【先天性中耳胆脂瘤伴外耳道全闭锁2例】。

Q3 Medicine
I A Anikin, N N Khamgushkeeva, A D Knyazev, A D Mamedova
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引用次数: 0

摘要

先天性外耳道狭窄和闭锁是最常见的外耳发育异常。这些畸形合并颞骨胆脂瘤的病例在世界文献中已被反复报道。这种合并病理更典型的先天性外耳道狭窄。外耳道完全闭锁很少与胆脂瘤有关。在锁骨板后发现的胆脂瘤被归类为先天性的,排除了它形成的其他可能机制。本文报告两例先天性胆脂瘤合并外耳道完全闭锁的临床病例:一名8岁女孩和一名19岁男孩,未发生颞内和颞外并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Congenital cholesteatoma of the middle ear with total atresia of the external auditory canal: two cases report].

Congenital stenosis and atresia of the external auditory canal are the most common developmental anomalies of the external ear. Cases of combination of these malformations with cholesteatoma of the temporal bone have been repeatedly described in the world literature. This combined pathology is more typical of congenital stenosis of the external auditory canal. Total atresia of the external auditory canal is rarely associated with cholesteatoma. Cholesteatoma found behind the atretic plate is classified as congenital, excluding other possible mechanisms of it's formation. The article presents two clinical cases of a combination of congenital cholesteatoma and complete atresia of the external auditory canal: in an 8-year old girl and a 19-year old boy without the development of intratemporal and extratemporal complications.

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来源期刊
Vestnik otorinolaringologii
Vestnik otorinolaringologii Medicine-Otorhinolaryngology
CiteScore
0.80
自引率
0.00%
发文量
69
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