儿童胆脂瘤的解剖和手术特点。

B Raffin, G Lacher, F Devars, C Benassayag, P Boudard, L Traissac
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引用次数: 1

摘要

在儿童中,胆脂瘤与咽鼓管功能障碍密切相关,并在可延性颞骨内发展。这类患者的听觉和语言功能的重要性使我们使用了一种非常特殊的临床哲学。目前我们研究了154例15岁以下儿童胆脂瘤。以下三点已经被证明:胆脂瘤的发病机制可以是原发性的,继发性的(由于收缩袋的不利延伸或鳞状细胞的迁移),甚至是医源性的;解剖和临床表现(x线检查)预测所采用的治疗方法;外科治疗通常需要“重新审视”手术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anatomical and surgical particularities of cholesteatomas in children.

In children, cholesteatoma is closely related to dysfunction of the eustachian tube and evolves inside a malleable temporal bone. The importance of auditory and speech functions in such patients has caused us to use a very particular clinical philosophy. At the present time we have studied 154 cases of cholesteatomas in children under 15 years old. The following three points have been shown: the pathogenesis of a cholesteatoma can be of the primary type, secondary (due to an unfavorable extension of retraction pocket or to squamous cell migration) or even be iatrogenic; anatomical and clinical findings (with X-ray studies) predicate the treatment used; surgical treatment frequently requires a "second-look" operation.

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