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1. Gołabek W, Szymańska A, Siwiec H, Trojanowski P: [Transpalatal approach for juvenile angiofibroma]. Otolaryngol Pol; 2008;62(1):16-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Transpalatal approach for juvenile angiofibroma].
  • INTRODUCTION: Juvenile nasopharyngeal angiofibromas (JNA) are highly vascular, locally invasive tumours which originate in the sphenopalatine foramen.
  • The aim of this study was to evaluate the transpalatal approach for juvenile angiofibroma.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Otorhinolaryngologic Surgical Procedures / methods. Paranasal Sinus Neoplasms / surgery

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  • (PMID = 18637415.001).
  • [ISSN] 0030-6657
  • [Journal-full-title] Otolaryngologia polska = The Polish otolaryngology
  • [ISO-abbreviation] Otolaryngol Pol
  • [Language] pol
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Poland
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2. 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
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  • [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

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  • (PMID = 20464093.001).
  • [ISSN] 1806-4841
  • [Journal-full-title] Anais brasileiros de dermatologia
  • [ISO-abbreviation] An Bras Dermatol
  • [Language] por
  • [Publication-type] Case Reports; English Abstract; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Brazil
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3. Lai V, Wong YC, Lam WY, Tsui WC, Luk SH: Inflammatory myofibroblastic tumor of the nasal cavity. AJNR Am J Neuroradiol; 2007 Jan;28(1):135-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Inflammatory myofibroblastic tumor (IMT) is a rare tumor with a variable natural history and biologic behavior, ranging from completely benign to malignant with fatal outcome.
  • We report a case of benign IMT in the left nasal cavity with radiologic features mimicking angiofibroma.
  • We also demonstrate the hypervascular nature of this disease on angiography and the contribution of preoperative embolization in assisting surgical excision and minimizing the potential uncontrolled intraoperative bleeding.

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  • (PMID = 17213441.001).
  • [ISSN] 0195-6108
  • [Journal-full-title] AJNR. American journal of neuroradiology
  • [ISO-abbreviation] AJNR Am J Neuroradiol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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4. de Brito Macedo Ferreira LM, Gomes EF, Azevedo JF, Souza JR, de Paula Araújo R, do Nascimento Rios AS: Endoscopic surgery of nasopharyngeal angiofibroma. Braz J Otorhinolaryngol; 2006 Jul-Aug;72(4):475-80

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Endoscopic surgery of nasopharyngeal angiofibroma.
  • Nasopharyngeal angiofibroma is a vascular benign tumor that affects young men, and surgery is the treatment of choice.
  • Endoscopic surgery has been used to excise tumors in their initial stages, when there is no evidence of residual or recurrent disease.
  • AIM: The aim of this study is to evaluate the endoscopic approach preceded by tumor embolization as treatment option for stages II to III angiofibroma.
  • CONCLUSION: Based on the results, we may conclude that the endoscopic approach, when preceded by embolization, is effective to treat angiofibromas in their initial stages, with reduced postoperative morbidity.
  • [MeSH-major] Angiofibroma / therapy. Nasopharyngeal Neoplasms / therapy

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  • (PMID = 17143426.001).
  • [ISSN] 1808-8694
  • [Journal-full-title] Brazilian journal of otorhinolaryngology
  • [ISO-abbreviation] Braz J Otorhinolaryngol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Brazil
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5. Das S, Kirsch CF: Imaging of lumps and bumps in the nose: a review of sinonasal tumours. Cancer Imaging; 2005;5:167-77

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Sinonasal disease is one of the most common clinical head and neck pathologies.
  • Although sinus tumours are rare, they portend a poor prognosis, often due to advanced disease at diagnosis.
  • Like most neoplasms, early detection improves prognosis, therefore clinicians and radiologists should be aware of features separating tumours from inflammatory sinus disease.
  • Benign neoplasms reviewed include osteoma, inverting papilloma, and juvenile nasal angiofibroma.

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  • [Copyright] International Cancer Imaging Society.
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  • (PMID = 16361146.001).
  • [ISSN] 1470-7330
  • [Journal-full-title] Cancer imaging : the official publication of the International Cancer Imaging Society
  • [ISO-abbreviation] Cancer Imaging
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 73
  • [Other-IDs] NLM/ PMC1665243
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6. 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

  • [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

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  • (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
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7. Olubunmi OA: Misdiagnosis of tuberous sclerosis in a Nigerian girl: a case report and review of literature. Ann Afr Med; 2010 Apr-Jun;9(2):95-101
Hazardous Substances Data Bank. VALPROIC ACID .

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Tuberous sclerosis is a rare neuro-cutaneous syndrome, one of the phakomatosis, characterized by facial angiofibromas (adenoma sebaceum), mental retardation and epilepsy.
  • [MeSH-minor] Adolescent. Angiofibroma / diagnosis. Anticonvulsants / therapeutic use. Diagnostic Errors. Epilepsy / drug therapy. Epilepsy / etiology. Female. Humans. Intellectual Disability / etiology. Neurofibromatoses / diagnosis. Skin Neoplasms / diagnosis. Tomography, X-Ray Computed. Treatment Outcome. Valproic Acid / therapeutic use

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  • (PMID = 20587932.001).
  • [ISSN] 0975-5764
  • [Journal-full-title] Annals of African medicine
  • [ISO-abbreviation] Ann Afr Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] Nigeria
  • [Chemical-registry-number] 0 / Anticonvulsants; 614OI1Z5WI / Valproic Acid
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8. Łukomski M, Danilewicz M, Pajor A: [Juvenile angiofibroma in adults]. Otolaryngol Pol; 2008;62(1):20-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Juvenile angiofibroma in adults].
  • INTRODUCTION: Juvenile nasopharyngeal angiofibroma is a benign lesion which is characterized by three distinctive features: it occurs only in one sex, one period of age and in one location in the organism.
  • MATERIAL AND METHOD: Basing on literature and our series concerning 36 patients treated during 50 years, we present atypical cases of angiofibroma.
  • Our study reports three cases of angiofibroma, two of them concerning males aged 34 and 49 years and one case - female aged 68 years.
  • Results of histological examination of our atypical cases were similar as in angiofibromas observed in adolescents.
  • CONCLUSION: Our study concerning the occurrence of juvenile angiofibroma in adults, also in female, as the other observations from literature may constitute some remarks in discussion about the pathogenesis and clinics of this tumor.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Paranasal Sinus Neoplasms / surgery

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  • (PMID = 18637416.001).
  • [ISSN] 0030-6657
  • [Journal-full-title] Otolaryngologia polska = The Polish otolaryngology
  • [ISO-abbreviation] Otolaryngol Pol
  • [Language] pol
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Poland
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9. 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
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  • [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

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  • (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
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10. 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
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  • [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

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  • (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
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11. Starlinger V, Wendler O, Gramann M, Schick B: Laminin expression in juvenile angiofibroma indicates vessel's early developmental stage. Acta Otolaryngol; 2007 Dec;127(12):1310-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Laminin expression in juvenile angiofibroma indicates vessel's early developmental stage.
  • CONCLUSION: This study confirms the wide range of vascular architecture in juvenile angiofibromas.
  • Proof of laminin alpha2 expression in tumour vessels is suggested to indicate presence of vessels of early developmental stage in juvenile angiofibromas, supporting the concept that plexus remnants of the first branchial arch artery contribute to the vascular tumour component.
  • The goal of this study was to analyse the expression of laminins in juvenile angiofibromas.
  • MATERIALS AND METHODS: A detailed analysis of the laminin isoform expression was performed by immunofluorescence staining for laminin chains alpha1, alpha2, alpha3, alpha4, alpha5, beta1, beta2, beta3, gamma1, gamma2, and gamma3 on cryosections of 10 juvenile angiofibromas and inferior nasal turbinate tissue for control.
  • RESULTS: Vascular staining of the different laminin chains revealed areas of differential vessel density in juvenile angiofibromas and irregularities in vessel size, configuration and architecture.
  • Similar to vessels in nasal turbinates, laminins alpha4, alpha5, beta1, beta2 and gamma1 were found to be expressed in juvenile angiofibroma vessels.
  • In contrast to vessels of nasal turbinates, staining for alpha2 and alpha3 chains was only detected in vessels of juvenile angiofibromas.
  • [MeSH-major] Angiofibroma / pathology. Basement Membrane / metabolism. Laminin / metabolism. Nasopharyngeal Neoplasms / pathology

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  • (PMID = 17851944.001).
  • [ISSN] 0001-6489
  • [Journal-full-title] Acta oto-laryngologica
  • [ISO-abbreviation] Acta Otolaryngol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Norway
  • [Chemical-registry-number] 0 / Laminin
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12. Szymańska A, Gołabek W, Siwiec H, Pietura R, Szczerbo-Trojanowska M: [Juvenile angiofibroma: the value of CT and MRI for treatment planning and follow-up]. Otolaryngol Pol; 2005;59(1):85-90
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Juvenile angiofibroma: the value of CT and MRI for treatment planning and follow-up].
  • Juvenile angiofibroma is a rare, benign, hypervascular, nasopharyngeal tumour.
  • There were 40 patients with juvenile angiofibroma.
  • [MeSH-major] Angiofibroma / diagnosis. Magnetic Resonance Angiography. Nasopharyngeal Neoplasms / diagnosis. Tomography, X-Ray Computed

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  • (PMID = 15915924.001).
  • [ISSN] 0030-6657
  • [Journal-full-title] Otolaryngologia polska = The Polish otolaryngology
  • [ISO-abbreviation] Otolaryngol Pol
  • [Language] pol
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Poland
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13. Schick B, Wemmert S, Jung V, Steudel WI, Montenarh M, Urbschat S: Genetic heterogeneity of the MYC oncogene in advanced juvenile angiofibromas. Cancer Genet Cytogenet; 2006 Jan 1;164(1):25-31

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Genetic heterogeneity of the MYC oncogene in advanced juvenile angiofibromas.
  • Despite their benign histological appearance, juvenile angiofibromas sometimes exhibit an aggressive growth behavior.
  • Because intensive cross-talk among beta-catenin, androgen receptor, and C-MYC has been detected recently, we analyzed expression of the C-MYC protooncogene (MYC) on the genetic, transcriptional and translational level in seven sporadic juvenile angiofibromas.
  • Two-color in situ hybridization analyses for chromosome 8 and MYC found in all seven juvenile angiofibromas significant MYC losses.
  • In the three advanced juvenile angiofibromas of this series (Fisch stages III and IV) additional significant MYC gains were observed demonstrating a genetic heterogeneity for the MYC protooncogene.
  • Semiquantitative RT-PCR analyses from laser microdissected endothelial cells and fibroblasts found no differences of C-MYC mRNA levels, leaving open the question of the neoplastic cell in juvenile angiofibromas.
  • The finding of genetic MYC heterogeneity associated with C-MYC overexpression on the mRNA and protein level in advanced juvenile angiofibromas indicates involvement of the MYC oncogene in aggressive growth behavior.
  • [MeSH-major] Angiofibroma / genetics. Genes, myc. Genetic Heterogeneity

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  • (PMID = 16364759.001).
  • [ISSN] 0165-4608
  • [Journal-full-title] Cancer genetics and cytogenetics
  • [ISO-abbreviation] Cancer Genet. Cytogenet.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Proto-Oncogene Proteins c-myc; 0 / RNA, Messenger; 0 / Receptors, Androgen; 0 / Transforming Growth Factor beta; 0 / beta Catenin
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14. El-Banhawy OA, Ragab A, El-Sharnoby MM: Surgical resection of type III juvenile angiofibroma without preoperative embolization. Int J Pediatr Otorhinolaryngol; 2006 Oct;70(10):1715-23

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Surgical resection of type III juvenile angiofibroma without preoperative embolization.
  • OBJECTIVES/HYPOTHESIS: To evaluate the outcome of surgical resection of type III juvenile angiofibroma without preoperative embolizationo in 20 young male patients.
  • PATIENTS AND METHODS: Twenty young male patients with type III JAF (based on Fisch classification by CT/MRI or both), were operated on by endoscopic-assisted midfacial degloving approach without preoperative embolization.
  • Endoscopic transnasal removal of the recurrent JAF was done successfully under local anesthesia in the first patient and under general anesthesia in the second with no recurrence during the follow up period.
  • CONCLUSIONS: Surgical resection of stage III JAF without embolization through endoscopic assisted midfacial degloving approach can be used as an adequate surgical technique with acceptable intraoperative blood loss and low rate of recurrence.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery

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  • (PMID = 16904759.001).
  • [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
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15. Thornton M, Mahesh BN, Lang J: Endoscopic resection of a juvenile angiofibroma: the role of the XPS microdebrider. J Laparoendosc Adv Surg Tech A; 2005 Apr;15(2):194-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Endoscopic resection of a juvenile angiofibroma: the role of the XPS microdebrider.
  • Juvenile angiofibromas are vascular tumors found almost exclusively in the adolescent male.
  • Although benign, their clinical course can be aggressive and can result in major morbidity and mortality.
  • Endoscopic transnasal resection of juvenile angiofibromas, confined to the nose, paranasal sinuses, pterygopalatine fossa, and medial infratemporal fossa, has been a significant advance in their management, eliminating or reducing the need for extensive soft tissue and bony dissection of traditional surgical approaches.
  • We discuss a case of a juvenile angiofibroma resected transnasally using the XPS microdebrider (Medtonic Xomed, Jacksonville, Florida) and outline the role of this instrument in this surgery.
  • [MeSH-major] Angiofibroma / surgery. Debridement / instrumentation. Endoscopy / methods. Head and Neck Neoplasms / surgery

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  • (PMID = 15898917.001).
  • [ISSN] 1092-6429
  • [Journal-full-title] Journal of laparoendoscopic & advanced surgical techniques. Part A
  • [ISO-abbreviation] J Laparoendosc Adv Surg Tech A
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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16. Tyagi I, Syal R, Goyal A: Recurrent and residual juvenile angiofibromas. J Laryngol Otol; 2007 May;121(5):460-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Recurrent and residual juvenile angiofibromas.
  • INTRODUCTION: In the surgical management of juvenile nasopharyngeal angiofibromas the possibility of recurrences and residual tumours is always there.
  • This study was undertaken to predict the prognostic factors determining recurrence of juvenile nasopharyngeal angiofibroma and to find out the usual sites of these tumours.
  • MATERIAL AND METHODS: The medical records of 95 patients with histologically proven juvenile nasopharyngeal angiofibroma were reviewed retrospectively.
  • RESULTS: Complete removal of the juvenile nasopharyngeal angiofibroma was achieved in 78 (82 per cent) of the cases in a single operation.
  • CONCLUSIONS: Extensions into the pterygoid fossa and basisphenoid, erosion of the clivus, intracranial extensions medial to the cavernous sinus, invasion of the sphenoid diploe through a widened pterygoid canal, feeders from the internal carotid artery, a young age and a residual tumour were risk factors found associated with recurrence of juvenile nasopharyngeal angiofibroma.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Neoplasm Recurrence, Local

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  • (PMID = 17210091.001).
  • [ISSN] 1748-5460
  • [Journal-full-title] The Journal of laryngology and otology
  • [ISO-abbreviation] J Laryngol Otol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
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17. Padilla Parrado M, Díaz Sastre MA, Jiménez Antolín JA, Caro García MA: [Juvenile nasopharyngeal angiofibroma]. An Otorrinolaringol Ibero Am; 2005;32(4):361-71

  • [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

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  • (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
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18. 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

  • [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

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  • (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
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19. Thuesen AD, Jakobsen J, Nepper-Rasmussen J: [Treatment of juvenile angiofibroma with particle embolization and endoscopic surgery]. Ugeskr Laeger; 2005 Aug 22;167(34):3167-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Treatment of juvenile angiofibroma with particle embolization and endoscopic surgery].
  • [Transliterated title] Behandling af juvenile angiofibromer med partikelembolisering og endoskopisk kirurgi.
  • INTRODUCTION: Juvenile angiofibroma is a benign, rich vascular nasal tumor, and the biggest complication in surgery is the great loss of blood.
  • DISCUSSION: Endovascular embolization of juvenile angiofibromas followed by endoscopic surgery is considered to be the preferred treatment method today.
  • [MeSH-major] Angiofibroma / therapy. Embolization, Therapeutic / methods. Nasopharyngeal Neoplasms / therapy

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  • [CommentIn] Ugeskr Laeger. 2005 Nov 21;167(47):4482 [16305784.001]
  • (PMID = 16117915.001).
  • [ISSN] 1603-6824
  • [Journal-full-title] Ugeskrift for laeger
  • [ISO-abbreviation] Ugeskr. Laeg.
  • [Language] dan
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Denmark
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20. Gramann M, Wendler O, Haeberle L, Schick B: Prominent collagen type VI expression in juvenile angiofibromas. Histochem Cell Biol; 2009 Jan;131(1):155-64

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Prominent collagen type VI expression in juvenile angiofibromas.
  • Although, juvenile angiofibromas (JAs) often exhibit an aggressive growth pattern, the collagen type VI expression of this fibrovascular tumour has not been addressed so far.
  • [MeSH-major] Angiofibroma / metabolism. Collagen Type VI / metabolism

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  • (PMID = 18797915.001).
  • [ISSN] 1432-119X
  • [Journal-full-title] Histochemistry and cell biology
  • [ISO-abbreviation] Histochem. Cell Biol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Collagen Type VI
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21. Schick B, Wemmert S, Bechtel U, Nicolai P, Hofmann T, Golabek W, Urbschat S: Comprehensive genomic analysis identifies MDM2 and AURKA as novel amplified genes in juvenile angiofibromas. Head Neck; 2007 May;29(5):479-87
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Comprehensive genomic analysis identifies MDM2 and AURKA as novel amplified genes in juvenile angiofibromas.
  • BACKGROUND: Frequent beta-catenin mutations have been detected in juvenile angiofibromas, but the tumor pathogenesis remains unknown.
  • CONCLUSION: Metaphase-CGH results confirmed numerous chromosomal aberrations in juvenile angiofibromas.
  • AURKA and MDM2 were identified as interesting novel amplified genes in juvenile angiofibromas.
  • [MeSH-major] Angiofibroma / genetics. Chromosome Aberrations. Head and Neck Neoplasms / genetics. Protein-Serine-Threonine Kinases / genetics. Proto-Oncogene Proteins c-mdm2 / genetics

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  • [Copyright] (c) 2006 Wiley Periodicals, Inc.
  • (PMID = 17120309.001).
  • [ISSN] 1043-3074
  • [Journal-full-title] Head & neck
  • [ISO-abbreviation] Head Neck
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] EC 2.7.11.1 / AURKA protein, human; EC 2.7.11.1 / Aurora Kinase A; EC 2.7.11.1 / Aurora Kinases; EC 2.7.11.1 / Protein-Serine-Threonine Kinases; EC 6.3.2.19 / MDM2 protein, human; EC 6.3.2.19 / Proto-Oncogene Proteins c-mdm2
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22. Thuesen AD, Jakobsen J, Nepper-Rasmussen J: [Juvenile angiofibroma]. Ugeskr Laeger; 2005 Aug 22;167(34):3163-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Juvenile angiofibroma].
  • [Transliterated title] Juvenile angiofibromer.
  • Juvenile angiofibroma is a rare, benign, rich vascular tumor, and approximately one new case is diagnosed in Denmark each year.
  • Through the years, the treatment of juvenile angiofibroma has included many methods, including surgical excision, electrocoagulation, interstitial or external radiation therapy, cryosurgery, hormone administration and chemotherapy.
  • [MeSH-major] Angiofibroma. Nasopharyngeal Neoplasms

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  • [CommentIn] Ugeskr Laeger. 2005 Nov 21;167(47):4482 [16305784.001]
  • (PMID = 16117914.001).
  • [ISSN] 1603-6824
  • [Journal-full-title] Ugeskrift for laeger
  • [ISO-abbreviation] Ugeskr. Laeg.
  • [Language] dan
  • [Publication-type] English Abstract; Journal Article; Review
  • [Publication-country] Denmark
  • [Number-of-references] 25
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23. Pradhan B, Thapa N: Juvenile angiofibroma and its management. Nepal Med Coll J; 2009 Sep;11(3):186-8

  • [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

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  • (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
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24. 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

  • [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

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  • (PMID = 16775738.001).
  • [ISSN] 1433-0458
  • [Journal-full-title] HNO
  • [ISO-abbreviation] HNO
  • [Language] ger
  • [Publication-type] Clinical Trial; Journal Article
  • [Publication-country] Germany
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25. Kapidzić A, Sutalo K: [Surgical treatment of juvenile nasopharyngeal angifibroma]. Med Arh; 2006;60(5):296-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Surgical treatment of juvenile nasopharyngeal angifibroma].
  • [Transliterated title] Operativno lijecenje juvenilnog nazofaringealnog angiofibroma.
  • Juvenile nasopharyngeal angiofibroma represents non-incapsulated benign tumor.
  • Three patients with juvenile nasopharyngeal angiofibroma that underwent surgery in a five year period (2001-2005) at the ENT Clinic of the University Clinical Center in Sarajevo are evaluated in this paper.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery

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  • (PMID = 16944730.001).
  • [Journal-full-title] Medicinski arhiv
  • [ISO-abbreviation] Med Arh
  • [Language] bos
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Bosnia and Herzegovina
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26. Wendler O, Schäfer R, Schick B: Mast cells and T-lymphocytes in juvenile angiofibromas. Eur Arch Otorhinolaryngol; 2007 Jul;264(7):769-75
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Mast cells and T-lymphocytes in juvenile angiofibromas.
  • Juvenile angiofibroma (JA) is regarded as a benign fibrovascular tumour of unknown aetiology.
  • Due to its fibrovascular architecture the fibrous and vascular tumour component have been in the focus of most studies.
  • Western blot analysis supported finding of remarkable expression of the mast cell markers tryptase and chymase in JAs and indicated for both proteins similar but also different molecular weights than being observed in NM.
  • Regarding these observations JAs are certainly not only built up by vascular cells and fibrous stroma cells.
  • [MeSH-major] Angiofibroma / pathology. CD4-Positive T-Lymphocytes / pathology. CD8-Positive T-Lymphocytes / pathology. Mast Cells / pathology. Nose Neoplasms / pathology

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  • (PMID = 17310347.001).
  • [ISSN] 0937-4477
  • [Journal-full-title] European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
  • [ISO-abbreviation] Eur Arch Otorhinolaryngol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; EC 3.4.21.39 / Chymases; EC 3.4.21.59 / Tryptases
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27. Tosun F, Onerci M, Durmaz A, Ugurel S: Spontaneous involution of nasopharyngeal angiofibroma. J Craniofac Surg; 2008 Nov;19(6):1686-9

  • [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

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  • (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
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28. Cherekaev VA, Gol'bin DA, Kapitanov DN, Belov AI, Arustamian SR, Gromova VV, Imaev AA: [Surgical treatment of extensive craniofacial juvenile angiofibromas]. Zh Vopr Neirokhir Im N N Burdenko; 2009 Apr-Jun;(2):9-14; discussion 14-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Surgical treatment of extensive craniofacial juvenile angiofibromas].
  • Juvenile nasopharyngeal angiofibroma (JNA) is a rare benign tumor occurring almost exclusively in adolescent and young adult males.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Otorhinolaryngologic Surgical Procedures / methods

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  • (PMID = 19569543.001).
  • [ISSN] 0042-8817
  • [Journal-full-title] Zhurnal voprosy neĭrokhirurgii imeni N. N. Burdenko
  • [ISO-abbreviation] Zh Vopr Neirokhir Im N N Burdenko
  • [Language] rus
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Russia (Federation)
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29. 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

  • [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

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  • (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)
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30. Falkner JA, Falkner JW, Andrews PC: ProteomeCommons.org JAF: reference information and tools for proteomics. Bioinformatics; 2006 Mar 1;22(5):632-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] ProteomeCommons.org JAF: reference information and tools for proteomics.
  • The Java Analysis Framework (JAF) for proteomics provides a freely usable, open-source library of Java code that abstracts all of the aforementioned data, enabling more rapid development of proteomics tools.
  • The JAF also includes several user tools that can be run directly from a web browser.

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  • (PMID = 16434446.001).
  • [ISSN] 1367-4803
  • [Journal-full-title] Bioinformatics (Oxford, England)
  • [ISO-abbreviation] Bioinformatics
  • [Language] eng
  • [Grant] United States / NCRR NIH HHS / RR / P41-RR018627
  • [Publication-type] Journal Article; Research Support, N.I.H., Extramural
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Proteins
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31. 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
MedlinePlus Health Information. consumer health - Nasal Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] 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

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  • (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
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32. 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
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  • [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

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  • (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
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33. Celik B, Erisen L, Saraydaroglu O, Coskun H: Atypical angiofibromas: a report of four cases. Int J Pediatr Otorhinolaryngol; 2005 Mar;69(3):415-21
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Atypical angiofibromas: a report of four cases.
  • In this study, our four patients with angiofibroma with various atypical features are presented.
  • 14 patients, diagnosed and treated for angiofibroma in the Otorhinolaryngology Department of Faculty of Medicine in Uludag University between January 1992 and December 2003, have been evaluated.
  • Angiofibromas presenting with at least one of the following criteria such as origin or location other than nasopharynx, presenting complaints other than nasal obstruction or epistaxis, aged younger than seven or older than 25, female sex, atypical histopathology and multifocalitiy were considered as "atypical".
  • Four of 14 angiofibromas (28.5%), which were diagnosed and treated in our clinic, had atypical features.
  • The patients, who have different characteristics other than classical angiofibromas, may be called "Atypical Angiofibroma (AAF)", under the scope of the related literature and our experience.
  • [MeSH-major] Angiofibroma / pathology. Cheek / pathology. Nasopharyngeal Neoplasms / pathology. Nose Neoplasms / pathology. Soft Tissue Neoplasms / pathology. Tonsillar Neoplasms / pathology. Turbinates / pathology

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  • (PMID = 15733604.001).
  • [ISSN] 0165-5876
  • [Journal-full-title] International journal of pediatric otorhinolaryngology
  • [ISO-abbreviation] Int. J. Pediatr. Otorhinolaryngol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Ireland
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34. Duerr S, Wendler O, Aigner T, Karosi S, Schick B: Metalloproteinases in juvenile angiofibroma--a collagen rich tumor. Hum Pathol; 2008 Feb;39(2):259-68
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Metalloproteinases in juvenile angiofibroma--a collagen rich tumor.
  • MMPs with gelatinase/collagenase activity have not yet been studied in juvenile angiofibroma, a unique fibrovascular tumor with prominent collagen expression.
  • Quantitative real-time polymerase chain reaction studies, Western blot analysis, immunofluorescence studies, gel zymography, and in situ zymography were used to analyze MMP-1, MMP-2, MMP-9, MMP-13, MMP-14, TIMP-1, and TIMP-2 in 9 juvenile angiofibromas and 2 inferior nasal turbinate specimens.
  • Western blot analysis detected more prominent MMP-1, MMP-2, and MMP-9 protein levels in juvenile angiofibromas compared with inferior nasal turbinates, but not MMP-13, MMP-14, TIMP-1, and TIMP-2.
  • Gel zymography indicated increased MMP-2 and MMP-9 gelatinase activity in juvenile angiofibromas compared with inferior nasal turbinates.
  • This study indicates significant expression of MMPs with gelatinase/collagenase activity in juvenile angiofibromas with evidence of a disturbed balance of MMPs to TIMPs toward enhanced MMP activity.
  • [MeSH-major] Angiofibroma / enzymology. Biomarkers, Tumor / metabolism. Collagen / metabolism. Metalloproteases / metabolism. Nose Neoplasms / enzymology

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  • (PMID = 17950779.001).
  • [ISSN] 0046-8177
  • [Journal-full-title] Human pathology
  • [ISO-abbreviation] Hum. 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 / RNA, Messenger; 0 / RNA, Neoplasm; 0 / Tissue Inhibitor of Metalloproteinase-1; 127497-59-0 / Tissue Inhibitor of Metalloproteinase-2; 9007-34-5 / Collagen; EC 3.4.- / Metalloproteases
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35. Yi ZX, Li ZC, Cheng JM, Zhang R, Lin C, Zhou AD, Fan ZM: Huge nasopharyngeal angiofibroma with intracranial extension: change in the dura mater and choice of surgical management. J Laryngol Otol; 2007 Nov;121(11):1108-12

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Huge nasopharyngeal angiofibroma with intracranial extension: change in the dura mater and choice of surgical management.
  • We aimed to review (1) the imaging changes in the dura mater in cases of huge, lobulated juvenile nasopharyngeal angiofibroma, and (2) the choice of surgical management.
  • Imaging from four cases of juvenile nasopharyngeal angiofibroma showed extrapharyngeal extension of the tumour.
  • [MeSH-major] Angiofibroma / pathology. Dura Mater / radiography. Nasopharyngeal Neoplasms / pathology. Otorhinolaryngologic Surgical Procedures / methods

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  • (PMID = 17295934.001).
  • [ISSN] 1748-5460
  • [Journal-full-title] The Journal of laryngology and otology
  • [ISO-abbreviation] J Laryngol Otol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] England
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36. Sennes LU, Fortes FS, Butugan O, Saldiva PH, Bernardi FC: Tissue maturation correlating to clinical manifestations in juvenile angiofibroma. Ann Otol Rhinol Laryngol; 2005 Sep;114(9):705-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Tissue maturation correlating to clinical manifestations in juvenile angiofibroma.
  • OBJECTIVES: Juvenile nasopharyngeal angiofibroma is a rare benign tumor that affects young male patients and shows a characteristic development from its origin.
  • It is not a true neoplasm, but shows features of vascular processes, developing into a more fibrous condition.
  • [MeSH-major] Angiofibroma / pathology. Nasopharyngeal Neoplasms / pathology

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  • (PMID = 16240934.001).
  • [ISSN] 0003-4894
  • [Journal-full-title] The Annals of otology, rhinology, and laryngology
  • [ISO-abbreviation] Ann. Otol. Rhinol. Laryngol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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37. Bleier BS, Kennedy DW, Palmer JN, Chiu AG, Bloom JD, O'Malley BW Jr: Current management of juvenile nasopharyngeal angiofibroma: a tertiary center experience 1999-2007. Am J Rhinol Allergy; 2009 May-Jun;23(3):328-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Current management of juvenile nasopharyngeal angiofibroma: a tertiary center experience 1999-2007.
  • BACKGROUND: Over the past 10 years, the management of juvenile nasopharyngeal angiofibroma (JNA) has been redefined because of the improvement of transnasal skull base techniques.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery

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  • (PMID = 19490810.001).
  • [ISSN] 1945-8924
  • [Journal-full-title] American journal of rhinology & allergy
  • [ISO-abbreviation] Am J Rhinol Allergy
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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38. 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
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  • [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

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  • (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
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39. Chistiakova VR, Poliaev IuA, Kovshenkova IuD, Vasil'eva NI, Myl'nikov AA, Pronin AE: [Hemostatic provision of surgical treatment of juvenile angiofibromas of the skull base in children]. Vestn Otorinolaringol; 2006;(1):24-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Hemostatic provision of surgical treatment of juvenile angiofibromas of the skull base in children].
  • For three years we operated sixty two 7-16-year-old children for angiofibroma of the base of the skull.
  • Neither lethal outcomes nor complications occurred in children during removal of angiofibromas of the base of the skull.
  • [MeSH-major] Angiofibroma / surgery. Blood Loss, Surgical / prevention & control. Hemostatic Techniques. Hemostatics / therapeutic use. Postoperative Hemorrhage / prevention & control. Skull Base Neoplasms / surgery

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  • (PMID = 16482005.001).
  • [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)
  • [Chemical-registry-number] 0 / Hemostatics
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40. Bansal C, Stewart D, Li A, Cockerell CJ: Histologic variants of fibrous papule. J Cutan Pathol; 2005 Jul;32(6):424-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Histologic variants of fibrous papule.
  • Fibrous papules (FPs) are common benign lesions usually of the face.
  • [MeSH-major] Angiofibroma / pathology. Facial Neoplasms / pathology. Skin Neoplasms / pathology

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  • (PMID = 15953376.001).
  • [ISSN] 0303-6987
  • [Journal-full-title] Journal of cutaneous pathology
  • [ISO-abbreviation] J. Cutan. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Denmark
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41. 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
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  • [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.

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  • (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
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42. Kösling S, Knipping S, Hofmockel T: [Imaging of nasopharyngeal diseases]. HNO; 2009 Aug;57(8):813-24; quiz 825
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  • [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] Image Enhancement / methods. Magnetic Resonance Imaging / methods. Nasopharyngeal Diseases / diagnosis. Nasopharynx / diagnostic imaging. Nasopharynx / pathology. Tomography, X-Ray Computed / methods

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  • [Cites] Br J Radiol. 2007 Jul;80(955):e145-6 [17704311.001]
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  • (PMID = 19639275.001).
  • [ISSN] 1433-0458
  • [Journal-full-title] HNO
  • [ISO-abbreviation] HNO
  • [Language] ger
  • [Publication-type] Journal Article; Review
  • [Publication-country] Germany
  • [Number-of-references] 21
  •  go-up   go-down


43. 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
MedlinePlus Health Information. consumer health - Nasal Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • 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.

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  • (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
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44. Septer S, Thompson ES, Willemsen-Dunlap A: Anesthesia concerns for children with tuberous sclerosis. AANA J; 2006 Jun;74(3):219-25
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • We describe a 10-year-old girl with TS scheduled to receive a general anesthetic for laser treatment of facial angiofibromas.
  • The patient had several coexisting maladies from TS, including hypertension, autism, seizure disorder, cardiac rhabdomyomas, developmental delay, and bilateral polycystic renal disease.
  • [MeSH-minor] Angiofibroma / etiology. Angiofibroma / surgery. Child. Developmental Disabilities / etiology. Echocardiography. Facial Neoplasms / etiology. Facial Neoplasms / surgery. Female. Genes, Dominant / genetics. Heart Neoplasms / etiology. Heart Neoplasms / ultrasonography. Humans. Hypertension / etiology. Incidence. Laser Therapy. Nursing Assessment. Patient Care Planning. Penetrance. Perioperative Care / methods. Perioperative Care / nursing. Polycystic Kidney Diseases / etiology. Rare Diseases. Rhabdomyoma / etiology. Rhabdomyoma / ultrasonography. Seizures / etiology

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  • (PMID = 16786916.001).
  • [ISSN] 0094-6354
  • [Journal-full-title] AANA journal
  • [ISO-abbreviation] AANA J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 50
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45. Erkan AN, Tarhan E, Yilmazer C, Cağici A, Cakmak O: [Endoscopic removal of sinonasal tumors]. Kulak Burun Bogaz Ihtis Derg; 2006;16(2):72-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • RESULTS: There were five osteomas, one fibrous dysplasia, one ossifying fibroma, seven inverted papillomas, one oncocytic papilloma, three angiofibromas, one schwannoma, and one esthesioneuroblastoma.
  • The fibrous dysplasia involving the posterior ethmoid sinuses was subtotally resected due to its close proximity to the optic nerve.
  • [MeSH-minor] Adolescent. Adult. Child. Endoscopy / utilization. Female. Fibroma / epidemiology. Fibroma / etiology. Fibroma / pathology. Fibroma / surgery. Humans. Male. Medical Records. Middle Aged. Neurilemmoma / epidemiology. Neurilemmoma / etiology. Neurilemmoma / pathology. Neurilemmoma / surgery. Osteoma / epidemiology. Osteoma / etiology. Osteoma / pathology. Osteoma / surgery. Papilloma / epidemiology. Papilloma / etiology. Papilloma / pathology. Papilloma / surgery. Retrospective Studies. Turkey / epidemiology

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  • (PMID = 16763420.001).
  • [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
  • [Publication-country] Turkey
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46. Lehmann M, Ulrich S, Reineke U, Hamberger U, Dietrich U, Sudhoff H: [Intratumoral Onyx embolisation in the management of juvenile nasopharyngeal angiofibroma]. HNO; 2010 Aug;58(8):853-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Intratumoral Onyx embolisation in the management of juvenile nasopharyngeal angiofibroma].
  • Preoperative embolization for the treatment of juvenile nasopharyngeal angiofibroma was successfully accomplished with Onyx by intratumoral puncture for the first time.
  • Transnasal surgery on the following day achieved complete resection of the angiofibroma without complications.
  • Direct intratumoral embolization of juvenile nasopharyngeal angiofibromas appears to be a safe and effective preoperative method without complications.
  • [MeSH-major] Angiofibroma / blood supply. Angiofibroma / surgery. Dimethyl Sulfoxide. Embolization, Therapeutic / methods. Nasopharyngeal Neoplasms / blood supply. Nasopharyngeal Neoplasms / surgery. Polyvinyls. Preoperative Care

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  • (PMID = 20596683.001).
  • [ISSN] 1433-0458
  • [Journal-full-title] HNO
  • [ISO-abbreviation] HNO
  • [Language] ger
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Onyx copolymer; 0 / Polyvinyls; YOW8V9698H / Dimethyl Sulfoxide
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47. 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

  • [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

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  • (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
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48. Val-Bernal JF, Rubio S, Garijo MF, González-Vela MC: Extragenital subcutaneous cellular angiofibroma. Case report. APMIS; 2007 Mar;115(3):254-8
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  • [Title] Extragenital subcutaneous cellular angiofibroma. Case report.
  • Cellular angiofibroma (CAF) is a rare distinctive mesenchymal neoplasm that occurs almost exclusively in the genital area.
  • We report the case of a 38-year-old woman who presented with an asymptomatic subcutaneous mass, 3.5 cm in diameter, located in the left hypochondrium, which had progressively enlarged during the previous 6 months.
  • [MeSH-major] Angiofibroma / pathology. Angiofibroma / surgery. Skin Neoplasms / pathology

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  • (PMID = 17367472.001).
  • [ISSN] 0903-4641
  • [Journal-full-title] APMIS : acta pathologica, microbiologica, et immunologica Scandinavica
  • [ISO-abbreviation] APMIS
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
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49. Hosseini SM, Borghei P, Borghei SH, Ashtiani MT, Shirkhoda A: Angiofibroma: an outcome review of conventional surgical approaches. Eur Arch Otorhinolaryngol; 2005 Oct;262(10):807-12

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Angiofibroma: an outcome review of conventional surgical approaches.
  • Juvenile nasopharyngeal angiofibroma (JNA) is a benign tumor of the nasopharynx, and for its treatment, many surgical approaches have been recommended.
  • Three of them were disease free, and in two cases residues were demonstrated that were asymptomatic and were chosen only to be observed.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Neoplasm Recurrence, Local / epidemiology. Otorhinolaryngologic Surgical Procedures / methods
  • [MeSH-minor] Adolescent. Adult. Child. Disease-Free Survival. Follow-Up Studies. Humans. Magnetic Resonance Imaging. Male. Neoplasm Invasiveness. Neoplasm Staging. Retrospective Studies. Tomography, X-Ray Computed. Treatment Outcome

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  • (PMID = 15739087.001).
  • [ISSN] 0937-4477
  • [Journal-full-title] European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
  • [ISO-abbreviation] Eur Arch Otorhinolaryngol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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50. 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
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  • [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

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  • (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
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51. Shunyu NB, Thakar A, Gupta V: Complete resolution of stage IIIB juvenile nasopharyngeal angiofibroma with radiation therapy. Indian J Otolaryngol Head Neck Surg; 2008 Sep;60(3):238-41

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Complete resolution of stage IIIB juvenile nasopharyngeal angiofibroma with radiation therapy.
  • Juvenile nasopharyngeal angiofibroma is a benign, locally aggressive, vascular tumour of adolescent males.
  • Hence we are re-affirming the earlier studies than angiofibroma mass regresses gradually after completion of radiotherapy.
  • Radiotherapy is a useful way of treating angiofibroma with significant intracranial extension.

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  • [Cites] Head Neck Surg. 1979 Nov-Dec;2(2):119-28 [233745.001]
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  • (PMID = 23120551.001).
  • [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/ PMC3450647
  • [Keywords] NOTNLM ; Angiofibroma / Intracranial extension / Radiotherapy
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52. Lin C, Li ZC, Cheng JM, Lin GB, Zhou AD, Yi ZX: [Pathological features and clinical managements of nasopharyngeal angiofibroma]. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2008 Oct;43(10):763-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Pathological features and clinical managements of nasopharyngeal angiofibroma].
  • OBJECTIVE: To study the pathological features of nasopharyngeal angiofibroma (NA) and the principles for clinical managements.
  • The tumor extensions such as in pterygopalatine fossa and infratemporal fossa were covered by fibrous pseudocapsule.
  • CONCLUSIONS: nasopharyngeal angiofibroma is covered by epithelium or pseudo-capsule, it does not infiltrate the surrounding tissue.
  • [MeSH-major] Angiofibroma / pathology. Nasopharyngeal Neoplasms / pathology

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  • (PMID = 19119673.001).
  • [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; Journal Article
  • [Publication-country] China
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53. 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
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  • [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

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  • (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
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54. Sciarretta V, Pasquini E, Farneti G, Frank G, Mazzatenta D, Calbucci F: Endoscopic sinus surgery for the treatment of vascular tumors. Am J Rhinol; 2006 Jul-Aug;20(4):426-31
MedlinePlus Health Information. consumer health - Nasal Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: This study points out the effectiveness of the endoscopic approach for the treatment of vascular lesions such as angiofibroma, hemangioma, and hemangiopericytoma involving the nose and paranasal sinuses.
  • RESULTS: The follow-up of this series varied from 6 to 75 months (mean, 23 months); only one recurrence (8%) was observed in the juvenile angiofibroma group encountered 20 months postoperatively.
  • The average intraoperative blood loss for the removal of the juvenile angiofibroma group was 300 mL and it was 100 mL for the other vascular tumors.
  • Even in the presence of a lesion with limited intracranial extension, the tumor still may be amenable to an endoscopic approach alone.

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  • (PMID = 16955773.001).
  • [ISSN] 1050-6586
  • [Journal-full-title] American journal of rhinology
  • [ISO-abbreviation] Am J Rhinol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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55. Onerci M, Oğretmenoğlu O, Yücel T: Juvenile nasopharyngeal angiofibroma: a revised staging system. Rhinology; 2006 Mar;44(1):39-45

  • [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

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  • (PMID = 16550949.001).
  • [ISSN] 0300-0729
  • [Journal-full-title] Rhinology
  • [ISO-abbreviation] Rhinology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
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56. Durko M, Murlewska A, Gryczyński M, Ratyńska M, Pietruszewska W: [Angiofibroma of the nasal cavity and anterior ethmoid cells--problems in differential diagnosis]. Otolaryngol Pol; 2007;61(5):736-9
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  • [Title] [Angiofibroma of the nasal cavity and anterior ethmoid cells--problems in differential diagnosis].
  • [Transliterated title] Angiofibroma jamy nosa i komórek sitowych przednich u kobiety--problemy diagnostyki róznicowej.
  • BACKGROUND: Nasal angiofibromas are commonly called juvenile nasal angiofibromas (JNA) because of the almost exclusive occurrence in adolescent males.
  • It is a relatively rare benign fibrovascular tumor originating in the posterior lateral wall of the nasopharynx with only a very few cases diagnosed in females.
  • CASE REPORT: Authors present a case of a 26 y.o. woman with JNA in left nasal cavity with extension to the anterior left ethmoid cells diagnosed and surgically treated at the ENT Department, Medical University of Lodz.
  • CONCLUSION: Although angiofibroma in females is an extremely rare tumor of a sinonasal tract it should be taken into consideration in the differential diagnosis of all nasal cavity tumors (especially solitary fibrous tumor).
  • [MeSH-major] Angiofibroma / pathology. Ethmoid Sinus / pathology. Nose Neoplasms / pathology

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  • (PMID = 18552009.001).
  • [ISSN] 0030-6657
  • [Journal-full-title] Otolaryngologia polska = The Polish otolaryngology
  • [ISO-abbreviation] Otolaryngol Pol
  • [Language] pol
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Poland
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57. Rong Z, Zixiang Y, Chang L, Guoxing X, Sheng Z, Yuanteng X, Zheming F, Zhihong C: Lacrimal hyposecretion: a surgical complication of juvenile nasopharyngeal angiofibroma. Am J Otolaryngol; 2008 Nov-Dec;29(6):367-71

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Lacrimal hyposecretion: a surgical complication of juvenile nasopharyngeal angiofibroma.
  • PURPOSE: The aim of this study was to evaluate lacrimal hyposecretion in the surgical management of juvenile nasopharyngeal angiofibroma (JNA) and discuss how to prevent and treat this expected surgical complication.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Otorhinolaryngologic Surgical Procedures / adverse effects. Xerophthalmia / etiology

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  • (PMID = 19144296.001).
  • [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
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58. 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
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  • [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


59. 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

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  • [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

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  • (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
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60. Mistry RC, Qureshi SS, Gupta S, Gupta S: Juvenile nasopharyngeal angiofibroma: a single institution study. Indian J Cancer; 2005 Jan-Mar;42(1):35-9

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Juvenile nasopharyngeal angiofibroma: a single institution study.
  • BACKGROUND: Juvenile nasopharyngeal angiofibroma (JNA) is a rare tumor of adolescent males and there is a paucity of Indian studies on this subject.
  • The age distribution, disease patterns, management approaches and treatment outcomes of patients in the two groups were recorded.
  • RESULTS: The mean age at presentation was 16 years and more than 90% of the patients had Stage III or IV disease.
  • Aggressive re-resection should be done for resectable recurrences reserving radiotherapy for unresectable, recurrent/ residual disease.
  • [MeSH-major] Angiofibroma / epidemiology. Nasopharyngeal Neoplasms / epidemiology. Neoplasm Recurrence, Local / epidemiology

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  • (PMID = 15805690.001).
  • [ISSN] 0019-509X
  • [Journal-full-title] Indian journal of cancer
  • [ISO-abbreviation] Indian J Cancer
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
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61. Cherekaev VA, Belov AI, Kulikovskiĭ PV, Arustamian SR: [Juvenile angiofibroma predominantly extending into the middle cranial fossa and eye-socket]. Zh Vopr Neirokhir Im N N Burdenko; 2006 Jan-Mar;(1):37-9; discussion 39-40

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Juvenile angiofibroma predominantly extending into the middle cranial fossa and eye-socket].
  • The paper analyzes a rare case of juvenile angiofibroma primarily locating in the infratemporal and middle cranial fossa without a nodule in the nasopharynx.
  • Since the disease has started from right facial hypesthesia, neurinoma involving the first and second branches of the trigeminal nerve and spreading to the eye-socket may be suggested.
  • [MeSH-major] Angiofibroma / diagnosis. Angiofibroma / surgery. Skull Base Neoplasms / diagnosis. Skull Base Neoplasms / surgery

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  • (PMID = 16739934.001).
  • [ISSN] 0042-8817
  • [Journal-full-title] Zhurnal voprosy neĭrokhirurgii imeni N. N. Burdenko
  • [ISO-abbreviation] Zh Vopr Neirokhir Im N N Burdenko
  • [Language] rus
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Russia (Federation)
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62. Ngan BY, Forte V, Campisi P: Molecular angiogenic signaling in angiofibromas after embolization: implications for therapy. Arch Otolaryngol Head Neck Surg; 2008 Nov;134(11):1170-6
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  • [Title] Molecular angiogenic signaling in angiofibromas after embolization: implications for therapy.
  • OBJECTIVES: To examine (1) the molecular angiogenic relationship between endothelial and stromal cells of angiofibromas and how this may elucidate the pathogenesis of angiofibromas and (2) the effects of embolization on the expression of angiotrophic factors and proapoptotic and antiapoptotic factors within the tumor.
  • DESIGN: The expression of mesenchymal and endothelial stem/progenitor cell-associated proteins (MECAPs) such as proangiogenic cytokine vascular endothelial growth factor (VEGF), VEGF receptors (VEGFR1, VEGFR2, and VEGFR3), angiopoietin receptors (Tie-1 and Tie-2), and stem cell subset marker CD133 was assessed by immunohistological staining in 7 embolized angiofibroma specimens.
  • Expression of proapoptotic Bax, antiapoptotic Bcl-2 and Bcl-xL, nuclear proliferation protein MiB-1, and hypoxia-inducible factor 1alpha (Hif-1alpha) in peri-ischemic areas of the embolized angiofibromas was also assessed.
  • PATIENTS: Seven patients (identified from medical records, January 1, 2001, through December 31, 2005) who were diagnosed as having juvenile angiofibroma and who underwent surgical treatment.
  • RESULTS: All angiofibroma specimens expressed the stem cell subset marker CD133 and MECAPs except VEGFR3 (a few cases).
  • Specific angiogenesis blockers may represent a novel treatment strategy for angiofibromas.
  • [MeSH-major] Angiofibroma / genetics. Angiofibroma / therapy. Biomarkers, Tumor / genetics. Embolization, Therapeutic. Neoplasm Proteins / genetics. Otorhinolaryngologic Neoplasms / genetics. Otorhinolaryngologic Neoplasms / therapy. Signal Transduction / genetics

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  • (PMID = 19015446.001).
  • [ISSN] 1538-361X
  • [Journal-full-title] Archives of otolaryngology--head & neck surgery
  • [ISO-abbreviation] Arch. Otolaryngol. Head Neck Surg.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Angiogenesis Inducing Agents; 0 / Biomarkers, Tumor; 0 / HIF1A protein, human; 0 / Hypoxia-Inducible Factor 1, alpha Subunit; 0 / Neoplasm Proteins; 0 / Vascular Endothelial Growth Factor A
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63. Gallia GL, Ramanathan M Jr, Blitz AM, Reh DD: Expanded endonasal endoscopic approach for resection of a juvenile nasopharyngeal angiofibroma with skull base involvement. J Clin Neurosci; 2010 Nov;17(11):1423-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Expanded endonasal endoscopic approach for resection of a juvenile nasopharyngeal angiofibroma with skull base involvement.
  • Juvenile nasopharyngeal angiofibromas (JNAs) are rare vascular tumors which arise in the nasopharynx of adolescent males.
  • In this report, we describe a patient with a JNA with skull base involvement who underwent an expanded endonasal endoscopic approach for a complete resection.
  • [MeSH-major] Angiofibroma / surgery. Endoscopy / methods. Nasal Cavity / surgery. Nasopharyngeal Neoplasms / surgery. Nasopharynx / surgery. Skull Base Neoplasms / surgery

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  • [Copyright] Copyright © 2010 Elsevier Ltd. All rights reserved.
  • (PMID = 20708935.001).
  • [ISSN] 1532-2653
  • [Journal-full-title] Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
  • [ISO-abbreviation] J Clin Neurosci
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Scotland
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64. 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
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  • [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

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  • (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
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65. Rzaev RM: [The role of angiography in diagnosis and surgical treatment of patients with juvenile angiofibroma of the nasopharynx]. Vestn Otorinolaringol; 2007;(4):18-22

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [The role of angiography in diagnosis and surgical treatment of patients with juvenile angiofibroma of the nasopharynx].
  • 22 of them had juvenile nasopharyngeal angiofibroma (JNA), 8 patients had early cancer.
  • [MeSH-major] Angiofibroma / diagnosis. Angiofibroma / surgery. Angiography / methods. Carotid Arteries / radiography. Nasopharyngeal Neoplasms / diagnosis. Nasopharyngeal Neoplasms / surgery

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  • (PMID = 17828107.001).
  • [ISSN] 0042-4668
  • [Journal-full-title] Vestnik otorinolaringologii
  • [ISO-abbreviation] Vestn. Otorinolaringol.
  • [Language] rus
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] Russia (Federation)
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66. 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

  • [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

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  • (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
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67. Weiss ET, Geronemus RG: New technique using combined pulsed dye laser and fractional resurfacing for treating facial angiofibromas in tuberous sclerosis. Lasers Surg Med; 2010 Jul;42(5):357-60
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] New technique using combined pulsed dye laser and fractional resurfacing for treating facial angiofibromas in tuberous sclerosis.
  • BACKGROUND AND OBJECTIVE: Tuberous sclerosis (TS) is a well-described genetic disorder that is classically associated with up to hundreds of facial angiofibromas.
  • STUDY DESIGN/PATIENTS AND METHODS: We report a combinatorial technique for treating the angiofibromas of TS.
  • RESULTS: In all presented cases, improvement in the number and appearance of facial angiofibromas and erythema is noted.
  • CONCLUSION: The technique of electrosurgery, pulsed-dye laser treatment, and AFR represents a new and safe therapeutic option for treating facial angiofibromas associated with TS.
  • [MeSH-major] Angiofibroma / etiology. Angiofibroma / surgery. Facial Neoplasms / etiology. Facial Neoplasms / surgery. Laser Therapy / methods. Lasers, Dye / therapeutic use. Skin Neoplasms / etiology. Skin Neoplasms / surgery. Tuberous Sclerosis / complications

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  • (PMID = 20583249.001).
  • [ISSN] 1096-9101
  • [Journal-full-title] Lasers in surgery and medicine
  • [ISO-abbreviation] Lasers Surg Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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68. Onerci M, Gumus K, Cil B, Eldem B: A rare complication of embolization in juvenile nasopharyngeal angiofibroma. Int J Pediatr Otorhinolaryngol; 2005 Mar;69(3):423-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A rare complication of embolization in juvenile nasopharyngeal angiofibroma.
  • Juvenile nasopharyngeal angiofibroma (JNA) is one of the most common benign nasal cavity tumors of adolescence.
  • It exhibits a strong tendency to bleed and despite being microscopically benign, its behavior is locally aggressive.
  • In this article, a young male with juvenile nasopharyngeal angiofibroma, who lost his vision in the left eye following embolization was presented and the possible therapeutic options in such a complication were discussed.
  • [MeSH-major] Angiofibroma / pathology. Angiofibroma / therapy. Embolization, Therapeutic / methods. Nasopharyngeal Neoplasms / pathology. Nasopharyngeal Neoplasms / therapy

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  • (PMID = 15733605.001).
  • [ISSN] 0165-5876
  • [Journal-full-title] International journal of pediatric otorhinolaryngology
  • [ISO-abbreviation] Int. J. Pediatr. Otorhinolaryngol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Ireland
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69. Gramann M, Wendler O, Haeberle L, Schick B: Expression of collagen types I, II and III in juvenile angiofibromas. Cells Tissues Organs; 2009;189(6):403-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Expression of collagen types I, II and III in juvenile angiofibromas.
  • Extracellular matrix components have rarely been the focus of interest in juvenile angiofibroma (JA) studies.
  • [MeSH-major] Angiofibroma / metabolism. Fibrillar Collagens / metabolism

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  • [Copyright] (c) 2008 S. Karger AG, Basel.
  • (PMID = 18815441.001).
  • [ISSN] 1422-6421
  • [Journal-full-title] Cells, tissues, organs
  • [ISO-abbreviation] Cells Tissues Organs (Print)
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Switzerland
  • [Chemical-registry-number] 0 / Fibrillar Collagens
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70. Huang XM, Sun W, Zheng YQ, Peng JR, Zeng L, Zuo H, Xu YD: [Analysis of surgical treatment of nasopharyngeal angiofibroma]. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2006 Nov;41(11):818-20

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Analysis of surgical treatment of nasopharyngeal angiofibroma].
  • OBJECTIVE: To study the individual surgical treatment of nasopharyngeal angiofibroma.
  • 2004, different kinds of surgical approaches in 51 patients with angiofibromas were retrospectively analysed.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Otorhinolaryngologic Surgical Procedures

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  • (PMID = 17283533.001).
  • [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; Journal Article
  • [Publication-country] China
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71. Klockars T, Renkonen S, Leivo I, Hagström J, Mäkitie AA: Juvenile nasopharyngeal angiofibroma: no evidence for inheritance or association with familial adenomatous polyposis. Fam Cancer; 2010 Sep;9(3):401-3
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Juvenile nasopharyngeal angiofibroma: no evidence for inheritance or association with familial adenomatous polyposis.
  • Juvenile nasopharyngeal angiofibromas (JNAs) are rare tumors with prominent vascularity and locally destructive growth.
  • Twenty-one patients diagnosed with juvenile angiofibroma filled out a detailed patient questionnaire.
  • No patients reported any relatives with nasopharyngeal angiofibroma or familial adenomatous polyposis.
  • [MeSH-major] Adenomatous Polyposis Coli / genetics. Angiofibroma / genetics. Genetic Predisposition to Disease. Nasopharyngeal Neoplasms / genetics

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  • (PMID = 20229070.001).
  • [ISSN] 1573-7292
  • [Journal-full-title] Familial cancer
  • [ISO-abbreviation] Fam. Cancer
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] Netherlands
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72. Jeyanthi K, Karthikeyan R, Sherlin HJ, Anuja N, Ramani P, Priya P, Chandrasekar T, Khan N, Narayanan V: Pleomorphic adenoma in the infra-temporal space: the first case report. Head Neck Pathol; 2007 Dec;1(2):173-7

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Tumors that are reported commonly in the infratemporal region are nasopharyngeal carcinomas, juvenile angiofibromas and adenoid cystic carcinomas.
  • To the best of our knowledge, this is the first report in the English language literature of a pleomorphic adenoma presenting in the infratemporal space and probably arising from an ectopic minor salivary gland, along with a brief description of the surgical technique.

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  • [Cites] Neurosurgery. 1999 Dec;45(6):1385-98 [10598707.001]
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  • (PMID = 20614271.001).
  • [ISSN] 1936-0568
  • [Journal-full-title] Head and neck pathology
  • [ISO-abbreviation] Head Neck Pathol
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Other-IDs] NLM/ PMC2807513
  • [Keywords] NOTNLM ; Infratemporal fossa / Pleomorphic adenoma
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73. Oueslati S, Gamra OB, Kharrat S, Sassi S, Milka N, Rajhi H, Mbarek CH, Sahtout S, Menif E, Mnif N: [Nasopharyngeal angiofibroma: report of 15 cases treated by embolization]. J Radiol; 2008 May;89(5 Pt 1):579-84

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Nasopharyngeal angiofibroma: report of 15 cases treated by embolization].
  • [Transliterated title] Le fibrome nasopharyngien: à propos de 15 cas traités par embolisation.
  • PURPOSE: To report a series of 15 new cases of nasopharyngeal angiofibroma treated with presurgical embolization along with a review of the literature.
  • MATERIALS AND METHOD: Retrospective review of 15 cases of nasopharyngeal angiofibroma treated with presurgical embolization.
  • Two cases of recurrent disease and 1 case of residual tumor were noted and treated by repeat embolization.
  • [MeSH-major] Angiofibroma / therapy. Embolization, Therapeutic / methods. Nasopharyngeal Neoplasms / therapy

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  • (PMID = 18535499.001).
  • [ISSN] 0221-0363
  • [Journal-full-title] Journal de radiologie
  • [ISO-abbreviation] J Radiol
  • [Language] fre
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] France
  • [Chemical-registry-number] 0 / Polyvinyls; 0 / ivalon sponge
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74. 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
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  • [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

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  • (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
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75. 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
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  • [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

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  • (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
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76. Chen MK, Tsai YL, Lee KW, Chang CC: Strictly endoscopic and harmonic scalpel-assisted surgery of nasopharyngeal angiofibromas: eligible for advanced stage tumors. Acta Otolaryngol; 2006 Dec;126(12):1321-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Strictly endoscopic and harmonic scalpel-assisted surgery of nasopharyngeal angiofibromas: eligible for advanced stage tumors.
  • CONCLUSIONS: With the assistance of the harmonic scalpel, endoscopic surgery is eligible for advanced nasopharyngeal angiofibromas with skull base or infratemoporal fossa invasion.
  • OBJECTIVES: To evaluate the safety and efficacy of strictly endoscopic removal of early and advanced stage nasopharyngeal angiofibromas.
  • Eight operations for seven consecutive patients presenting with a nasopharyngeal angiofibroma were performed via minimally invasive endoscopic resection by a single surgeon (M.K.C.).
  • [MeSH-major] Angiofibroma / surgery. Endoscopy. Nasopharyngeal Neoplasms / surgery. Ultrasonic Therapy / instrumentation

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  • (PMID = 17101595.001).
  • [ISSN] 0001-6489
  • [Journal-full-title] Acta oto-laryngologica
  • [ISO-abbreviation] Acta Otolaryngol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Norway
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77. Zhang XM, Teng YS, Wen WP, Cai Q, Wang DL: [Endoscopic surgery for nasopharyngeal angiofibroma]. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2006 Aug;41(8):579-82
MedlinePlus Health Information. consumer health - Endoscopy.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Endoscopic surgery for nasopharyngeal angiofibroma].
  • OBJECTIVE: To investigate the efficacy and the surgical techniques of transnasal endoscopic procedure for juvenile nasopharyngeal angiofibroma (JNA).
  • METHODS: Twenty-one nasopharyngeal angiofibroma patients were treated using transnasal endoscopic approach.
  • [MeSH-major] Angiofibroma / surgery. Endoscopy / methods. Nasopharyngeal Neoplasms / surgery

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  • (PMID = 17039797.001).
  • [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
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78. Robson CD: Imaging of head and neck neoplasms in children. Pediatr Radiol; 2010 Apr;40(4):499-509
MedlinePlus Health Information. consumer health - Head and Neck Cancer.

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • 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.

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  • (PMID = 20225112.001).
  • [ISSN] 1432-1998
  • [Journal-full-title] Pediatric radiology
  • [ISO-abbreviation] Pediatr Radiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Germany
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79. Unsal Tuna E, Karaca C, Kaymakçi M, Ozbek C, Ozdem C: [Transpalatal approach in juvenile nasopharyngeal angiofibroma]. Kulak Burun Bogaz Ihtis Derg; 2007;17(1):7-12

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] [Transpalatal approach in juvenile nasopharyngeal angiofibroma].
  • [Transliterated title] Juvenil nazofarenks anjiyofibromunda transpalatal yaklaşim.
  • OBJECTIVES: Juvenile nasopharyngeal angiofibroma (JNA) cases treated with transpalatal approach were evaluated with respect to localization, complications, intraoperative blood loss, recurrence, and prognosis.
  • RESULTS: Three patients (20%) had Chandler stage II, 11 patients (73%) had stage III, and one patient (7%) had stage IV disease.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Neoplasm Recurrence, Local / surgery. Palate / surgery

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  • (PMID = 17483604.001).
  • [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; Evaluation Studies; Journal Article
  • [Publication-country] Turkey
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80. Gaillard AL, Anastácio VM, Piatto VB, Maniglia JV, Molina FD: A seven-year experience with patients with juvenile nasopharyngeal angiofibroma. Braz J Otorhinolaryngol; 2010 Mar-Apr;76(2):245-50

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A seven-year experience with patients with juvenile nasopharyngeal angiofibroma.
  • Juvenile nasopharyngeal angiofibroma (JNA) is a rare tumor in adolescent males.
  • [MeSH-major] Angiofibroma / therapy. Embolization, Therapeutic. Nasopharyngeal Neoplasms / therapy

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  • (PMID = 20549087.001).
  • [ISSN] 1808-8686
  • [Journal-full-title] Brazilian journal of otorhinolaryngology
  • [ISO-abbreviation] Braz J Otorhinolaryngol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Brazil
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81. Chiang YY, Tsai HH, Lee WR, Wang KH: Clear cell fibrous papule: report of a case mimicking a balloon cell nevus. J Cutan Pathol; 2009 Mar;36(3):381-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Clear cell fibrous papule: report of a case mimicking a balloon cell nevus.
  • Clear cell fibrous papule (FP) is a rare variant of FP.
  • We report a 39-year-old female patient who presented with a dome-shaped papule on the nose.
  • Interestingly, scattered S-100 cells were admixed within the lesion, a finding hitherto not reported.

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  • (PMID = 19220636.001).
  • [ISSN] 1600-0560
  • [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 / Neoplasm Proteins; 0 / S100 Proteins
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82. Kania RE, Sauvaget E, Guichard JP, Chapot R, Huy PT, Herman P: Early postoperative CT scanning for juvenile nasopharyngeal angiofibroma: detection of residual disease. AJNR Am J Neuroradiol; 2005 Jan;26(1):82-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Early postoperative CT scanning for juvenile nasopharyngeal angiofibroma: detection of residual disease.
  • BACKGROUND AND PURPOSE: High recurrence rates and early recurrence have been reported for juvenile nasopharyngeal angiofibroma (JNA) involving the skull base.
  • The purpose of this study was to evaluate the diagnostic accuracy of contrast-enhanced CT scanning for the detection of residual disease (RD) in the early postoperative course after surgical excision of JNA.
  • Variabilities in readers' interpretations were encountered for false-positive results and for disease in the foramen lacerum.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Neoplasm, Residual / radiography. Postoperative Complications / radiography. Tomography, X-Ray Computed

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  • (PMID = 15661706.001).
  • [ISSN] 0195-6108
  • [Journal-full-title] AJNR. American journal of neuroradiology
  • [ISO-abbreviation] AJNR Am J Neuroradiol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, Helminth; 0 / DiAg protein, Dirofilaria immitis
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83. Ereño C, López JI, Pérez J, Grande J, Bilbao FJ: Orbital giant cell angiofibroma. APMIS; 2006 Sep;114(9):663-5

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Orbital giant cell angiofibroma.
  • A case of giant cell angiofibroma in a 73-year-old man is reported.
  • The clinicopathological features of this rare neoplasm--that is nowadays considered a variant of solitary fibrous tumour--are reviewed and briefly commented on.
  • [MeSH-major] Angiofibroma / diagnosis. Angiofibroma / pathology. Neoplasm Recurrence, Local / diagnosis. Neoplasms, Fibrous Tissue / diagnosis. Orbital Neoplasms / diagnosis

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  • (PMID = 16948822.001).
  • [ISSN] 0903-4641
  • [Journal-full-title] APMIS : acta pathologica, microbiologica, et immunologica Scandinavica
  • [ISO-abbreviation] APMIS
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Denmark
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84. González-Pérez LM, Sánchez-Gallego F, Haro-Luna JJ, Infante-Cossío P: Giant cell angiofibroma of parapharyngeal space: a report of a new location for a rare tumour. Int J Oral Maxillofac Surg; 2010 Oct;39(10):1024-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Giant cell angiofibroma of parapharyngeal space: a report of a new location for a rare tumour.
  • Giant cell angiofibroma was first described as a distinctive orbital soft-tissue tumour in male adults; it is now recognized that this mesenchymal tumour can present in other anatomical regions.
  • In this article, a case of giant cell angiofibroma of parapharyngeal space in a 25-year-old woman is described.
  • To the authors' knowledge, this is the first reported case of giant cell angiofibroma arising in the parapharyngeal space.
  • [MeSH-major] Angiofibroma / diagnosis. Parotid Neoplasms / diagnosis. Pharyngeal Neoplasms / diagnosis

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  • [Copyright] Copyright © 2010 International Association of Oral and Maxillofacial Surgeons. Published by Elsevier Ltd. All rights reserved.
  • (PMID = 20537864.001).
  • [ISSN] 1399-0020
  • [Journal-full-title] International journal of oral and maxillofacial surgery
  • [ISO-abbreviation] Int J Oral Maxillofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Denmark
  • [Chemical-registry-number] 0 / Antigens, CD; 0 / Antigens, CD34; 0 / CD99 protein, human; 0 / Cell Adhesion Molecules; 0 / Proto-Oncogene Proteins c-bcl-2; 0 / Vimentin
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85. 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
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  • [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

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  • (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
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86. 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

  • [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.

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  • [Cites] J Clin Pathol. 2007 Jul;60(7):798-803 [16816171.001]
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  • [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
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87. Ashraf M, Kumar P, Reza MA, Ragesh KP: Neoplastic diseases of the head & neck in children. Indian J Otolaryngol Head Neck Surg; 2006 Oct;58(4):343-6

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Neoplastic diseases of the head & neck in children.
  • The cervicofacial malignancies presents a unique challenge owing to potential adverse effects of both the disease process and the treatment employed on critical developing head and neck structures.This study comprised of 106 children below 12 years age group conducted during 1999-2003 at JNMC, Aligarh.
  • Of 106 cases 70 were benign neoplasms and 36 malignant neoplasms.
  • Nasopharyngeal angiofibroma was the commonest benign tumour and lymphoma was the commonest malignant neoplasm.
  • Team approach is required for mitigation of the disease process.

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  • (PMID = 23120341.001).
  • [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/ PMC3450388
  • [Keywords] NOTNLM ; Lymphoma / Nasopharyngeal angiofibroma / Neoplasm / Rhabdomyosarcoma
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88. Grieb S, Kruse R, Bruch-Gerharz D, Reifenberger J: [Tuberous sclerosis: diagnostic criteria and new treatment approaches]. Hautarzt; 2008 Oct;59(10):774-6
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Treatment for many years consisted solely in using nonspecific symptomatic approaches; dermatological therapy comprised mainly laser or electroacoustic ablation of facial angiofibromas.
  • [MeSH-major] Dermatologic Agents / therapeutic use. Interferon-gamma / therapeutic use. Skin Diseases / diagnosis. Skin Diseases / drug therapy. Tuberous Sclerosis / diagnosis. Tuberous Sclerosis / drug therapy

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  • (PMID = 18806968.001).
  • [ISSN] 1432-1173
  • [Journal-full-title] Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete
  • [ISO-abbreviation] Hautarzt
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
  • [Chemical-registry-number] 0 / Dermatologic Agents; 0 / Recombinant Proteins; 82115-62-6 / Interferon-gamma
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89. Liao H, Hua QQ, Wu ZY: [Maxillary swing approach in the management of tumors in the central and lateral cranial base]. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2006 Apr;41(4):276-80

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Among them, five suffered from chordoma, two had rhabdomyosarcoma, two had squamous cell carcinoma, one had malignant fibrous histiocytoma, one had malignant melanoma, one had esthesioneuroblastoma, one had invaded hypophysoma, two had schwannoma, one had pleomorphic adenoma, and one had angiofibroma.

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  • (PMID = 16848177.001).
  • [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
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90. Solomon D, Isaacson G: Transoral "adenoidectomy" excision of juvenile nasopharyngeal angiofibromas. Ann Otol Rhinol Laryngol; 2007 Apr;116(4):243-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Transoral "adenoidectomy" excision of juvenile nasopharyngeal angiofibromas.
  • OBJECTIVES: We describe a minimally invasive technique for excision of selected juvenile nasopharyngeal angiofibromas (JNAs) using indirect visualization of the nasopharynx.
  • The subjects included 4 teenage boys with early-stage nasopharyngeal angiofibromas.
  • All 4 boys are free of disease.
  • [MeSH-major] Adenoidectomy / methods. Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery
  • [MeSH-minor] Adolescent. Angiography. Disease-Free Survival. Follow-Up Studies. Humans. Magnetic Resonance Imaging. Male. Mouth. Neoplasm Staging. Retrospective Studies. Time Factors. Tomography, X-Ray Computed. Treatment Outcome

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  • (PMID = 17491520.001).
  • [ISSN] 0003-4894
  • [Journal-full-title] The Annals of otology, rhinology, and laryngology
  • [ISO-abbreviation] Ann. Otol. Rhinol. Laryngol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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91. Hackman T, Snyderman CH, Carrau R, Vescan A, Kassam A: Juvenile nasopharyngeal angiofibroma: The expanded endonasal approach. Am J Rhinol Allergy; 2009 Jan-Feb;23(1):95-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Juvenile nasopharyngeal angiofibroma: The expanded endonasal approach.
  • BACKGROUND: Juvenile nasopharyngeal angiofibroma (JNA) is a benign but locally aggressively vascular tumor that may involve the skull base and extend intracranially.
  • [MeSH-major] Angiofibroma / surgery. Endoscopy / methods. Nasopharyngeal Neoplasms / surgery. Otorhinolaryngologic Surgical Procedures / methods

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  • (PMID = 19379621.001).
  • [ISSN] 1945-8924
  • [Journal-full-title] American journal of rhinology & allergy
  • [ISO-abbreviation] Am J Rhinol Allergy
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] United States
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92. McAfee WJ, Morris CG, Amdur RJ, Werning JW, Mendenhall WM: Definitive radiotherapy for juvenile nasopharyngeal angiofibroma. Am J Clin Oncol; 2006 Apr;29(2):168-70
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Definitive radiotherapy for juvenile nasopharyngeal angiofibroma.
  • OBJECTIVES: To update our experience with definitive radiotherapy (RT) for juvenile nasopharyngeal angiofibroma (JNA).
  • [MeSH-major] Angiofibroma / radiotherapy. Nasopharyngeal Neoplasms / radiotherapy

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  • (PMID = 16601437.001).
  • [ISSN] 1537-453X
  • [Journal-full-title] American journal of clinical oncology
  • [ISO-abbreviation] Am. J. Clin. Oncol.
  • [Language] eng
  • [Publication-type] Clinical Trial; Journal Article
  • [Publication-country] United States
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93. Cansiz H, Güvenç MG, Sekercioğlu N: Surgical approaches to juvenile nasopharyngeal angiofibroma. J Craniomaxillofac Surg; 2006 Jan;34(1):3-8

  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Surgical approaches to juvenile nasopharyngeal angiofibroma.
  • INTRODUCTION: Juvenile nasopharyngeal angiofibromas are highly vascular, non-encapsulated tumours affecting predominantly young males.
  • These lesions are benign histologically but they may become life-threatening with excessive bleeding or intracranial extension.
  • MATERIAL AND METHODS: The surgical approaches to 22 male patients with nasopharyngeal angiofibromas are reviewed.
  • CONCLUSION: The suggested treatment of juvenile nasopharyngeal angiofibroma consists of an endoscopic transnasal approach for early stage lesions, and a modified midfacial degloving for almost all of the advanced lesions.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Oral Surgical Procedures / methods
  • [MeSH-minor] Adolescent. Adult. Carotid Artery Injuries / etiology. Carotid Artery, Internal / pathology. Child. Craniotomy / adverse effects. Endoscopy. Facial Paralysis / etiology. Frontal Bone / surgery. Humans. Male. Neoplasm Staging. Nose / surgery. Nose Diseases / etiology. Paresthesia / etiology. Postoperative Complications. Retrospective Studies. Rupture. Temporal Bone / surgery. Treatment Outcome

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  • (PMID = 16343920.001).
  • [ISSN] 1010-5182
  • [Journal-full-title] Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery
  • [ISO-abbreviation] J Craniomaxillofac Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Scotland
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94. Janaki MG, Nirmala S, Rajeev AG: Nasopharyngeal angiofibroma treated with radiotherapy. J Cancer Res Ther; 2007 Apr-Jun;3(2):100-1

  • [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

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  • (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
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95. Zoumalan CI, Egbert PR, Warwar RE, McCulley TJ: Orbital giant cell angiofibroma recurring as a solitary fibrous tumor. Ophthal Plast Reconstr Surg; 2008 Jul-Aug;24(4):325-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Orbital giant cell angiofibroma recurring as a solitary fibrous tumor.
  • Giant cell angiofibroma has recently been hypothesized to be a clinicopathologic variant of solitary fibrous tumor.
  • The authors report a case of an orbital giant cell angiofibroma that recurred as a solitary fibrous tumor 4 years later.
  • The report strongly supports the hypothesis that giant cell angiofibroma and solitary fibrous tumor are related.
  • [MeSH-major] Angiofibroma / pathology. Giant Cells / pathology. Neoplasm Recurrence, Local / pathology. Orbital Neoplasms / pathology. Solitary Fibrous Tumors / pathology

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  • (PMID = 18645449.001).
  • [ISSN] 0740-9303
  • [Journal-full-title] Ophthalmic plastic and reconstructive surgery
  • [ISO-abbreviation] Ophthal Plast Reconstr Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Neoplasm Proteins
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96. Schlauder SM, Knapp C, Steffensen TS, Bui MM: Aromatase may play a critical role in the pathogenesis of juvenile nasopharyngeal angiofibroma. Fetal Pediatr Pathol; 2009;28(5):232-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Aromatase may play a critical role in the pathogenesis of juvenile nasopharyngeal angiofibroma.
  • The pathophysiology of juvenile nasopharyngeal angiofibroma (JNA) has yet to be fully elucidated, but the influence of steroid hormones in their growth has been suggested.
  • [MeSH-major] Angiofibroma / pathology. Aromatase / metabolism. Nasopharyngeal Neoplasms / pathology

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  • (PMID = 19842877.001).
  • [ISSN] 1551-3823
  • [Journal-full-title] Fetal and pediatric pathology
  • [ISO-abbreviation] Fetal Pediatr Pathol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Androgens; 0 / Receptors, Androgen; 0 / Receptors, Estrogen; EC 1.14.14.1 / Aromatase
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97. 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
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  • [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

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  • (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
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98. 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

  • [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

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  • (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
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99. Eloy P, Watelet JB, Hatert AS, de Wispelaere J, Bertrand B: Endonasal endoscopic resection of juvenile nasopharyngeal angiofibroma. Rhinology; 2007 Mar;45(1):24-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Endonasal endoscopic resection of juvenile nasopharyngeal angiofibroma.
  • Juvenile angiofibroma (JNA) is a rare benign but locally aggressive tumour of the nasopharynx that primarily occurs in adolescent males.
  • According to Radkowski's classification (Table 1), one patient was stage Ia, one was stage Ib and four patients were stage IIb.
  • All patients but one were free of disease.
  • Based upon the recent international literature, endonasal surgery combined with a preoperative embolization of the arterial supply is indicated for small and middle size JNAs but also for large tumours extended to the pterygopalatine fossa and medial aspect of the infratemporal fossa.
  • [MeSH-major] Angiofibroma / surgery. Endoscopy / methods. Nasopharyngeal Neoplasms / surgery

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  • (PMID = 17432065.001).
  • [ISSN] 0300-0729
  • [Journal-full-title] Rhinology
  • [ISO-abbreviation] Rhinology
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Netherlands
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100. 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

  • [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

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  • (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] Italy
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Neoplasm Proteins
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