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1. Lee CH, Hong CH, Yu HS, Chen GS, Yang KC: Transforming growth factor-β enhances matrix metalloproteinase-2 expression and activity through AKT in fibroblasts derived from angiofibromas in patients with tuberous sclerosis complex. Br J Dermatol; 2010 Dec;163(6):1238-44
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Transforming growth factor-β enhances matrix metalloproteinase-2 expression and activity through AKT in fibroblasts derived from angiofibromas in patients with tuberous sclerosis complex.
  • BACKGROUND: Patients with tuberous sclerosis complex (TSC) develop fibrous tumours in the brain, skin, kidney, heart and lungs due to TSC1/2 mutations.
  • In the skin, patients develop angiofibromas that have vascular and fibrotic components in which transforming growth factor (TGF)-β and matrix metalloproteinase (MMP)-2 are important.
  • OBJECTIVES: To investigate if the TGF-β axis and MMP-2 play an important role in the pathogenesis of TSC angiofibromas.
  • METHODS: Samples from TSC angiofibromas and normal skin were measured for expression of TGF-β and MMP-2 by immunohistochemistry and real-time polymerase chain reaction.
  • Fibroblasts grown from TSC angiofibromas (TSC fibroblasts) were incubated with TGF-β.
  • [MeSH-major] Angiofibroma / enzymology. Fibroblasts / enzymology. Matrix Metalloproteinase 2 / metabolism. Transforming Growth Factor beta / pharmacology. Tuberous Sclerosis / enzymology

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  • [Copyright] © 2010 The Authors. BJD © 2010 British Association of Dermatologists.
  • (PMID = 20698845.001).
  • [ISSN] 1365-2133
  • [Journal-full-title] The British journal of dermatology
  • [ISO-abbreviation] Br. J. Dermatol.
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] England
  • [Chemical-registry-number] 0 / Transforming Growth Factor beta; EC 2.7.11.1 / Proto-Oncogene Proteins c-akt; EC 2.7.11.24 / Extracellular Signal-Regulated MAP Kinases; EC 3.4.24.24 / Matrix Metalloproteinase 2
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2. Danesi G, Panciera DT, Harvey RJ, Agostinis C: Juvenile nasopharyngeal angiofibroma: evaluation and surgical management of advanced disease. Otolaryngol Head Neck Surg; 2008 May;138(5):581-6
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  • [Title] Juvenile nasopharyngeal angiofibroma: evaluation and surgical management of advanced disease.
  • Describe the outcomes in surgically treated juvenile nasopharyngeal angiofibroma (JNA) with the influence of middle cranial fossa, carotid, or dural involvement on recurrence.
  • RESULTS: Recurrence for advanced disease (IIIb+) was 18.2% (6 of 33) and 15.3% (13 of 85) overall.
  • CONCLUSION: Dural involvement by tumor is rare and imaging may overstage disease.
  • When an open approach is used, a midface degloving technique affords excellent exposure even for advanced disease.
  • Lateral approaches with their associated morbidity can be reserved for selected recurrent disease.
  • [MeSH-major] Angiofibroma / diagnosis. Angiofibroma / surgery. Nasopharyngeal Neoplasms / diagnosis. Nasopharyngeal Neoplasms / surgery

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  • (PMID = 18439462.001).
  • [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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3. Hillel AT, Metzinger RC, Nemechek AJ, Nuss DW: Loss of reflex tearing: an expected consequence of juvenile nasopharyngeal angiofibroma. Otolaryngol Head Neck Surg; 2005 Oct;133(4):605-10
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  • [Title] Loss of reflex tearing: an expected consequence of juvenile nasopharyngeal angiofibroma.
  • OBJECTIVE: To report the loss of reflex tearing after surgical treatment of juvenile nasopharyngeal angiofibroma (JNA).
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Postoperative Complications. Reflex, Abnormal. Xerophthalmia / etiology

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  • (PMID = 16213937.001).
  • [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] Case Reports; Journal Article
  • [Publication-country] United States
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4. Herzallah IR, Elsheikh EM, Casiano RR: Endoscopic endonasal study of the maxillary nerve: a new orientation. Am J Rhinol; 2007 Sep-Oct;21(5):637-43
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-minor] Angiofibroma / diagnosis. Angiofibroma / pathology. Cadaver. Humans. Maxillary Artery / anatomy & histology. Maxillary Artery / pathology. Microscopy, Video / methods. Minimally Invasive Surgical Procedures. Models, Anatomic. Nasal Cavity. Trigeminal Nerve / anatomy & histology. Trigeminal Nerve / pathology. Video Recording

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  • (PMID = 17999805.001).
  • [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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5. 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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  • (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
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6. Sinha R, Das S, Ray S, Banerjee P, Sadhu P: Nasopharyngeal angiofibroma: rare presentations. Ear Nose Throat J; 2008 Dec;87(12):E26
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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: rare presentations.
  • Nasopharyngeal angiofibromas are benign tumors of the nasopharynx that occur in adolescent boys.
  • Two interesting cases of angiofibroma with atypical presentations, showing extensive spread in multiple directions, are reported here.
  • In one case, the angiofibroma exited the right nostril as a large polypoidal mass and also presented as an intraoral tumor in the right upper gingivo-alveolar region.
  • [MeSH-major] Angiofibroma / pathology. Nasopharyngeal Neoplasms / pathology

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  • (PMID = 19105131.001).
  • [ISSN] 1942-7522
  • [Journal-full-title] Ear, nose, & throat journal
  • [ISO-abbreviation] Ear Nose Throat J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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7. 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
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  • [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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8. Samaratunga H, Fitzpatrick P: Cellular angiofibroma of the scrotum. Pathology; 2008 Apr;40(3):330-3
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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 of the scrotum.
  • [MeSH-major] Angiofibroma / pathology. Genital Neoplasms, Male / pathology. Scrotum / pathology

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  • (PMID = 18428064.001).
  • [ISSN] 0031-3025
  • [Journal-full-title] Pathology
  • [ISO-abbreviation] Pathology
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] England
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9. Liu JT, Briner RP, Friedman JA: Comparison of inpatient vs. outpatient anterior cervical discectomy and fusion: a retrospective case series. BMC Surg; 2009;9:3
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  • METHODS: All patients undergoing single-level anterior cervical discectomy and fusion with plating between August 2005 and May 2007 by two surgeons (RPB or JAF) were retrospectively reviewed.

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  • (PMID = 19265540.001).
  • [ISSN] 1471-2482
  • [Journal-full-title] BMC surgery
  • [ISO-abbreviation] BMC Surg
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2657115
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10. Micheletti AM, Silva AC, Nascimento AG, Da Silva CS, Murta EF, Adad SJ: Cellular angiofibroma of the vulva: case report with clinicopathological and immunohistochemistry study. Sao Paulo Med J; 2005 Sep 1;123(5):250-2
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  • [Title] Cellular angiofibroma of the vulva: case report with clinicopathological and immunohistochemistry study.
  • CONTEXT: Cellular angiofibroma of the vulva is a rare tumor that was first described in 1997.
  • The differential diagnoses for this tumor include aggressive angiomyxoma, angiomyofibroblastoma, lipoma of fusiform cells, solitary fibrous tumor, perineurioma and leiomyoma.
  • [MeSH-major] Angiofibroma / diagnosis. Bartholin's Glands. Cysts / diagnosis. Vulvar Neoplasms / diagnosis

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  • (PMID = 16358102.001).
  • [ISSN] 1516-3180
  • [Journal-full-title] São Paulo medical journal = Revista paulista de medicina
  • [ISO-abbreviation] Sao Paulo Med J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Brazil
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11. Montag AG, Tretiakova M, Richardson M: Steroid hormone receptor expression in nasopharyngeal angiofibromas. Consistent expression of estrogen receptor beta. Am J Clin Pathol; 2006 Jun;125(6):832-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Steroid hormone receptor expression in nasopharyngeal angiofibromas. Consistent expression of estrogen receptor beta.
  • Nasopharyngeal angiofibroma is an uncommon tumor arising in adolescent males, suggesting that the tumor may be hormonally responsive.
  • The recently described ss receptor for estrogen has not been analyzed in angiofibroma.
  • We analyzed 13 cases of nasal angiofibroma by immunohistochemical analysis for the presence of ARs, progesterone receptors (PR), and ER-a and ER-ss.
  • The findings confirm that nasopharyngeal angiofibromas express ER and suggest that new modulators of ER-ss activity may provide an alternative therapy for these lesions.
  • [MeSH-major] Angiofibroma / metabolism. Estrogen Receptor beta / metabolism. Nasopharyngeal Neoplasms / metabolism. Receptors, Androgen / metabolism. Receptors, Progesterone / metabolism

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  • (PMID = 16690481.001).
  • [ISSN] 0002-9173
  • [Journal-full-title] American journal of clinical pathology
  • [ISO-abbreviation] Am. J. Clin. Pathol.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Estrogen Receptor beta; 0 / Receptors, Androgen; 0 / Receptors, Progesterone
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12. Eloy P, Bachy V, Grulois V, Bertrand B: Pyocele of the lachrymal sac: A late and unusual complication after surgery for a juvenile nasopharyngeal angiofibroma. Clin Ophthalmol; 2008 Mar;2(1):211-5
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  • [Title] Pyocele of the lachrymal sac: A late and unusual complication after surgery for a juvenile nasopharyngeal angiofibroma.
  • JNA (Juvenile nasopharyngeal angiofibroma) is a benign but highly vascular and aggressive tumor that takes its origin in the basisphenoid region close to the sphenopalatine foramen.
  • The authors report a case of a pyocele of the lachrymal sac occurring 60 years after a transantral surgery for a JNA.
  • This case confirms the necessity of a long follow-up for all the patients who had a transantral surgery with resection of the medial wall of the maxillary sinus and dissection of the nasolacrymal duct.

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  • (PMID = 19668408.001).
  • [ISSN] 1177-5467
  • [Journal-full-title] Clinical ophthalmology (Auckland, N.Z.)
  • [ISO-abbreviation] Clin Ophthalmol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] New Zealand
  • [Other-IDs] NLM/ PMC2698692
  • [Keywords] NOTNLM ; JNA / complication / endonasal DCR / navigation system / pyocele of the lachrymal sac / surgery for JNA
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13. Demirci H, Shields CL, Eagle RC Jr, Shields JA: Giant cell angiofibroma, a variant of solitary fibrous tumor, of the orbit in a 16-year-old girl. Ophthal Plast Reconstr Surg; 2009 Sep-Oct;25(5):402-4
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  • [Title] Giant cell angiofibroma, a variant of solitary fibrous tumor, of the orbit in a 16-year-old girl.
  • Five years later, her symptoms recurred, and she was referred to the Oncology Service, Wills Eye Institute.
  • Histopathologic examination showed benign, patternless spindle-cell proliferation with prominent intrinsic vascularity and multinucleated giant cells, consistent with giant cell angiofibroma, a variant of solitary fibrous tumor.
  • Giant cell angiofibroma, a variant of solitary fibrous tumor, is a rare orbital tumor that presents as a well-circumscribed, enhancing mass and can be found in children.
  • [MeSH-major] Angiofibroma / pathology. Giant Cell Tumors / pathology. Orbital Neoplasms / pathology. Solitary Fibrous Tumors / pathology

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  • (PMID = 19966660.001).
  • [ISSN] 1537-2677
  • [Journal-full-title] Ophthalmic plastic and reconstructive surgery
  • [ISO-abbreviation] Ophthal Plast Reconstr Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Antigens, CD34; 0 / Biomarkers, Tumor
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14. Koop K, Van Dijk M, Van Huisseling H: A labial lump. Routine activities were impeded by an extraordinary tumor. Am J Obstet Gynecol; 2009 Dec;201(6):628.e1
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Angiofibroma / pathology. Vulvar Neoplasms / pathology

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  • (PMID = 19664749.001).
  • [ISSN] 1097-6868
  • [Journal-full-title] American journal of obstetrics and gynecology
  • [ISO-abbreviation] Am. J. Obstet. Gynecol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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15. Dubey SP, Molumi CP: Critical look at the surgical approaches of nasopharyngeal angiofibroma excision and "total maxillary swing" as a possible alternative. Ann Otol Rhinol Laryngol; 2007 Oct;116(10):723-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Critical look at the surgical approaches of nasopharyngeal angiofibroma excision and "total maxillary swing" as a possible alternative.
  • OBJECTIVES: We critically analyzed different surgical approaches used for the excision of nasopharyngeal angiofibroma (NPA) at our hospital in a 10-year period and proposed "total maxillary swing" as a possible alternative approach.
  • [MeSH-major] Angiofibroma / surgery. Maxilla / surgery. Nasopharyngeal Neoplasms / surgery. Otorhinolaryngologic Surgical Procedures / methods

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  • (PMID = 17987777.001).
  • [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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16. Jung D, Cunnane ME, Cunningham MJ: Radiology quiz case 2. Juvenile nasopharyngeal angiofibroma (JNA), Radkowski grade Ib. Arch Otolaryngol Head Neck Surg; 2010 Jul;136(7):741-3
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  • [Title] Radiology quiz case 2. Juvenile nasopharyngeal angiofibroma (JNA), Radkowski grade Ib.
  • [MeSH-major] Angiofibroma / diagnosis. Magnetic Resonance Imaging / methods. Nasopharyngeal Neoplasms / diagnosis. Radiographic Image Enhancement. Tomography, X-Ray Computed / methods

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  • (PMID = 20644076.001).
  • [ISSN] 1538-361X
  • [Journal-full-title] Archives of otolaryngology--head & neck surgery
  • [ISO-abbreviation] Arch. Otolaryngol. Head Neck Surg.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] AU0V1LM3JT / Gadolinium
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17. 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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  • [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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18. 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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  • [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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19. 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
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  • [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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21. Belmar P, Boixeda P, Baniandrés O, Fernández-Lorente M, Arrazola JM: [Long-term follow up of angiofibromas treated with CO2 laser in 23 patients with tuberous sclerosis]. Actas Dermosifiliogr; 2005 Oct;96(8):498-503
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  • [Title] [Long-term follow up of angiofibromas treated with CO2 laser in 23 patients with tuberous sclerosis].
  • [Transliterated title] Seguimiento a largo plazo de angiofibromas tratados con láser de CO2 en 23 pacientes con esclerosis tuberosa.
  • INTRODUCTION: Tuberous sclerosis is an autosomal dominant disease in which hamartomas form in multiple organs.
  • Cutaneous changes are one of the primary characteristics of this disease.
  • These include angiofibromas (AF), a common form of presentation that causes significant cosmetic and medical problems.
  • The aim of our study is to assess the long-term response of the treatment of angiofibromas.
  • METHODS: A retrospective study was carried out on 23 patients with angiofibromas treated with CO2 laser.
  • We classified the angiofibromas by size, initial treatment results and patients' ages (< 20 years and 20 years or older).
  • After treatment, patients were followed up for a period of six months to 10 years.
  • When we analyzed the long-term results by the size of the angiofibromas, initial result and patients' ages, we found no statistically significant differences among the different groups.
  • [MeSH-major] Angiofibroma / complications. Angiofibroma / surgery. Laser Therapy. Skin Neoplasms / complications. Skin Neoplasms / surgery. Tuberous Sclerosis / complications


22. Sołtys J, Pietniczka-Załeska M, Młyńczyk-Budzynowska K, Majkowski J: [Neoplasms of paranasal sinuses in material of ENT Department MSS Hospital in Warsaw between 2006-2007]. Otolaryngol Pol; 2008;62(4):451-4
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  • Tumors of paranasal sinuses present a small percent of tumors detected in the region of head and neck 3-4% and they present a fraction of a percent of tumors in general /0.16%/.
  • THE RESULTS: We detected the following:--benign neoplasms: 2 cases of angiofibroma, 3 cases of inverted papilloma;--malignant tumors: 4 cases of Ca planoepitheliale, 1 instance of adenocarcinoma, 1 instance of Ca anaplasticum, 1--melanoma, 1--esthesioneuroblastoma, 1--lymphoma malignum, 1--metastatic tumor.

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  • (PMID = 18837222.001).
  • [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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23. Vasudevan B, Sawhney MP, Radhakrishnan S, Shilpa G: Tuberous sclerosis with portal vein thrombosis, protein C and S deficiency. Indian J Dermatol Venereol Leprol; 2007 Nov-Dec;73(6):412-4
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  • On examination, angiofibromas on face, shagreen patch and periungual fibromas were observed.
  • [MeSH-minor] Adult. Angiofibroma / complications. Brain Diseases / complications. Dental Fissures / complications. Facial Neoplasms / complications. Female. Fibroma / complications. Hamartoma / complications. Humans. Kidney Diseases / complications. Retinal Diseases / complications


24. 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
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  • 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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25. Park HS, Cho S, Kim KH, Won CH: Fibrous papule of the face, clear cell type: a case report. J Eur Acad Dermatol Venereol; 2007 Oct;21(9):1267-8
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  • [Title] Fibrous papule of the face, clear cell type: a case report.
  • [MeSH-major] Fibroma / pathology. Nose Neoplasms / pathology

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  • (PMID = 17894726.001).
  • [ISSN] 0926-9959
  • [Journal-full-title] Journal of the European Academy of Dermatology and Venereology : JEADV
  • [ISO-abbreviation] J Eur Acad Dermatol Venereol
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Netherlands
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26. 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
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  • [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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27. McQueeney RJ, Ma J, Chang S, Yan JQ, Hehlen M, Trouw F: Stabilization of charge ordering in La1/3Sr2/3FeO3-delta by magnetic exchange. Phys Rev Lett; 2007 Mar 23;98(12):126402
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  • In LSFO, the measured ratio of ferromagnetic exchange between Fe3+-Fe5+ pairs (JF) and antiferromagnetic exchange between Fe3+-Fe3+ pairs (JAF) fulfills the criterion for charge ordering driven by magnetic interactions (|JF/JAF|>1).
  • The 30% reduction of JAF as compared to LFO indicates that doped holes are delocalized, and charge ordering occurs without a dominant influence from Coulomb interactions.

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  • (PMID = 17501139.001).
  • [ISSN] 0031-9007
  • [Journal-full-title] Physical review letters
  • [ISO-abbreviation] Phys. Rev. Lett.
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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28. Voykov B, Guenova E, Süsskind D, Schiefer U: [Tuberous sclerosis: an interdisciplinary diagnosis]. Klin Monbl Augenheilkd; 2007 May;224(5):441-4
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  • BACKGROUND: Tuberous sclerosis is a relatively rare disease, but it often takes a progressive and severe course.
  • FINDINGS: Ophthalmologic evaluation including funduscopy, 30 degree perimetry and fundus photography and clinical course of a 40-year-old man are described.
  • CONCLUSIONS: An ophthalmologist should always think of a tuberous sclerosis as a differential diagnosis when confronted with a retinal hamartoma.
  • Other characteristic ophthalmological findings include facial and eyelid angiofibromas, coloboma of the iris, lens and choroid, strabismus, poliosis of the eyelashes, papilloedema and sector iris depigmentation.
  • [MeSH-major] Hamartoma Syndrome, Multiple / diagnosis. Patient Care Team. Retinal Diseases / diagnosis. Tuberous Sclerosis / diagnosis


29. Choi H, Kim S, Moon JH, Lee YH, Rhee Y, Kang ES, Ahn CW, Cha BS, Lee EJ, Kim KR, Lee HC, Jeong SY, Kim HJ, Lim SK: Multiple endocrine neoplasia type 1 with multiple leiomyomas linked to a novel mutation in the MEN1 gene. Yonsei Med J; 2008 Aug 30;49(4):655-61
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  • MEN1 is characterized by the presence of functioning and nonfunctioning tumors or hyperplasia of the pituitary gland, parathyroid glands, and pancreatic islet cells.
  • In addition, MEN1 carriers can have adrenal or thyroid tumors and non-endocrine tumors, such as lipomas, angiofibromas, and leiomyomas.
  • However, there has been no report of a case of MEN1 with leiomyoma in Korea so far.


30. Poetker DM, Toohill RJ, Loehrl TA, Smith TL: Endoscopic management of sinonasal tumors: a preliminary report. Am J Rhinol; 2005 May-Jun;19(3):307-15
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  • BACKGROUND: The increased experience with the endoscopic approach to sinonasal inflammatory disease has resulted in the increased use of endoscopes to manage many different sinonasal pathologies.
  • For benign tumors, 24 patients were identified with a mean age of 50.7 years, a mean follow-up of 17.5 months, and a recurrence rate of 4.2%.
  • [MeSH-minor] Adenocarcinoma / surgery. Adenoma / surgery. Adult. Aged. Aged, 80 and over. Angiofibroma / surgery. Carcinoma, Adenoid Cystic / surgery. Carcinoma, Squamous Cell / mortality. Carcinoma, Squamous Cell / surgery. Chondrosarcoma / surgery. Esthesioneuroblastoma, Olfactory / surgery. Female. Follow-Up Studies. Hemangiopericytoma / surgery. Humans. Male. Melanoma / surgery. Middle Aged. Nasal Cavity / surgery. Neoplasm Recurrence, Local / epidemiology. Neoplasm Recurrence, Local / therapy. Osteoma / surgery. Papilloma, Inverted / surgery. Retrospective Studies. Survival Rate. Treatment Outcome

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  • (PMID = 16011140.001).
  • [ISSN] 1050-6586
  • [Journal-full-title] American journal of rhinology
  • [ISO-abbreviation] Am J Rhinol
  • [Language] eng
  • [Publication-type] Evaluation Studies; Journal Article
  • [Publication-country] United States
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31. 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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32. Parray FQ, Malik AA, Chowdri NA, Samoon H, Bakshi IA, Wani RA: Atypical presentation of a kidney tumor. J Gastrointestin Liver Dis; 2009 Mar;18(1):122-3
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  • [Title] Atypical presentation of a kidney tumor.
  • [MeSH-major] Angiofibroma / diagnosis. Kidney Neoplasms / diagnosis

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  • (PMID = 19337652.001).
  • [ISSN] 1841-8724
  • [Journal-full-title] Journal of gastrointestinal and liver diseases : JGLD
  • [ISO-abbreviation] J Gastrointestin Liver Dis
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] Romania
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33. Benatiya AI, Bouayed MA, Touiza E, Daoudi K, Mernissi FZ, Tahri H: [Bourneville's tuberous sclerosis. A case report]. J Fr Ophtalmol; 2005 Dec;28(10):e11
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  • [Transliterated title] La sclérose tubéreuse de Bourneville. A propos d'un cas.
  • INTRODUCTION: Bourneville's tuberous sclerosis (BTS) is an autosomal dominant phakomatosis characterized by the development of a benign hamartoma-like tumor, which is usually located in the skin, kidney, heart, brain, and eyes.
  • We present here a case of a retinal BTS of late diagnosis.
  • Dermatologic examination also showed facial angiofibromas.
  • The chest X-ray, renal scan, heart scan and a CT scan of the brain failed to show any other localizations of the disease.

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  • (PMID = 16395191.001).
  • [ISSN] 1773-0597
  • [Journal-full-title] Journal français d'ophtalmologie
  • [ISO-abbreviation] J Fr Ophtalmol
  • [Language] fre
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] France
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34. Feiz-Erfan I, Han PP, Spetzler RF, Porter RW, Klopfenstein JD, Ferreira MA, Beals SP, Joganic EF: Exposure of midline cranial base without a facial incision through a combined craniofacial-transfacial procedure. Neurosurgery; 2005 Jan;56(1 Suppl):28-35; discussion 28-35
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  • METHODS: Between 1992 and 1998, eight patients underwent surgery for five different anterior cranial base pathological findings: four angiofibromas, one mesenchymal chondrosarcoma, one esthesioneuroblastoma, one odontogenic myxoma, and one encephalocele.
  • In all cases, the surgical exposure consisted of a bicoronal scalp incision with a bifrontal craniotomy and fronto-orbitonasal osteotomy, and then a sublabial incision for transmaxillary exposure.

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  • (PMID = 15799790.001).
  • [ISSN] 1524-4040
  • [Journal-full-title] Neurosurgery
  • [ISO-abbreviation] Neurosurgery
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] United States
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35. Bylaite M, Ruzicka T: Images in clinical medicine. Pearly penile papules. N Engl J Med; 2007 Aug 16;357(7):691
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  • [MeSH-major] Angiofibroma / pathology. Penile Neoplasms / pathology

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  • (PMID = 17699819.001).
  • [ISSN] 1533-4406
  • [Journal-full-title] The New England journal of medicine
  • [ISO-abbreviation] N. Engl. J. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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36. 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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37. Renukananda GS, Basavaraja PK, Naik AS, Maheshwari M, Balaji NK, Thangavelu G: Atypical angiofibroma of larynx - a case report. Indian J Otolaryngol Head Neck Surg; 2008 Mar;60(1):51-2
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  • [Title] Atypical angiofibroma of larynx - a case report.
  • Primary extra nasopharyngeal angiofibroma of larynx is a very rare tumour.
  • We here by present a case of angiofibroma of larynx affecting the anterior commissure & subglottic region in larynx-a rare site of involvement.

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  • [Cites] Am J Otolaryngol. 2003 Nov-Dec;24(6):413-6 [14608576.001]
  • [Cites] J Chin Med Assoc. 2004 Jul;67(7):373-5 [15510937.001]
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  • (PMID = 23120500.001).
  • [ISSN] 2231-3796
  • [Journal-full-title] Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India
  • [ISO-abbreviation] Indian J Otolaryngol Head Neck Surg
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] India
  • [Other-IDs] NLM/ PMC3450725
  • [Keywords] NOTNLM ; Atypical angiofibroma / Extranasopharyngeal angiofibroma / Histolo gy
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38. Lin Y, Qiu JH, Qiao L, He LS, Zha DJ: Le Fort I osteotomy for extensive juvenile nasopharyngeal angiofibroma: a retrospective study. Adv Ther; 2008 Oct;25(10):1057-64
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  • [Title] Le Fort I osteotomy for extensive juvenile nasopharyngeal angiofibroma: a retrospective study.
  • INTRODUCTION: Juvenile nasopharyngeal angiofibroma (JNA) is a rare, nonencapsulated, benign neoplasm typically diagnosed in adolescent boys.
  • All the angiofibromas had extended into the pterygomaxillary space and infratemporal fossa.
  • [MeSH-major] Angiofibroma / surgery. Nasopharyngeal Neoplasms / surgery. Osteotomy, Le Fort / methods

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  • (PMID = 18836867.001).
  • [ISSN] 0741-238X
  • [Journal-full-title] Advances in therapy
  • [ISO-abbreviation] Adv Ther
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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39. Gupta SC, Sachin J, Savyasachi S, Ritesh J, Neha G, Singh HP: Solitary nasal schwannoma clinically presenting as an angiofibroma of the nasopharynx. Ear Nose Throat J; 2010 Jul;89(7):E28-30
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] Solitary nasal schwannoma clinically presenting as an angiofibroma of the nasopharynx.
  • Benign schwannomas of the nasal cavity are rare.
  • We report the case of a 17-year-old boy who presented with epistaxis associated with a unilateral nasal mass that extended into the nasopharynx.
  • In most such cases, a clinical diagnosis of angiofibroma is made.
  • [MeSH-major] Angiofibroma / diagnosis. Nasal Septum / pathology. Nasopharyngeal Neoplasms / diagnosis. Neurilemmoma / pathology. Nose Neoplasms / pathology

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  • (PMID = 20628976.001).
  • [ISSN] 1942-7522
  • [Journal-full-title] Ear, nose, & throat journal
  • [ISO-abbreviation] Ear Nose Throat J
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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40. Gore P, Theodore N, Brasiliense L, Kim LJ, Garrett M, Nakaji P, Gonzalez LF, McDougall CG, Albuquerque FC: The utility of onyx for preoperative embolization of cranial and spinal tumors. Neurosurgery; 2008 Jun;62(6):1204-11; discussion 1211-2
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  • Tumors included three juvenile nasal angiofibromas, two meningiomas, two hemangioblastomas, two metastases (renal cell and thyroid), and one giant cell tumor.

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  • (PMID = 18824987.001).
  • [ISSN] 1524-4040
  • [Journal-full-title] Neurosurgery
  • [ISO-abbreviation] Neurosurgery
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Onyx copolymer; 0 / Polyvinyls; YOW8V9698H / Dimethyl Sulfoxide
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41. Ponti G, Losi L, Pellacani G, Rossi GB, Presutti L, Mattioli F, Villari D, Wannesson L, Alicandri Ciufelli M, Izzo P, De Rosa M, Marone P, Seidenari S: Wnt pathway, angiogenetic and hormonal markers in sporadic and familial adenomatous polyposis-associated juvenile nasopharyngeal angiofibromas (JNA). Appl Immunohistochem Mol Morphol; 2008 Mar;16(2):173-8
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  • [Title] Wnt pathway, angiogenetic and hormonal markers in sporadic and familial adenomatous polyposis-associated juvenile nasopharyngeal angiofibromas (JNA).
  • Juvenile nasopharyngeal angiofibroma (JNA) is a rare, invasive, and locally destructive tumor of the nasopharynx.

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  • (PMID = 18227724.001).
  • [ISSN] 1541-2016
  • [Journal-full-title] Applied immunohistochemistry & molecular morphology : AIMM
  • [ISO-abbreviation] Appl. Immunohistochem. Mol. Morphol.
  • [Language] ENG
  • [Publication-type] Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor; 0 / Cadherins; 0 / Receptors, Androgen; 0 / Wnt Proteins; 0 / beta Catenin; EC 2.7.10.1 / Receptors, Vascular Endothelial Growth Factor
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42. 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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43. 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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  • [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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44. Camprubí M, Balaguer A, Azon Masoliver A, Jiménez-Feijoo R, Escribano Subias J: Unilateral facial angiofibromas; a review of the literature. Pediatr Dermatol; 2006 May-Jun;23(3):303-5
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  • [Title] Unilateral facial angiofibromas; a review of the literature.
  • [MeSH-major] Angiofibroma / pathology. Facial Neoplasms / pathology. Skin Neoplasms / pathology

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  • (PMID = 16780491.001).
  • [ISSN] 0736-8046
  • [Journal-full-title] Pediatric dermatology
  • [ISO-abbreviation] Pediatr Dermatol
  • [Language] eng
  • [Publication-type] Case Reports; Letter; Review
  • [Publication-country] United States
  • [Number-of-references] 11
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45. Tyagi I, Syal R, Goyal A: Recurrent and residual juvenile angiofibromas. J Laryngol Otol; 2007 May;121(5):460-7
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  • [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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46. Huang J, Sacks R, Forer M: Endoscopic resection of juvenile nasopharyngeal angiofibroma. Ann Otol Rhinol Laryngol; 2009 Nov;118(11):764-8
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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 juvenile nasopharyngeal angiofibroma.
  • OBJECTIVES: A 2-surgeon technique has been proposed that allows resection of juvenile nasopharyngeal angiofibroma (JNA) with extension into the infratemporal fossa by utilizing a septal incision for passage of a retracting instrument from the opposite nostril.
  • [MeSH-major] Angiofibroma / surgery. Endoscopy / methods. Nasopharyngeal Neoplasms / surgery

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  • (PMID = 19999360.001).
  • [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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47. Dhingra K, Singhal N, Khurana N: Poorly differentiated squamous cell carcinoma coexisting with angiofibroma and spreading as intravascular emboli in its vessels. Acta Otolaryngol; 2006 Dec;126(12):1342-4
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  • [Title] Poorly differentiated squamous cell carcinoma coexisting with angiofibroma and spreading as intravascular emboli in its vessels.
  • We report a case of a 28-year-old male who presented with epistaxis and hyponasal speech.
  • A clinical and radiological diagnosis of nasopharyngeal angiofibroma was made.
  • A diagnosis of poorly differentiated carcinoma, possibly squamous, with extensive embolization in the vessels of angiofibroma was made.
  • [MeSH-major] Angiofibroma / pathology. Carcinoma, Squamous Cell / pathology. Nasopharyngeal Neoplasms / pathology. Neoplasms, Multiple Primary / pathology. Neoplastic Cells, Circulating / pathology

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  • (PMID = 17101599.001).
  • [ISSN] 0001-6489
  • [Journal-full-title] Acta oto-laryngologica
  • [ISO-abbreviation] Acta Otolaryngol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Norway
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48. McCluggage WG: Recent developments in vulvovaginal pathology. Histopathology; 2009 Jan;54(2):156-73
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  • HMGA2 is useful in the diagnosis of aggressive angiomyxoma and its distinction from mimics, in the evaluation of resection margins and in the assessment of the presence or absence of residual disease in re-excisions.
  • Aggressive angiomyxoma is almost invariably positive with oestrogen and progesterone receptors, and there have been several reports of a dramatic reduction in size following gonadotropin releasing hormone agonist therapy.
  • Recent series of the relatively newly described entities cellular angiofibroma and superficial myofibroblastoma of the lower female genital tract have expanded upon the morphological spectrum of these neoplasms.
  • Recently described mesenchymal lesions at this site include massive oedema and prepubertal vulval fibroma.
  • Gastrointestinal stromal tumours have been described as primary neoplasms in the vagina, and rectovaginal septum and extragastrointestinal stromal tumour should be added to the differential diagnosis of a vulvovaginal mesenchymal lesion.
  • There have been new developments regarding Paget's disease of the vulva with the identification of markers that are useful in diagnosis and evidence that the neoplastic cells represent a proliferation of adnexal stem cells residing in sebaceous units.
  • [MeSH-major] Vaginal Diseases / pathology. Vulvar Diseases / pathology

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  • (PMID = 18637148.001).
  • [ISSN] 1365-2559
  • [Journal-full-title] Histopathology
  • [ISO-abbreviation] Histopathology
  • [Language] eng
  • [Publication-type] Journal Article; Review
  • [Publication-country] England
  • [Number-of-references] 138
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49. 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
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50. Dehdashti AR, Ganna A, Witterick I, Gentili F: Expanded endoscopic endonasal approach for anterior cranial base and suprasellar lesions: indications and limitations. Neurosurgery; 2009 Apr;64(4):677-87; discussion 687-9
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  • The introduction of endoscopy to transsphenoidal surgery, with its improved illumination and wider field of view, has added significant further potential for the resection of a variety of cranial base lesions.
  • METHODS: From June 2005 to June 2007, the expanded endoscopic endonasal approach was used in 22 patients with the following pathologies: 6 craniopharyngiomas; 4 esthesioneuroblastomas; 3 giant pituitary macroadenomas; 2 suprasellar Rathke's pouch cysts; 2 angiofibromas; and 1 each of suprasellar meningioma, germinoma, ethmoidal carcinoma, adenoid cystic carcinoma, and large suprasellar arachnoid cyst.

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  • (PMID = 19349826.001).
  • [ISSN] 1524-4040
  • [Journal-full-title] Neurosurgery
  • [ISO-abbreviation] Neurosurgery
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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51. Snyderman CH, Pant H, Carrau RL, Gardner P: A new endoscopic staging system for angiofibromas. Arch Otolaryngol Head Neck Surg; 2010 Jun;136(6):588-94
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [Title] A new endoscopic staging system for angiofibromas.
  • OBJECTIVE: To develop a new staging system for juvenile nasopharyngeal angiofibroma that reflects changes in surgical approaches (endonasal), route of intracranial extension, and the extent of vascular supply from the internal carotid artery.
  • PATIENTS: Patients undergoing endoscopic endonasal surgery for juvenile nasopharyngeal angiofibroma at the University of Pittsburgh Medical Center (UPMC), Pittsburgh, Pennsylvania, from 1998 through 2008.
  • CONCLUSIONS: Tumor size and extent of sinus disease are less important in predicting complete tumor removal with endonasal surgical techniques.
  • The UPMC staging system for juvenile nasopharyngeal angiofibroma accounts for 2 important prognostic factors, route of cranial base extension, and vascularity and is applicable to endoscopic or open approaches.
  • [MeSH-major] Angiofibroma / pathology. Endoscopy. Nasopharyngeal Neoplasms / pathology. Neoplasm Staging / standards


52. Anand V, Santosh S, Aishwarya A: Canine fossa approaches in endoscopic sinus surgery - our experience. Indian J Otolaryngol Head Neck Surg; 2008 Sep;60(3):214-7
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  • RESULT: Out of 1612 endoscopic sinus surgeries for various indications, CFA was used in 80 patients (4.96%) and among this 15 had bilateral procedure.The various diseases which required CFA were allergic fungal sinusitis (AFS), Fungal ball, Chronic invasive aspergillosis,antro choanal polyp, inflammatory polyp, Mucocoele and Maxillary cyst,inverted papilloma and Juvenile Nasopharyngeal Angiofibroma (JNA).

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  • (PMID = 23120545.001).
  • [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/ PMC3450635
  • [Keywords] NOTNLM ; ACP -Antro choanal Polyp / CFA - canine fossa approach / CRS - Chronic rhinosinusitis / FESS - Functional Endoscopic Sinus Surgery / IP-Inverted papilloma / JNA- Juvenile Nasopharyngeal Angiofibroma
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53. Dabholkar JP: Juvenile nasopharyngeal angiofibroma: clinical factors associated with recurrence and proposal of a staging system. J Surg Oncol; 2008 Aug 1;98(2):73
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  • [Title] Juvenile nasopharyngeal angiofibroma: clinical factors associated with recurrence and proposal of a staging system.
  • [MeSH-major] Angiofibroma / pathology. Angiofibroma / therapy. Nasopharyngeal Neoplasms / pathology. Nasopharyngeal Neoplasms / therapy. Neoplasm Recurrence, Local

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  • [CommentOn] J Surg Oncol. 2008 Aug 1;98(2):75-80 [18623038.001]
  • (PMID = 18623035.001).
  • [ISSN] 1096-9098
  • [Journal-full-title] Journal of surgical oncology
  • [ISO-abbreviation] J Surg Oncol
  • [Language] eng
  • [Publication-type] Comment; Editorial
  • [Publication-country] United States
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54. 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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  • [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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55. Marini F, Falchetti A, Del Monte F, Carbonell Sala S, Gozzini A, Luzi E, Brandi ML: Multiple endocrine neoplasia type 1. Orphanet J Rare Dis; 2006;1:38
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  • The sporadic form presents with two of the three principal MEN1-related endocrine tumours (parathyroid adenomas, entero-pancreatic tumours and pituitary tumours) within a single patient, while the familial form consists of a MEN1 case with at least one first degree relative showing one of the endocrine characterising tumours.
  • Other endocrine and non-endocrine lesions, such as adrenal cortical tumours, carcinoids of the bronchi, gastrointestinal tract and thymus, lipomas, angiofibromas, collagenomas have been described.
  • [MeSH-minor] Adolescent. Adrenal Cortex Neoplasms / diagnosis. Adult. Aged. Aged, 80 and over. Angiofibroma / diagnosis. Carcinoid Tumor / diagnosis. Child. Facial Neoplasms / diagnosis. Female. Gastrinoma / diagnosis. Genetic Testing / methods. Humans. Insulinoma / diagnosis. Lipoma / diagnosis. Male. Meningioma / diagnosis. Middle Aged. Prolactinoma / diagnosis. Proto-Oncogene Proteins / genetics. Thyroid Neoplasms / diagnosis. Vasoactive Intestinal Peptide / blood. Vasoactive Intestinal Peptide / secretion. Young Adult

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  • (PMID = 17014705.001).
  • [ISSN] 1750-1172
  • [Journal-full-title] Orphanet journal of rare diseases
  • [ISO-abbreviation] Orphanet J Rare Dis
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't; Review
  • [Publication-country] England
  • [Chemical-registry-number] 0 / MEN1 protein, human; 0 / Proto-Oncogene Proteins; 37221-79-7 / Vasoactive Intestinal Peptide
  • [Number-of-references] 64
  • [Other-IDs] NLM/ PMC1594566
  • [General-notes] NLM/ Original DateCompleted: 20070618
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56. Tang IP, Shashinder S, Gopala Krishnan G, Narayanan P: Juvenile nasopharyngeal angiofibroma in a tertiary centre: ten-year experience. Singapore Med J; 2009 Mar;50(3):261-4
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  • [Title] Juvenile nasopharyngeal angiofibroma in a tertiary centre: ten-year experience.
  • INTRODUCTION: This is a retrospective study that aimed to examine the outcomes of patients presenting with juvenile nasopharyngeal angiofibroma (JNA) at a tertiary centre in Malaysia.
  • One patient was at stage I, eight were at stage II, three at stage III and one patient was at stage IV, based on the Fisch classification.
  • CONCLUSION: JNA is a rare vascular benign tumour with highly exclusive persistence and recurrence, and typically affects adolescent boys.
  • [MeSH-major] Angiofibroma / diagnosis. Nasopharyngeal Neoplasms / diagnosis

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  • (PMID = 19352568.001).
  • [ISSN] 0037-5675
  • [Journal-full-title] Singapore medical journal
  • [ISO-abbreviation] Singapore Med J
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] Singapore
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57. Kapidzić A, Sutalo K: [Surgical treatment of juvenile nasopharyngeal angifibroma]. Med Arh; 2006;60(5):296-7
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  • [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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58. Gupta S, Bhowate R, Degwekar SS: Clinical and radiological findings related to tuberous sclerosis complex: a case report. J Contemp Dent Pract; 2008;9(4):85-91
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  • AIM: The aim of this report is to present the intraoral and extraoral clinical features of a young female patient with tuberous sclerosis complex (TSC) who exhibited multiple hamartomas of various organ systems including a fibromatous growth on the gingiva.
  • Associated findings were adenoma sebaceum (angiofibromas) on the face, a Shagreen patch on the lumbosacral region, ash leaf spots on the trunk, and subangual fibromas (Koenen's tumor) on the nails of fingers and toes.
  • The final diagnosis of TSC was made on the basis of the clinical findings of the skin, computerized tomography (CT) findings of the brain and kidney, ultrasonographic findings of kidney, and a histopathologic evaluation of the gingival growth which met the major and minor criteria required for a diagnosis of TSC.
  • The diagnosis and management of these patients varies depending on the specific presentation of the disease.
  • Dentists need to be mindful of the systemic issues as well as oral conditions related to this disease.
  • [MeSH-major] Gingival Diseases / diagnosis. Hamartoma / diagnosis. Tuberous Sclerosis / diagnosis
  • [MeSH-minor] Adolescent. Angiofibroma / diagnosis. Cuspid / pathology. Diagnosis, Differential. Facial Neoplasms / diagnosis. Female. Fibroma / diagnosis. Humans. Hyperpigmentation / diagnosis. Nail Diseases / diagnosis. Skin Neoplasms / diagnosis


59. Riggs S, Orlandi RR: Juvenile nasopharyngeal angiofibroma recurrence associated with exogenous testosterone therapy. Head Neck; 2010 Jun;32(6):812-5
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  • [Title] Juvenile nasopharyngeal angiofibroma recurrence associated with exogenous testosterone therapy.
  • BACKGROUND: Juvenile nasopharyngeal angiofibromas (JNAs) are rare benign lesions that express hormonal receptors.
  • This report describes a recurrence of a JNA 20 years after excision associated with exogenous testosterone therapy.
  • METHODS: A 36-year-old man developed a sphenoid mass 20 years following resection of a JNA, shortly after initiating exogenous testosterone therapy for symptomatic low endogenous testosterone.
  • [MeSH-major] Angiofibroma / physiopathology. Nasopharyngeal Neoplasms / physiopathology. Neoplasms, Second Primary / physiopathology. Paranasal Sinus Neoplasms / physiopathology. Sphenoid Sinus. Testosterone / physiology

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  • [Copyright] (c) 2009 Wiley Periodicals, Inc. Head Neck, 2010.
  • (PMID = 19626637.001).
  • [ISSN] 1097-0347
  • [Journal-full-title] Head & neck
  • [ISO-abbreviation] Head Neck
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 3XMK78S47O / Testosterone
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60. 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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  • [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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61. Momeni AJ, Roberts CC, Chew FS: Imaging of chronic and exotic sinonasal disease: self-assessment module. AJR Am J Roentgenol; 2007 Dec;189(6 Suppl):S46-8
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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 chronic and exotic sinonasal disease: self-assessment module.
  • This article focuses on the anatomy, pathophysiology, microbiology, and diagnosis of sinonasal disease, including chronic and fungal sinusitis, juvenile nasopharyngeal angiofibroma, inverted papilloma, and chondrosarcoma.
  • [MeSH-minor] Angiofibroma / pathology. Angiofibroma / radiography. Chondrosarcoma / pathology. Chondrosarcoma / radiography. Chronic Disease. Humans. Mycoses. Nasopharyngeal Neoplasms / pathology. Nasopharyngeal Neoplasms / radiography. Papilloma, Inverted / pathology. Papilloma, Inverted / radiography

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  • (PMID = 19642260.001).
  • [ISSN] 1546-3141
  • [Journal-full-title] AJR. American journal of roentgenology
  • [ISO-abbreviation] AJR Am J Roentgenol
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] United States
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62. Watanabe T, Yoshida Y, Yamamoto O: Angiomyofibroblastoma of the vulva with a penile appearance. Br J Dermatol; 2007 Jul;157(1):189-91
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Angiofibroma / pathology. Vulvar Neoplasms / pathology

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  • (PMID = 17578444.001).
  • [ISSN] 0007-0963
  • [Journal-full-title] The British journal of dermatology
  • [ISO-abbreviation] Br. J. Dermatol.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] England
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63. 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
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  • [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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64. Warraich I, Dunn DM, Oliver JW: Solitary fibrous tumor of the orbit with epithelioid features. Arch Pathol Lab Med; 2006 Jul;130(7):1039-41
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  • [Title] Solitary fibrous tumor of the orbit with epithelioid features.
  • Extrapleural solitary fibrous tumors have often been confused with other mesenchymal tumors, such as hemangiopericytoma, fibrous histiocytoma, fibrous meningioma, and leiomyoma, because of morphologic similarity and underrecognition, especially if some unusual features are present.
  • Recently, epithelioid solitary fibrous tumor has been reported in the mediastinum.
  • We report a case of solitary fibrous tumor of the orbit with biphasic architecture, including spindle cell and epithelioid components.
  • Both components demonstrated immunohistochemical features of a solitary fibrous tumor.
  • In this report, we discuss the differential diagnosis of solitary fibrous tumor with unusual epithelioid features.
  • Extrapleural solitary fibrous tumor should be included in the differential diagnosis of tumors of the orbit with a spindle cell appearance even in the presence of some epithelioid morphology.
  • [MeSH-major] Epithelioid Cells / pathology. Fibroma / pathology. Orbit / pathology. Orbital Neoplasms / pathology
  • [MeSH-minor] Aged. Angiofibroma / diagnosis. Biomarkers, Tumor / analysis. Diagnosis, Differential. Hemangiopericytoma / diagnosis. Histiocytoma, Benign Fibrous / diagnosis. Humans. Leiomyoma / diagnosis. Male. Meningioma / diagnosis. Neurilemmoma / diagnosis. Tomography, X-Ray Computed

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  • (PMID = 16831031.001).
  • [ISSN] 1543-2165
  • [Journal-full-title] Archives of pathology & laboratory medicine
  • [ISO-abbreviation] Arch. Pathol. Lab. Med.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
  • [Chemical-registry-number] 0 / Biomarkers, Tumor
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65. Cai T, Zhou B, Huang Q, Liang X, Ni X, Cui S, Li Y, Wang T, Zang H, Liu H, Liu M, Han D: [Analysis of prognostic factors in endoscopic surgery for juvenile nasopharyngeal angiofibroma]. Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2010 Nov;24(22):1035-9
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  • [Title] [Analysis of prognostic factors in endoscopic surgery for juvenile nasopharyngeal angiofibroma].
  • OBJECTIVE: Analyzing the prognostic factors in endoscopic surgery of juvenile nasopharyngeal angiofibromas (JNA).
  • [MeSH-major] Angiofibroma / diagnosis. Nasopharyngeal Neoplasms / diagnosis

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  • (PMID = 21322931.001).
  • [ISSN] 1001-1781
  • [Journal-full-title] Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery
  • [ISO-abbreviation] Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] China
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66. Barat S, Tirgar-Tabari S, Shafaee S: Angiomyofibroblastoma of the vulva. Arch Iran Med; 2008 Mar;11(2):224-6
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  • Angiomyofibroblastoma is a benign well-circumscribed tumor characterized by alternating hypocellular and hypercellular areas with abundant thin-walled blood vessels.
  • [MeSH-major] Angiofibroma / diagnosis. Angiomyoma / diagnosis. Vulvar Neoplasms / diagnosis

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  • (PMID = 18298306.001).
  • [ISSN] 1029-2977
  • [Journal-full-title] Archives of Iranian medicine
  • [ISO-abbreviation] Arch Iran Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Iran
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67. Mohammadi M, Saedi B, Basam A: Effect of embolisation on endoscopic resection of angiofibroma. J Laryngol Otol; 2010 Jun;124(6):631-5
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  • [Title] Effect of embolisation on endoscopic resection of angiofibroma.
  • OBJECTIVE: To determine the effect of embolisation on endoscopic resection of angiofibroma.
  • Twenty-three patients with angiofibroma (nine embolised and 14 not embolised) underwent endoscopic resection between January 2007 and August 2008 in two tertiary referral centres.
  • CONCLUSION: Endoscopic resection is a feasible and safe method for angiofibroma surgery.
  • The current evidence does not support obligatory embolisation in every case of endoscopic angiofibroma resection.
  • [MeSH-major] Angiofibroma / surgery. Blood Loss, Surgical / prevention & control. Embolization, Therapeutic. Endoscopy / methods. Nasopharyngeal Neoplasms / surgery

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  • (PMID = 20067650.001).
  • [ISSN] 1748-5460
  • [Journal-full-title] The Journal of laryngology and otology
  • [ISO-abbreviation] J Laryngol Otol
  • [Language] eng
  • [Publication-type] Journal Article; Multicenter Study; Randomized Controlled Trial; Research Support, Non-U.S. Gov't
  • [Publication-country] England
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68. Tandon A, Branson HM, Buncic JR: Transient visual loss and isolated disk edema in juvenile nasopharyngeal angiofibroma. J AAPOS; 2010 Feb;14(1):90-2
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  • [Title] Transient visual loss and isolated disk edema in juvenile nasopharyngeal angiofibroma.
  • Juvenile nasopharyngeal angiofibroma is a well-described but rare benign tumor that mainly affects adolescent boys.

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  • [Copyright] Copyright (c) 2010 American Association for Pediatric Ophthalmology and Strabismus. Published by Mosby, Inc. All rights reserved.
  • (PMID = 20045362.001).
  • [ISSN] 1528-3933
  • [Journal-full-title] Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
  • [ISO-abbreviation] J AAPOS
  • [Language] ENG
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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69. Chtourou I, Bahri Zouari I, Hammami S, Gouiaa N, Khabir A, Ayadi L, Boudawara TS: [An exceptional cause of inguinal hernia]. Ann Pathol; 2007 Apr;27(2):149-51
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  • [Transliterated title] Une étiologie exceptionnelle de hernie inguinale.
  • [MeSH-major] Abdominal Neoplasms / complications. Angiofibroma / complications. Hernia, Inguinal / etiology. Inguinal Canal

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  • (PMID = 17909478.001).
  • [ISSN] 0242-6498
  • [Journal-full-title] Annales de pathologie
  • [ISO-abbreviation] Ann Pathol
  • [Language] fre
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] France
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70. Pires CF, Anunciação GM, De Sousa WL, Santos BM, Anunciação FA, Pires AF, Pires LF: [Tuberous sclerosis in childhood]. Dermatol Online J; 2008;14(9):14
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  • Tuberous sclerosis is an autosomal dominant disease that results from mutations in one of two tumor suppressor genes, TSC1 and TSC2.
  • We are reporting a two-year-old girl who presented with hypopigmented macules (ash leaf) in the skin and small erythematous facial papules (angiofibromas).
  • Although the signs of tuberous sclerosis were specifically looked for in this patient because of her mother, subtle angiofibromas in a young child can be easily missed.
  • [MeSH-major] Angiofibroma / etiology. Facial Neoplasms / etiology. Tuberous Sclerosis / diagnosis


71. Cariappa KM, Sethi A, Srikanth G, Kumar R: Juvenile nasopharyngeal angiofibroma presenting as an intraoral mass. Br J Oral Maxillofac Surg; 2008 Oct;46(7):578
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  • [Title] Juvenile nasopharyngeal angiofibroma presenting as an intraoral mass.
  • [MeSH-major] Angiofibroma / diagnosis. Nasopharyngeal Neoplasms / diagnosis. Palatal Neoplasms / diagnosis

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  • (PMID = 18448214.001).
  • [ISSN] 1532-1940
  • [Journal-full-title] The British journal of oral & maxillofacial surgery
  • [ISO-abbreviation] Br J Oral Maxillofac Surg
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Scotland
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72. 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
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  • [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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73. Das S, Kirsch CF: Imaging of lumps and bumps in the nose: a review of sinonasal tumours. Cancer Imaging; 2005;5:167-77
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  • 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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74. Kozovski G, Angelova M: [The Morris syndrome. Case report]. Akush Ginekol (Sofiia); 2007;46(8):43-4
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-minor] Adult. Angiofibroma / pathology. Angiofibroma / surgery. Angiofibroma / ultrasonography. Female. Genitalia, Female / ultrasonography. Humans. Laparoscopy. Male. Testicular Neoplasms / pathology. Testicular Neoplasms / surgery. Testicular Neoplasms / ultrasonography. Testis / pathology. Testis / surgery. Testis / ultrasonography

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  • (PMID = 18649406.001).
  • [ISSN] 0324-0959
  • [Journal-full-title] Akusherstvo i ginekologii︠a︡
  • [ISO-abbreviation] Akush Ginekol (Sofiia)
  • [Language] bul
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Bulgaria
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75. Pérez-Navarro JV, Flores-Cardoza A, Anaya-Prado R, González-Izquierdo Jde J, Ramírez-Barba EJ: [Angiofibrolipoma of the greater omentum: case report and literature review]. Cir Cir; 2009 May-Jun;77(3):229-32
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  • [Transliterated title] Angiofibrolipoma de omento mayor. Informe de un caso y revisión de la literatura.
  • Lipomas, leiomyomas, fibromas, and neurofibromas have been described as benign tumors of the greater omentum, but angiofibrolipomas have not.
  • CLINICAL CASE: We present the case of a 39-year-old male with a 3-day evolution of right lower quadrant abdominal pain associated with nausea and vomiting.
  • [MeSH-major] Angiofibroma. Angiolipoma. Omentum. Peritoneal Neoplasms

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  • (PMID = 19671276.001).
  • [ISSN] 0009-7411
  • [Journal-full-title] Cirugía y cirujanos
  • [ISO-abbreviation] Cir Cir
  • [Language] spa
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Mexico
  • [Number-of-references] 22
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76. Koo PJ, Goykhman I, Lembert L, Nunes LW: MRI features of cellular angiomyofibroma with pathologic correlation. J Magn Reson Imaging; 2009 May;29(5):1195-8
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  • Within the spectrum of extratesticular mesenchymal tumors in the scrotum and perineum lies cellular angiofibroma, also known as angiomyofibroblastoma-like tumor, a rare lesion originally described to almost exclusively occur in the vulva, perineum, and pelvis of women.
  • We present the MRI features of cellular angiofibroma that are consistent with the pathological characteristics of this entity-a benign cellular and fibrous tumor with prominent vascularity.

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  • (PMID = 19388110.001).
  • [ISSN] 1053-1807
  • [Journal-full-title] Journal of magnetic resonance imaging : JMRI
  • [ISO-abbreviation] J Magn Reson Imaging
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] United States
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77. Sakurai A, Hashizume K, Fukushima Y: Facial angiofibroma as an initial manifestation in multiple endocrine neoplasia type 1. Intern Med; 2008;47(11):1067-8
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  • [Title] Facial angiofibroma as an initial manifestation in multiple endocrine neoplasia type 1.
  • [MeSH-major] Angiofibroma / pathology. Facial Neoplasms / pathology. Multiple Endocrine Neoplasia Type 1 / diagnosis


78. 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
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  • [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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79. Stewart C: Angiomyofibroblastoma of the vagina. Pathology; 2009 Feb;41(2):199-200; author reply 200-1
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Angiofibroma / pathology. Angiomyoma / pathology. Breast Neoplasms / pathology. Neoplasms, Muscle Tissue / pathology. Neoplasms, Second Primary / pathology. Vaginal Neoplasms / pathology

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  • [CommentOn] Pathology. 2008 Aug;40(5):534-6 [18604746.001]
  • (PMID = 19152197.001).
  • [ISSN] 0031-3025
  • [Journal-full-title] Pathology
  • [ISO-abbreviation] Pathology
  • [Language] eng
  • [Publication-type] Comment; Letter
  • [Publication-country] England
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80. 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
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  • [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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81. Lehnerdt G, Oztürk E, Grabellus F: [Gigantic nasal tumor]. HNO; 2009 Apr;57(4):368-70
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  • A space-occupying lesion, which had been growing on the external surface of the nose of a 57-year-old man for 5 years was considered to most likely be an angiofibroma after surgical removal and histological examination, but the final clinical diagnosis was clearly a rhinophyma.
  • [MeSH-major] Angiofibroma / pathology. Angiofibroma / surgery. Nose Neoplasms / pathology. Nose Neoplasms / surgery. Rhinophyma / pathology. Rhinophyma / surgery

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  • [Cites] Facial Plast Surg. 1998;14(4):241-53 [11816064.001]
  • [Cites] Ann Plast Surg. 2008 Jul;61(1):114-20 [18580161.001]
  • [Cites] HNO. 1997 Aug;45(8):636-7 [9378671.001]
  • (PMID = 19183915.001).
  • [ISSN] 1433-0458
  • [Journal-full-title] HNO
  • [ISO-abbreviation] HNO
  • [Language] ger
  • [Publication-type] Case Reports; English Abstract; Journal Article
  • [Publication-country] Germany
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82. 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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83. Biswas D, Saha S, Bera SP: Relative distribution of the tumours of ear, nose and throat in the paediatric patients. Int J Pediatr Otorhinolaryngol; 2007 May;71(5):801-5
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  • The ratio of benign to malignant lesion was 7.6:1.
  • Juvenile nasopharyngeal angiofibroma was the commonest tumour (11 cases, 26%) and embryonal rhabdomyosarcoma was the commonest malignant tumour (3 cases, 7%).
  • This study indicates that the distribution of otolaryngological tumours in the Indian subcontinent is different from the western countries, particularly the juvenile nasopharyngeal angiofibroma and laryngeal papilloma.

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  • (PMID = 17368816.001).
  • [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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84. Pryor SG, Moore EJ, Kasperbauer JL: Endoscopic versus traditional approaches for excision of juvenile nasopharyngeal angiofibroma. Laryngoscope; 2005 Jul;115(7):1201-7
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  • [Title] Endoscopic versus traditional approaches for excision of juvenile nasopharyngeal angiofibroma.
  • OBJECTIVES: Juvenile nasopharyngeal angiofibroma (JNA) is an uncommon neoplasm originating in the nasopharynx.
  • [MeSH-major] Angiofibroma / surgery. Endoscopy / methods. Nasopharyngeal Neoplasms / surgery. Otorhinolaryngologic Surgical Procedures / methods

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  • (PMID = 15995507.001).
  • [ISSN] 0023-852X
  • [Journal-full-title] The Laryngoscope
  • [ISO-abbreviation] Laryngoscope
  • [Language] eng
  • [Publication-type] Comparative Study; Journal Article
  • [Publication-country] United States
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85. Korol UB, Schoor R, Nanda V, Almas K, Phelan JA: Gingival enlargement as a manifestation of tuberous sclerosis: case report and periodontal management. J Periodontol; 2008 Apr;79(4):759-63
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  • BACKGROUND: Tuberous sclerosis is an autosomal-dominant inherited disease involving many organs of the body.
  • Oral manifestations include gingival enlargement, fibromas, and dental enamel pitting.
  • The report presents a case of tuberous sclerosis with gingival enlargement histologically consistent with angiofibroma, describes its successful periodontal management, and reviews the literature associated with oral manifestations of tuberous sclerosis.
  • RESULTS: Histologic examination of the gingival tissue revealed features consistent with angiofibroma.
  • CONCLUSIONS: The gingival enlargement was histologically consistent with the characteristic angiofibromas of tuberous sclerosis.
  • [MeSH-minor] Adult. Angiofibroma / pathology. Debridement. Dental Scaling. Follow-Up Studies. Gingival Neoplasms / pathology. Gingivectomy. Humans. Male. Toothbrushing

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  • (PMID = 18380572.001).
  • [ISSN] 0022-3492
  • [Journal-full-title] Journal of periodontology
  • [ISO-abbreviation] J. Periodontol.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Review
  • [Publication-country] United States
  • [Number-of-references] 30
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86. 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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  • [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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87. 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
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  • [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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88. Antoniv VF, Shakhverdiev AK, Antoniv TV, Pushkar' IS: [Otalgia and impairment of hearing in the diagnosis of inflammatory and tumorous diseases of the pharynx and larynx]. Vestn Otorinolaringol; 2010;(2):11-3
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  • [Title] [Otalgia and impairment of hearing in the diagnosis of inflammatory and tumorous diseases of the pharynx and larynx].
  • A total of 1074 patients with pharyngeal and laryngeal problems were available for examination that revealed pathologies in which otalgia and/or impairment of hearing is the first or an earlier symptom of the disease.
  • Otalgia proved to be an early manifestation of serious inflammatory diseases affecting the middle part of the pharynx or of metastasis of malignant pharyngeal and laryngeal tumours into deep cervical lymph nodes.
  • Juvenile angiofibroma, hemangiouma, malignant nasopharyngeal tumour are known to disturb functional automatism of pharyngeal openings of Eustachian tubes and cause impairment of hearing long before clinical manifestations of neoplastic growth.

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  • (PMID = 20517271.001).
  • [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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89. Sakamoto A, Weinstein LS, Plagge A, Eckhaus M, Kelsey G: GNAS haploinsufficiency leads to subcutaneous tumor formation with collagen and elastin deposition and calcification. Endocr Res; 2009;34(1-2):1-9
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  • We now describe the development of fibrous tumors in mice with heterozygous disruption of the Gnas gene, which encodes G(s)alpha and other gene products.
  • METHODS AND RESULTS: Disruption of Gnas exon 2 on either the maternal or paternal allele (Gnas(E2-/+)) results in fibromas or angiofibromas on the ears, paws and tail beginning at 4 months of age.
  • [MeSH-major] Angiofibroma / genetics. Collagen / metabolism. Elastin / metabolism. Fibroma / genetics. GTP-Binding Protein alpha Subunits, Gs / genetics. Skin Neoplasms / genetics

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  • (PMID = 19557586.001).
  • [ISSN] 1532-4206
  • [Journal-full-title] Endocrine research
  • [ISO-abbreviation] Endocr. Res.
  • [Language] eng
  • [Grant] United States / Intramural NIH HHS / / Z01 DK043302-14
  • [Publication-type] Journal Article; Research Support, N.I.H., Intramural
  • [Publication-country] England
  • [Chemical-registry-number] 9007-34-5 / Collagen; 9007-58-3 / Elastin; EC 3.6.1.- / Gnas protein, mouse; EC 3.6.5.1 / GTP-Binding Protein alpha Subunits, Gs
  • [Other-IDs] NLM/ NIHMS79043; NLM/ PMC2702697
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90. Margalit N, Wasserzug O, De-Row A, Abergel A, Fliss DM, Gil Z: Surgical treatment of juvenile nasopharyngeal angiofibroma with intracranial extension. Clinical article. J Neurosurg Pediatr; 2009 Aug;4(2):113-7
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  • [Title] Surgical treatment of juvenile nasopharyngeal angiofibroma with intracranial extension. Clinical article.
  • OBJECT: The purpose of this study was to describe the surgical treatment and outcomes of patients with intracranial extension of juvenile nasopharyngeal angiofibroma (JNA).
  • [MeSH-major] Angiofibroma / pathology. Angiofibroma / surgery. Nasopharyngeal Neoplasms / pathology. Nasopharyngeal Neoplasms / surgery

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  • [CommentIn] J Neurosurg Pediatr. 2012 Mar;9(3):336-7; author reply 337 [22380966.001]
  • (PMID = 19645542.001).
  • [ISSN] 1933-0707
  • [Journal-full-title] Journal of neurosurgery. Pediatrics
  • [ISO-abbreviation] J Neurosurg Pediatr
  • [Language] eng
  • [Publication-type] Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] United States
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91. 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
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  • [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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92. Gull S, Badawy A, Chaudhuri A: The 'pulsatile' sebaceous cyst: beware of a superficial temporal artery aneurysm. BMJ Case Rep; 2009;2009
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  • [Title] The 'pulsatile' sebaceous cyst: beware of a superficial temporal artery aneurysm.
  • Other conditions to be included in the differential diagnosis are haematoma, angiofibroma, eroding middle meningeal artery aneurysm, abscess or a parotid mass.

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  • [ISSN] 1757-790X
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  • [ISO-abbreviation] BMJ Case Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC3028217
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93. Liu QL, Tian B, Zhang H, Qiao DS: Angiofibrolipoma of the spermatic cord. Asian J Androl; 2009 Nov;11(6):746-7
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • [MeSH-major] Angiofibroma / pathology. Genital Neoplasms, Male / pathology. Lipoma / pathology. Spermatic Cord / pathology

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  • [ISSN] 1745-7262
  • [Journal-full-title] Asian journal of andrology
  • [ISO-abbreviation] Asian J. Androl.
  • [Language] eng
  • [Publication-type] Case Reports; Letter
  • [Publication-country] China
  • [Other-IDs] NLM/ PMC3735332
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94. Shu HR, Yang QT, Lai YY, Mo JG, Mao WH, Song JX, Zheng GJ: Giant cell angiofibroma in the vocal cord. Chin Med J (Engl); 2010 Dec;123(23):3479-81
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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 in the vocal cord.
  • [MeSH-major] Angiofibroma / pathology. Giant Cell Tumors / pathology. Laryngeal Neoplasms / pathology. Vocal Cords

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  • (PMID = 22166534.001).
  • [ISSN] 0366-6999
  • [Journal-full-title] Chinese medical journal
  • [ISO-abbreviation] Chin. Med. J.
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article; Research Support, Non-U.S. Gov't
  • [Publication-country] China
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95. 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
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  • [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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  • (PMID = 18706100.001).
  • [ISSN] 1752-1947
  • [Journal-full-title] Journal of medical case reports
  • [ISO-abbreviation] J Med Case Rep
  • [Language] eng
  • [Publication-type] Journal Article
  • [Publication-country] England
  • [Other-IDs] NLM/ PMC2535598
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96. 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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97. Pellegrino M, Vadrucci S, Tinelli A: [Angiomyofibroblastoma of the vulva: a rare but distinct entity. Case report and literature review]. Pathologica; 2007 Dec;99(6):438-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Angiomyofibroblastoma is a benign vulvar tumour involving soft tissue that is characterized by alternating hypocellular and hypercellular areas of spindle stromal cells, admixed and aggregated around blood vessels.
  • It is important to recognize this entity as it shows benign behaviour with respect to other mesenchymal tumours of the vagina, which have a more aggressive behaviour.
  • [MeSH-major] Angiofibroma / pathology. Angiomyoma / pathology. Hemangioblastoma / pathology. Neoplasms, Second Primary / pathology. Vulvar Neoplasms / pathology

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  • (PMID = 18416337.001).
  • [ISSN] 0031-2983
  • [Journal-full-title] Pathologica
  • [ISO-abbreviation] Pathologica
  • [Language] ita
  • [Publication-type] Case Reports; English Abstract; Journal Article; Review
  • [Publication-country] Italy
  • [Chemical-registry-number] 0 / Antigens, CD34; 0 / Biomarkers, Tumor; 0 / Neoplasm Proteins; 0 / Receptors, Estrogen
  • [Number-of-references] 7
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98. Chen H, Sun XF, Wu JS: [Clinicopathologic study of subependymal giant cell astrocytoma]. Zhonghua Bing Li Xue Za Zhi; 2006 Nov;35(11):656-9
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • Eleven patients (61.1%) had clinical features of tuberous sclerosis, usually in the form of facial angiofibroma (8/18, 44.4%).
  • CONCLUSIONS: Subependymal giant cell astrocytoma is a benign brain tumor with distinctive histopathologic features.

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  • (PMID = 17374208.001).
  • [ISSN] 0529-5807
  • [Journal-full-title] Zhonghua bing li xue za zhi = Chinese journal of pathology
  • [ISO-abbreviation] Zhonghua Bing Li Xue Za Zhi
  • [Language] chi
  • [Publication-type] English Abstract; Journal Article
  • [Publication-country] China
  • [Chemical-registry-number] 0 / Glial Fibrillary Acidic Protein; 0 / Synaptophysin
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99. Muhammed K, Mathew J: Coexistence of two neurocutaneous syndromes: tuberous sclerosis and hypomelanosis of Ito. Indian J Dermatol Venereol Leprol; 2007 Jan-Feb;73(1):43-5
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • He also had facial angiofibromas, ash-leaf and confetti macules and shagreen patches.
  • [MeSH-minor] Angiofibroma / complications. Brain / pathology. Child, Preschool. Epilepsy / complications. Facial Neoplasms / complications. Humans. Intellectual Disability / complications. Magnetic Resonance Imaging. Male


100. Altraide DD, George IO, Otike-Odibe B: Tuberous sclerosis: a rare cause of seizure in Nigeria. Niger J Med; 2010 Jul-Sep;19(3):326-8
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  • [Source] The source of this record is MEDLINE®, a database of the U.S. National Library of Medicine.
  • BACKGROUND: Tuberous sclerosis is a rare genetic multisystem disorder that is typically apparent shortly after birth.
  • Dermatologic manifestations may be the only clues to the diagnosis of the disorder, which is also marked by childhood seizures and mental retardation.
  • METHODS: A review of the case records of a child with angiofibromas of the face and neck and the relevant literature.
  • Physical examination showed that he had labile mood with presence of hyperpigmented papulonodular (angiofibromas) eruptions on the malar area of the face and neck.
  • He is being managed by a team of a paediatric neurologist, surgeon, speech therapist and a dermatologist.
  • [MeSH-minor] Analgesics, Non-Narcotic / therapeutic use. Carbamazepine / therapeutic use. Child. Humans. Male. Nigeria. Parietal Lobe / radiography. Skin Diseases / etiology. Tomography, X-Ray Computed. Treatment Outcome

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  • (PMID = 20845641.001).
  • [ISSN] 1115-2613
  • [Journal-full-title] Nigerian journal of medicine : journal of the National Association of Resident Doctors of Nigeria
  • [ISO-abbreviation] Niger J Med
  • [Language] eng
  • [Publication-type] Case Reports; Journal Article
  • [Publication-country] Nigeria
  • [Chemical-registry-number] 0 / Analgesics, Non-Narcotic; 33CM23913M / Carbamazepine
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