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双侧先天性胆脂瘤。

Bilateral congenital cholesteatomas.

作者信息

Braganza R A, Kearns D B

机构信息

Division of Head and Neck Surgery, University of California, San Diego.

出版信息

Am J Otol. 1993 Mar;14(2):191-3.

PMID:8503497
Abstract

Congenital cholesteatoma is a rare entity. Bilateral involvement is rarer still. We present the sixth case of bilateral congenital cholesteatoma and briefly review the theories regarding the origin of congenital cholesteatoma. The lesion in the left ear was seen on physical examination, however the lesion in the right ear was detected only on a computed tomography (CT) scan, which was obtained to assess the extent of the disease on the left side. Although usually asymptomatic, these cholesteatomas can enlarge and lead to complications. Management of congenital cholesteatoma by various surgical approaches is discussed.

摘要

先天性胆脂瘤是一种罕见的疾病。双侧受累更为罕见。我们报告第六例双侧先天性胆脂瘤病例,并简要回顾关于先天性胆脂瘤起源的理论。左耳病变通过体格检查发现,然而右耳病变仅在计算机断层扫描(CT)中检测到,该扫描是为了评估左侧疾病的范围而进行的。尽管这些胆脂瘤通常无症状,但可增大并导致并发症。本文讨论了通过各种手术方法治疗先天性胆脂瘤的情况。

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