 21250410.001).
  • [ISSN] 0017-7768
  • [Journal-full-title] Harefuah
  • [ISO-abbreviation] Harefuah
  • [Language] heb
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Israel
  • [Chemical-registry-number] Nasopharyngeal carcinoma
  •  go-up   go-down


76. Eze NN, Wyatt ME, Bray D, Bailey CM, Hartley BE: The midfacial degloving approach to sinonasal tumours in children. Rhinology; 2006 Mar;44(1):36-8
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The procedure allows access to benign and malignant lesions of the sinonasal region with the avoidance of an external scar.
  • Eight children had benign pathology.
  • There were two juvenile angiofibromas, two nasal gliomas, one ossifying fibroma, one fibroma, one fibrous dysplasia and one benign myofibroblastic proliferation.
  • One child had malignant disease in the form of recurrent embryonal rhabdomyosarcoma.

  • MedlinePlus Health Information. consumer health - Nasal Cancer.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16550948.001).
  • [ISSN] 0300-0729
  • [Journal-full-title] Rhinology
  • [ISO-abbreviation] Rhinology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
  •  go-up   go-down


77. Ordóñez-Ordóñez LE, Vergara-Hernández JC, Silva-Rueda R: [Juvenile nasopharyngeal angiofibroma: an atypical case]. Acta Otorrinolaringol Esp; 2008 Oct;59(8):424
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Juvenile nasopharyngeal angiofibroma: an atypical case].
  • [Transliterated title] Angiofibroma nasofaríngeo juvenil: un caso atípico.
  • [MeSH-major] Angiofibroma / radiography. Angiofibroma / surgery. Endoscopy / methods. Nasopharyngeal Neoplasms / radiography. Nasopharyngeal Neoplasms / surgery

  • MedlinePlus Health Information. consumer health - Endoscopy.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18928680.001).
  • [ISSN] 0001-6519
  • [Journal-full-title] Acta otorrinolaringológica española
  • [ISO-abbreviation] Acta Otorrinolaringol Esp
  • [Language] spa
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Spain
  •  go-up   go-down


78. Krstulja M, Kujundzić M, Halaj A, Braut T, Cvjetković N: Radiofrequency-induced thermotherapy of nasopharyngeal angiofibroma and immunohistochemical analysis of vessel proliferation: a case report. J Med Case Rep; 2008;2:278
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Radiofrequency-induced thermotherapy of nasopharyngeal angiofibroma and immunohistochemical analysis of vessel proliferation: a case report.
  • INTRODUCTION: Nasopharyngeal angiofibroma presents with symptoms of nasal obstruction and epistaxis.
  • CASE PRESENTATION: A 52-year-old man underwent surgery for nasopharyngeal angiofibroma after adjuvant radiofrequency-induced thermotherapy.
  • To the best of the authors' knowledge, this is the first case of angiofibroma with clinical follow-up after thermocoagulation therapy supported by quantitative, double immunohistochemistry.
  • We found this case of angiofibroma to be of interest owing to the presentation of symptoms leading to biopsy, the pathohistological observations obtained with synchronous Ki67/cluster of differentiation 34 and Ki67/smooth muscle actin immunohistochemistry and high pericyte proliferation.
  • CONCLUSION: Coagulation of angiofibroma vessels followed by acquisition of a thick mantle of pericytes in a patient with a nasopharyngeal growth suggests that radiofrequency-induced thermotherapy could be a useful, palliative therapy for bleeding nasopharyngeal angiofibroma, supporting vessel maturation prior to surgical tumor removal.

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] J Clin Pathol. 2007 Jul;60(7):798-803 [16816171.001]
  • [Cites] Int J Pediatr Otorhinolaryngol. 2005 Mar;69(3):415-21 [15733604.001]
  • [Cites] Laryngoscope. 1997 Jul;107(7):926-31 [9217133.001]
  • [Cites] Circ Res. 1997 Apr;80(4):444-51 [9118474.001]
  • [Cites] Arch Otorhinolaryngol. 1980;226(3):187-97 [7458752.001]
  • [Cites] Adv Anat Pathol. 2000 Jan;7(1):36-46 [10640200.001]
  • [Cites] Development. 2002 Jun;129(11):2773-83 [12015303.001]
  • [Cites] Am J Med Genet. 2002 Apr 15;109(1):22-35 [11932989.001]
  • [Cites] Otolaryngol Head Neck Surg. 2000 Oct;123(4):475-81 [11020189.001]
  • [Cites] Arch Pathol Lab Med. 2000 Mar;124(3):406-10 [10705395.001]
  • [Cites] Arch Pathol Lab Med. 2003 Nov;127(11):1480-4 [14567719.001]
  • (PMID = 18706100.001).
  • [ISSN] 1752-1947
  • [Journal-full-title] Journal of medical case reports
  • [ISO-abbreviation] J Med Case Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2535598
  •  go-up   go-down


79. Chen E, Fletcher CD: Cellular angiofibroma with atypia or sarcomatous transformation: clinicopathologic analysis of 13 cases. Am J Surg Pathol; 2010 May;34(5):707-14
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cellular angiofibroma with atypia or sarcomatous transformation: clinicopathologic analysis of 13 cases.
  • Cellular angiofibroma is a mesenchymal neoplasm that is characterized by a bland spindle cell component, morphologically reminiscent of spindle cell lipoma, and thick-walled vessels.
  • An earlier study of 51 cases from our group showed that the tumor follows a benign course without any tendency for recurrence.
  • The biologic significance of atypia or sarcomatous transformation in cellular angiofibroma remains uncertain.
  • In this study, we characterized clinicopathologic features in 13 cases of cellular angiofibroma with morphologic atypia or sarcomatous transformation.
  • Thirteen cases with atypia or sarcomatous transformation among 154 usual cellular angiofibromas identified between 1993 and 2009 were retrieved from consultation files.
  • There were 4 cases of cellular angiofibroma with atypia.
  • Three showed severely atypical cells as scattered foci within the cellular angiofibroma.
  • There were 9 cases of cellular angiofibroma with morphologic features of sarcomatous transformation.
  • Three of these 9 cases showed discrete nodule(s) closely resembling atypical lipomatous tumor within usual cellular angiofibroma.
  • By immunohistochemistry, atypical cells and sarcomatous areas showed either multifocal or more diffuse p16 expression compared with either scattered or negative expression in the conventional cellular angiofibroma.
  • One patient died of metastatic carcinoma of unknown primary site 27 months after the diagnosis of cellular angiofibroma with sarcomatous transformation.
  • Cellular angiofibroma with atypia or morphologic sarcomatous transformation occurs predominantly in the subcutaneous tissue of the vulva and, as yet, shows no evident tendency to recur based on limited clinical follow-up available for 7 cases.
  • The sarcomatous component can show variable features including atypical lipomatous tumor, pleomorphic liposarcoma, and pleomorphic sarcoma NOS.
  • [MeSH-major] Angiofibroma / pathology. Cell Transformation, Neoplastic. Sarcoma / pathology. Soft Tissue Neoplasms / pathology

  • MedlinePlus Health Information. consumer health - Soft Tissue Sarcoma.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20305534.001).
  • [ISSN] 1532-0979
  • [Journal-full-title] The American journal of surgical pathology
  • [ISO-abbreviation] Am. J. Surg. Pathol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
  •  go-up   go-down


80. Shcherbenko OI, Rodionov MV, Lebedev VA, Kliachkina NB: [Efficacy of remote gamma-therapy in patients with juvenile angiofibroma of the base of the skull]. Vestn Otorinolaringol; 2008;(3):26-8
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Efficacy of remote gamma-therapy in patients with juvenile angiofibroma of the base of the skull].
  • The results of radiation therapy of 48 patients with juvenile nasopharyngeal angiofibroma were analysed.
  • [MeSH-major] Angiofibroma / radiotherapy. Gamma Rays / therapeutic use. Skull Base Neoplasms / radiotherapy

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18833092.001).
  • [ISSN] 0042-4668
  • [Journal-full-title] Vestnik otorinolaringologii
  • [ISO-abbreviation] Vestn. Otorinolaringol.
  • [Language] rus
  • [Publication-type] Comparative Study; English Abstract; Journal Article
  • [Publication-country] Russia (Federation)
  •  go-up   go-down


81. Satgé D, Vidalo E, Desfarges F, de Geeter B: A third case of cardiac neoplasm in a fetus with Beckwith-Wiedemann syndrome: epicardial angiofibroma. Fetal Diagn Ther; 2005 Jan-Feb;20(1):44-7
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A third case of cardiac neoplasm in a fetus with Beckwith-Wiedemann syndrome: epicardial angiofibroma.
  • OBJECTIVE: A personal observation of a 20-week-old fetus with Beckwith-Wiedemann syndrome (BWS) presenting epicardial angiofibroma prompted us to evaluate cardiac neoplasms in this genetic condition.
  • [MeSH-major] Angiofibroma / etiology. Beckwith-Wiedemann Syndrome / complications. Fetal Diseases. Heart Neoplasms / etiology. Pericardium
  • [MeSH-minor] Adult. Female. Hamartoma / etiology. Hamartoma / pathology. Heart Diseases / etiology. Heart Diseases / pathology. Humans. Pregnancy. Pregnancy Trimester, First

  • Genetic Alliance. consumer health - Beckwith-Wiedemann Syndrome.
  • MedlinePlus Health Information. consumer health - Fetal Health and Development.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15608459.001).
  • [ISSN] 1015-3837
  • [Journal-full-title] Fetal diagnosis and therapy
  • [ISO-abbreviation] Fetal. Diagn. Ther.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Switzerland
  • [Number-of-references] 15
  •  go-up   go-down


82. Spielmann PM, Adamson R, Cheng K, Sanderson RJ: Juvenile nasopharyngeal angiofibroma: spontaneous resolution. Ear Nose Throat J; 2008 Sep;87(9):521-3
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Juvenile nasopharyngeal angiofibroma: spontaneous resolution.
  • Juvenile nasopharyngeal angiofibroma is a rare, benign tumor that occurs most often in adolescent males.
  • We report the case of a 17-year-old male who presented in 1995 with a mass filling the left posterior nasal cavity.
  • A diagnosis of juvenile nasopharyngeal angiofibroma was obtained with computed tomography and magnetic resonance imaging.
  • [MeSH-major] Angiofibroma / diagnosis. Nasopharyngeal Neoplasms / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18800325.001).
  • [ISSN] 1942-7522
  • [Journal-full-title] Ear, nose, & throat journal
  • [ISO-abbreviation] Ear Nose Throat J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 20
  •  go-up   go-down


83. Nomura K, Shimomura A, Awataguchi T, Murakami K, Kobayashi T: A case of angiofibroma originating from the inferior nasal turbinate. Auris Nasus Larynx; 2006 Jun;33(2):191-3
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A case of angiofibroma originating from the inferior nasal turbinate.
  • Angiofibromas are nasopharyngeal tumors mostly seen in adolescent males.
  • Extranasopharyngeal angiofibromas, although rare, have been reported.
  • We report a case of extranasopharyngeal angiofibroma arising from the inferior turbinate of a 62-year-old male.
  • Previous extranasopharyngeal angiofibromas research was reviewed.
  • [MeSH-major] Angiofibroma / pathology. Nasopharyngeal Neoplasms / pathology. Turbinates / pathology

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16310998.001).
  • [ISSN] 0385-8146
  • [Journal-full-title] Auris, nasus, larynx
  • [ISO-abbreviation] Auris Nasus Larynx
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Netherlands
  •  go-up   go-down


84. Joo D, Chhetri DK, Wang MB: Endoscopic removal of juvenile nasopharyngeal angiofibromas: a video presentation. Laryngoscope; 2008 Jun;118(6):e1-3
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Endoscopic removal of juvenile nasopharyngeal angiofibromas: a video presentation.
  • OBJECTIVES/HYPOTHESIS: Juvenile nasal angiogibroma (JNA) is a relatively rare, benign neoplasm generally seen in prepubertal and adolescent males.
  • Through the use of a brief video presentation, participants will be able to visualize the endoscopic technique.
  • RESULTS: A video demonstration is presented of a patient with a 3.5 cm JNA who underwent successful endoscopic, endonasal excision.
  • The tumor was resected en bloc with minimal bleeding.
  • [MeSH-major] Angiofibroma / surgery. Endoscopy / methods. Nasal Cavity. Nasopharyngeal Neoplasms / surgery. Nose Neoplasms / surgery. Paranasal Sinus Neoplasms / surgery

  • MedlinePlus Health Information. consumer health - Endoscopy.
  • MedlinePlus Health Information. consumer health - Nasal Cancer.
  • NCI CPTAC Assay Portal. NCI CPTAC Assay Portal .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18391769.001).
  • [ISSN] 1531-4995
  • [Journal-full-title] The Laryngoscope
  • [ISO-abbreviation] Laryngoscope
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


85. de Vries PJ, Hunt A, Bolton PF: The psychopathologies of children and adolescents with tuberous sclerosis complex (TSC): a postal survey of UK families. Eur Child Adolesc Psychiatry; 2007 Feb;16(1):16-24
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Tuberous Sclerosis Complex (TSC) is a multi-system genetic disorder associated with a wide range of physical features and very high rates of numerous neurocognitive manifestations.
  • Children with MR were significantly more likely to have an autism spectrum disorder, attention deficit-related symptoms and speech and language difficulties.
  • They were more likely to have a history of epilepsy, facial angiofibromata and shagreen patches and tended to have a greater number of physical features of the disorder.
  • However, about one third of the children without MR had features suggestive of a developmental disorder.
  • These findings show that TSC can place any child or adolescent at significantly increased risk of a range of neurodevelopmental disabilities.

  • Genetic Alliance. consumer health - Tuberous sclerosis.
  • MedlinePlus Health Information. consumer health - Tuberous Sclerosis.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • [Cites] Brain. 2002 Jun;125(Pt 6):1247-55 [12023313.001]
  • [Cites] Psychol Med. 1999 Jul;29(4):769-86 [10473304.001]
  • [Cites] Int Rev Psychiatry. 2003 Feb-May;15(1-2):185-7 [12745331.001]
  • [Cites] Am J Hum Genet. 2001 Jan;68(1):64-80 [11112665.001]
  • [Cites] J Child Psychol Psychiatry. 1997 Jul;38(5):581-6 [9255702.001]
  • [Cites] Dev Med Child Neurol. 1996 Feb;38(2):139-45 [8603781.001]
  • [Cites] Eur Child Adolesc Psychiatry. 2005 Jul;14(4):183-90 [15981129.001]
  • [Cites] Ann Hum Genet. 1994 May;58(Pt 2):107-27 [7979156.001]
  • [Cites] Psychol Med. 2003 Feb;33(2):335-44 [12622312.001]
  • [Cites] J Autism Dev Disord. 1989 Jun;19(2):185-212 [2745388.001]
  • [Cites] J Med Genet. 2004 Mar;41(3):203-7 [14985384.001]
  • [Cites] J Child Neurol. 2004 Sep;19(9):666-74 [15563012.001]
  • [Cites] Dev Med Child Neurol. 1983 Jun;25(3):353-7 [6192027.001]
  • [Cites] BMJ. 1999 Apr 17;318(7190):1019-20 [10205080.001]
  • [Cites] J Med Genet. 1994 Oct;31(10):761-5 [7837252.001]
  • [Cites] J Autism Dev Disord. 1994 Oct;24(5):659-85 [7814313.001]
  • [Cites] Ment Retard Dev Disabil Res Rev. 2004;10(2):126-31 [15362169.001]
  • [Cites] Dev Med Child Neurol. 1987 Apr;29(2):190-8 [3582788.001]
  • [Cites] Dev Med Child Neurol. 1994 Jan;36(1):50-6 [8132114.001]
  • [Cites] Dev Med Child Neurol. 1996 Feb;38(2):146-55 [8603782.001]
  • [Cites] Lancet. 1997 Feb 8;349(9049):392-5 [9033466.001]
  • [Cites] J Med Genet. 2000 Feb;37(2):156-7 [10712110.001]
  • [Cites] J Intellect Disabil Res. 2003 Jan;47(Pt 1):51-8 [12558695.001]
  • [Cites] J Child Neurol. 1998 Dec;13(12 ):624-8 [9881533.001]
  • [Cites] Hum Mol Genet. 1997 Nov;6(12):2155-61 [9328481.001]
  • [Cites] J Med Genet. 2000 May;37(5):E3 [10807702.001]
  • [Cites] J Autism Dev Disord. 1993 Jun;23(2):323-39 [8331050.001]
  • [Cites] J Child Psychol Psychiatry. 2000 May;41(4):491-502 [10836679.001]
  • [Cites] J Intellect Disabil Res. 1993 Feb;37 ( Pt 1):41-51 [7681710.001]
  • (PMID = 17268883.001).
  • [ISSN] 1018-8827
  • [Journal-full-title] European child & adolescent psychiatry
  • [ISO-abbreviation] Eur Child Adolesc Psychiatry
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
  •  go-up   go-down


86. Maggiani F, Debiec-Rychter M, Vanbockrijck M, Sciot R: Cellular angiofibroma: another mesenchymal tumour with 13q14 involvement, suggesting a link with spindle cell lipoma and (extra)-mammary myofibroblastoma. Histopathology; 2007 Sep;51(3):410-2
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Cellular angiofibroma: another mesenchymal tumour with 13q14 involvement, suggesting a link with spindle cell lipoma and (extra)-mammary myofibroblastoma.
  • [MeSH-major] Angiofibroma / pathology. Chromosome Deletion. Chromosomes, Human, Pair 13 / genetics. Mesoderm / pathology

  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17727484.001).
  • [ISSN] 0309-0167
  • [Journal-full-title] Histopathology
  • [ISO-abbreviation] Histopathology
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Antigens, CD34; 0 / Desmin; 0 / Retinoblastoma Protein
  •  go-up   go-down


87. Janaki MG, Nirmala S, Rajeev AG: Nasopharyngeal angiofibroma treated with radiotherapy. J Cancer Res Ther; 2007 Apr-Jun;3(2):100-1
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Nasopharyngeal angiofibroma treated with radiotherapy.
  • Nasopharyngeal angiofibroma is a rare, highly vascular, benign, locally aggressive tumor, affecting boys of adolescent age.
  • Although surgery is the treatment of choice in early cases, considerable debate exists regarding the treatment of advanced disease with intracranial extension.
  • We are herewith reporting a case of nasopharyngeal angiofibroma who showed complete hemostasis and improvement in vision to radiotherapy.
  • [MeSH-major] Angiofibroma / radiotherapy. Nasopharyngeal Neoplasms / radiotherapy

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17998732.001).
  • [ISSN] 1998-4138
  • [Journal-full-title] Journal of cancer research and therapeutics
  • [ISO-abbreviation] J Cancer Res Ther
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] India
  •  go-up   go-down


88. Snyderman CH, Pant H, Carrau RL, Gardner P: A new endoscopic staging system for angiofibromas. Arch Otolaryngol Head Neck Surg; 2010 Jun;136(6):588-94
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A new endoscopic staging system for angiofibromas.
  • OBJECTIVE: To develop a new staging system for juvenile nasopharyngeal angiofibroma that reflects changes in surgical approaches (endonasal), route of intracranial extension, and the extent of vascular supply from the internal carotid artery.
  • PATIENTS: Patients undergoing endoscopic endonasal surgery for juvenile nasopharyngeal angiofibroma at the University of Pittsburgh Medical Center (UPMC), Pittsburgh, Pennsylvania, from 1998 through 2008.
  • CONCLUSIONS: Tumor size and extent of sinus disease are less important in predicting complete tumor removal with endonasal surgical techniques.
  • The UPMC staging system for juvenile nasopharyngeal angiofibroma accounts for 2 important prognostic factors, route of cranial base extension, and vascularity and is applicable to endoscopic or open approaches.
  • [MeSH-major] Angiofibroma / pathology. Endoscopy. Nasopharyngeal Neoplasms / pathology. Neoplasm Staging / standards


89. Parikh SR, Cuellar H, Sadoughi B, Aroniadis O, Fried MP: Indications for image-guidance in pediatric sinonasal surgery. Int J Pediatr Otorhinolaryngol; 2009 Mar;73(3):351-6
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Indications for surgery included chronic (30.3%) and acute (12.1%) rhinosinusitis, nasopharyngeal angiofibroma (9.1%), allergic rhinosinusitis (9.1%) and allergic fungal sinusitis (9.1%).
  • In our population, image-guidance was only used for advanced sinonasal procedures where there was an anatomic abnormality or disease that extended to the sphenoid sinus, frontal sinus, orbit, or skull base.

  • MedlinePlus Health Information. consumer health - Endoscopy.
  • COS Scholar Universe. author profiles.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 19157578.001).
  • [ISSN] 1872-8464
  • [Journal-full-title] International journal of pediatric otorhinolaryngology
  • [ISO-abbreviation] Int. J. Pediatr. Otorhinolaryngol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Ireland
  •  go-up   go-down


90. Surace D, Blandamura S, Bernardini FP, Galan A, Lo Giudice G: Unusual presentation of giant cell angiofibroma of the eyelids. Eur J Ophthalmol; 2010 Nov-Dec;20(6):1073-5
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Unusual presentation of giant cell angiofibroma of the eyelids.
  • PURPOSE: To describe a case of bilateral eyelid-confined giant cell angiofibroma (GCAF) in a patient with a slowly progressive bilateral eyelid swelling.
  • CONCLUSIONS: Giant cell angiofibroma involving the eyelid is rare and can represent a diagnostic and therapeutic challenge to the ophthalmologist.
  • [MeSH-major] Angiofibroma / diagnosis. Eyelid Neoplasms / diagnosis. Giant Cell Tumors / diagnosis

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20623470.001).
  • [ISSN] 1724-6016
  • [Journal-full-title] European journal of ophthalmology
  • [ISO-abbreviation] Eur J Ophthalmol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Neoplasm Proteins
  •  go-up   go-down


91. Igaz P: MEN1 clinical background. Adv Exp Med Biol; 2009;668:1-15
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Beside these three, several other endocrine (adrenocortical, foregut carcinoid) and nonendocrine (lipoma, angiofibroma, collagenoma, ependymoma, meningioma) tumors have been described to be associated with this syndrome.
  • Both familial and sporadic forms of the disease are known.
  • Both benign (parathyroid, anterior pituitary) and malignant (gastrinoma, glucagonoma) lesions may develop in MEN1 patients.
  • Regular surveillance of MEN1 gene mutation carriers is necessary to reveal disease manifestations.
  • [MeSH-minor] Adult. Child. Child, Preschool. Diagnosis, Differential. Genetic Predisposition to Disease. Genetic Testing. Humans. Middle Aged. Multiple Endocrine Neoplasia Type 2a / genetics. Multiple Endocrine Neoplasia Type 2a / pathology. Multiple Endocrine Neoplasia Type 2a / physiopathology. Mutation. Young Adult

  • NCI CPTC Antibody Characterization Program. NCI CPTC Antibody Characterization Program .
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 20175448.001).
  • [ISSN] 0065-2598
  • [Journal-full-title] Advances in experimental medicine and biology
  • [ISO-abbreviation] Adv. Exp. Med. Biol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


92. Timotin L, Sarrot-Reynauld F, Lantuejoul S, Pasquier B, Massot C, Ashraf A, Borgel F: [Tuberous sclerosis without mental impairment, diagnosed in adulthood]. Rev Med Interne; 2005 Jun;26(6):511-3
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Transliterated title] Sclérose tubéreuse de Bourneville sans altération intellectuelle, diagnostiquée à l'âge adulte.
  • EXEGESIS: We report a case of TSC diagnosed in a 33-year-old man, without any known family history of phakomatosis, presenting with facial angiofibromas, hypomelanotic macules, a giant-cell astrocytoma and retinal phakomas without any mental impairment or epilepsy.
  • CONCLUSION: TSC may occur in patients who do not have any family history of phakomatosis because de novo mutations are frequent.
  • Facial angiofibromas are highly suggestive of tuberous sclerosis complex.

  • Genetic Alliance. consumer health - Tuberous sclerosis.
  • MedlinePlus Health Information. consumer health - Tuberous Sclerosis.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15936480.001).
  • [ISSN] 0248-8663
  • [Journal-full-title] La Revue de medecine interne
  • [ISO-abbreviation] Rev Med Interne
  • [Language] FRE
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  •  go-up   go-down


93. Sen C, Alvarez G, Dagotto E: Competing ferromagnetic and charge-ordered states in models for manganites: the origin of the colossal magnetoresistance effect. Phys Rev Lett; 2007 Mar 23;98(12):127202
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • The one-orbital model for manganites with cooperative phonons and superexchange coupling JAF is investigated via large-scale Monte Carlo simulations.

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17501153.001).
  • [ISSN] 0031-9007
  • [Journal-full-title] Physical review letters
  • [ISO-abbreviation] Phys. Rev. Lett.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


94. Belcadhi M, Mani R, Harzallah M, Bouaouina N, Bouzouita K: [Nasopharyngeal angiofibroma with intracranial extension: situating the chemotherapy-radiotherapy association]. Cancer Radiother; 2008 Sep;12(5):385-8
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Nasopharyngeal angiofibroma with intracranial extension: situating the chemotherapy-radiotherapy association].
  • [Transliterated title] L'angiofibrome nasopharyngien avec extension intracrânienne : place de l'association chimiothérapie-radiothérapie.
  • Nasopharyngeal angiofibroma is a locally aggressive, although histologically benign, vascular neoplasm.
  • Surgery is considered as the primary treatment of nasopharyngeal angiofibroma.
  • We report a rare case of nasopharyngeal angiofibroma, further complicated with a Kennedy syndrome in a 34 year-old women.
  • We discuss the relevance and outcome of the association chemotherapy-radiotherapy in the treatment of nasopharyngeal angiofibromas with a consistent intracranial extension (stage III B of Arch Otolaryngol Head Neck Surg 122 (2003) 122-129).
  • [MeSH-major] Angiofibroma / drug therapy. Angiofibroma / radiotherapy. Brain Neoplasms / radiotherapy. Nasopharyngeal Neoplasms / drug therapy. Nasopharyngeal Neoplasms / radiotherapy

  • MedlinePlus Health Information. consumer health - Brain Tumors.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 18339570.001).
  • [ISSN] 1278-3218
  • [Journal-full-title] Cancer radiothérapie : journal de la Société française de radiothérapie oncologique
  • [ISO-abbreviation] Cancer Radiother
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
  •  go-up   go-down


95. Zozulya YP, Slin'ko EI, Al-Qashqish II: Spinal arteriovenous malformations: new classification and surgical treatment. Neurosurg Focus; 2006;20(5):E7
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Spinal arteriovenous malformations: new classification and surgical treatment.
  • Insufficient study of this disease is connected with the complexity of its diagnosis, which restricts the development of surgical treatments that are differentiated according to the type of malformation.
  • Great difficulties are caused by the lack of a clear structural-hemodynamic classification of spinal arteriovenous malformations (AVMs).
  • At present the classification created between 1991 and 1998 by the combined efforts of different authors is the most widely used one.
  • According to this classification, four categories are distinguishable: Type I, dural arteriovenous fistulas (AVFs); Type II, intramedullary glomus AVMs; Type III, juvenile or combined AVMs; and Type IV, intradural perimedullary AVFs.
  • Vascular tumors are also classified, as follows: hemangiomas, hemangioblastomas, angiosarcomas, hemangiopericytomas, angiofibromas, angiolipomas, and hemangioendotheliomas, as well as cavernous malformations.
  • For spinal vascular malformations we devised a classification that took into account the aforementioned features of AVMs: the anatomical characteristics of a malformation and its angiostructural and hemodynamic features.
  • [MeSH-major] Arteriovenous Malformations / classification. Arteriovenous Malformations / surgery. Neurosurgical Procedures. Spinal Cord / blood supply

  • MedlinePlus Health Information. consumer health - Arteriovenous Malformations.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16711664.001).
  • [ISSN] 1092-0684
  • [Journal-full-title] Neurosurgical focus
  • [ISO-abbreviation] Neurosurg Focus
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 22
  •  go-up   go-down


96. Zhang QF, She CP, Tong YF, Jin Y, Zhang XR: [Endoscopic surgery using the low-temperature plasma radiofrequency for nasopharyngeal angiofibroma]. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2010 Jul;45(7):578-81
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Endoscopic surgery using the low-temperature plasma radiofrequency for nasopharyngeal angiofibroma].
  • OBJECTIVE: To evaluate the feasibility of endoscopic surgery using the low-temperature plasma radiofrequency for nasopharyngeal angiofibroma (NA).
  • CONCLUSIONS: Endoscopic surgery using low-temperature plasma radiofrequency for nasopharyngeal angiofibroma has many advantages such as less bleeding and total tumor removal.
  • It is a minimally invasive surgical method for nasopharyngeal angiofibroma.
  • [MeSH-major] Angiofibroma / surgery. Catheter Ablation / methods. Endoscopy. Nasopharyngeal Neoplasms / surgery

  • MedlinePlus Health Information. consumer health - Endoscopy.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 21055057.001).
  • [ISSN] 1673-0860
  • [Journal-full-title] Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
  • [ISO-abbreviation] Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Evaluation Studies; Journal Article
  • [Publication-country] China
  •  go-up   go-down


97. Rosón E, Flórez A, Feal C, De La Torre C, García-Doval I, Abalde T, Cruces M: Progressive nodular histiocytoma associated with thrombocytopenia with absent radii (TAR syndrome) and angiofibromas. Acta Derm Venereol; 2006;86(4):348-50
PDF icon [Fulltext service] Download fulltext PDF of this article and others, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Progressive nodular histiocytoma associated with thrombocytopenia with absent radii (TAR syndrome) and angiofibromas.
  • Moreover, the patient had numerous smooth erythematous papules on her chin and around her nose, which were diagnosed histologically as angiofibromas.
  • To our knowledge progressive nodular histiocytoma has not been reported previously associated either with TAR syndrome or with angiofibromas.
  • [MeSH-major] Angiofibroma / complications. Ectromelia / complications. Histiocytoma / pathology. Radius / abnormalities. Skin Diseases / pathology. Thrombocytopenia / complications

  • Genetic Alliance. consumer health - TAR syndrome.
  • MedlinePlus Health Information. consumer health - Skin Conditions.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16874423.001).
  • [ISSN] 0001-5555
  • [Journal-full-title] Acta dermato-venereologica
  • [ISO-abbreviation] Acta Derm. Venereol.
  • [Language] eng
  • [Databank-accession-numbers] OMIM/ 274000
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Norway
  •  go-up   go-down


98. Rudakov AF: [The operation for juvenile angiofibroma of the nasopharynx as in terms of anesthesiology and critical care]. Vestn Otorinolaringol; 2005;(4):48-9
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [The operation for juvenile angiofibroma of the nasopharynx as in terms of anesthesiology and critical care].
  • [MeSH-major] Anesthesiology / methods. Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 16091727.001).
  • [ISSN] 0042-4668
  • [Journal-full-title] Vestnik otorinolaringologii
  • [ISO-abbreviation] Vestn. Otorinolaringol.
  • [Language] rus
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Russia (Federation)
  •  go-up   go-down


99. Andrade NA, Pinto JA, Nóbrega Mde O, Aguiar JE, Aguiar TF, Vinhaes ES: Exclusively endoscopic surgery for juvenile nasopharyngeal angiofibroma. Otolaryngol Head Neck Surg; 2007 Sep;137(3):492-6
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Exclusively endoscopic surgery for juvenile nasopharyngeal angiofibroma.
  • OBJECTIVE: To present the indications of nasal endoscopic surgery for treating juvenile nasopharyngeal angiofibroma (JNA).
  • According to the classification of Andrews et al, eight patients were stage I and four patients were stage II.
  • [MeSH-major] Angiofibroma / surgery. Endoscopy. Nasopharyngeal Neoplasms / surgery

  • MedlinePlus Health Information. consumer health - Endoscopy.
  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 17765782.001).
  • [ISSN] 0194-5998
  • [Journal-full-title] Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery
  • [ISO-abbreviation] Otolaryngol Head Neck Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  •  go-up   go-down


100. Hanamure Y, Tanaka N, Kawabata T, Kasano F, Kashima N: [Juvenile nasopharyngeal angiofibroma: stage and surgical approach]. Nihon Jibiinkoka Gakkai Kaiho; 2005 May;108(5):513-21
PDF icon [Fulltext service] Get downloadable fulltext PDFs of articles closely matching to this article, as many as you want.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Juvenile nasopharyngeal angiofibroma: stage and surgical approach].
  • Juvenile nasopharyngeal angiofibromas (JNAs) are benign tumors that occasionally invade the pterygopalatine fossa, infratemporal fossa, or middle cranial fossa.
  • [MeSH-major] Angiofibroma / pathology. Angiofibroma / surgery. Nasopharyngeal Neoplasms / pathology. Nasopharyngeal Neoplasms / surgery. Otorhinolaryngologic Surgical Procedures / methods

  • [Email] Email this result item
    Email the results to the following email address:   [X] Close
  • (PMID = 15952338.001).
  • [ISSN] 0030-6622
  • [Journal-full-title] Nihon Jibiinkoka Gakkai kaiho
  • [ISO-abbreviation] Nippon Jibiinkoka Gakkai Kaiho
  • [Language] jpn
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Japan
  • [Number-of-references] 35
  •  go-up   go-down






Advertisement