2005
DOI: 10.1016/j.amjoto.2004.08.012
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Nasopharyngeal angiofibroma in an elderly woman

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Cited by 46 publications
(30 citation statements)
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“…2 A few cases have been reported in men over 25 years and in female teenagers. [3][4][5] It is thought that the anatomical origin of this tumor is the postero/lateral wall of the nasal cavity, close to the superior border of the sphenopalatine foramen. This tumor starts to grow on the submucosa of the floor of the nasopharynx, reaching the nasal septum and the posterior space of the nose, thereby causing a mass effect that may lead to airway obstruction.…”
Section: Introductionmentioning
confidence: 99%
“…2 A few cases have been reported in men over 25 years and in female teenagers. [3][4][5] It is thought that the anatomical origin of this tumor is the postero/lateral wall of the nasal cavity, close to the superior border of the sphenopalatine foramen. This tumor starts to grow on the submucosa of the floor of the nasopharynx, reaching the nasal septum and the posterior space of the nose, thereby causing a mass effect that may lead to airway obstruction.…”
Section: Introductionmentioning
confidence: 99%
“…[6] Juvenil nazofarengeal anjiofibromun etyopatogenezini açıklamak için farklı teoriler ileri sürülmüştür. [7] Bu teorileri dört ana kategoride toplamak mümkündür;…”
Section: Discussionunclassified
“…Buna rağ-men literatürde bildirilmiş kadın olgular da bulunmaktadır. [6][7][8][9][10] Bizim çalışmamızda da bir kadın hasta yer almaktadır. Kadın hastalarda JNA tanısı histopatolojik olarak doğrulandığın-da seks kromozom anomalileri araştırılmalıdır.…”
Section: Discussionunclassified
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“…Further, the association of NAF with familial adenomatous polyposis, in which the prevalence of NAF is 25 times more common than in age-matched controls [15], has not been confirmed in this case series. We consider that NAF occurs exclusively in males, and previous reports in females probably do not represent this tumor, or at least, documentation is not convincing [16][17][18][19]. In 1965, Apostol and Frazell [20] reported 40 cases of NAF in male patients, and suggested that if this diagnosis is confirmed in a female, sex chromosome studies must be performed, to investigate for androgen insensitivity syndrome (formerly testicular feminization) of a phenotypic female but genetic male [18,20].…”
Section: Discussionmentioning
confidence: 99%