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中耳涎腺迷离瘤:1例报告并文献复习

Salivary gland choristoma of the middle ear: report of a case and review of the literature.

作者信息

Hinni M L, Beatty C W

机构信息

Department of Otolaryngology, Mayo Clinic Scottsdale, AZ 85259, USA.

出版信息

Ear Nose Throat J. 1996 Jul;75(7):422-4.

PMID:8764703
Abstract

Salivary gland choristoma (heterotopic salivary gland tissue) is a rare condition that occurs at various locations within the head and neck. We present a 10-year-old boy with a salivary gland choristoma of the middle ear and compare findings with the 15 similar cases published in the English and German languages. Patients typically have a long-standing conductive hearing loss and visible middle ear mass. Operative findings include a lobulated middle ear mass of histologically normal salivary gland tissue attached posteriorly in the region of the oval window, together with absent or malformed ossicles. Frequently the mass is intimately associated with the facial nerve. The constancy of these findings has led to the proposal of an abnormal developmental syndrome. This syndrome will be described and possible explanations for its cause will be discussed.

摘要

涎腺迷离瘤(异位涎腺组织)是一种罕见病症,发生于头颈部的不同部位。我们报告一名患有中耳涎腺迷离瘤的10岁男孩,并将其检查结果与以英文和德文发表的15例类似病例进行比较。患者通常有长期的传导性听力损失和可见的中耳肿物。手术所见包括一个分叶状的中耳肿物,由组织学上正常的涎腺组织构成,附着于椭圆窗区域后方,同时伴有听小骨缺失或畸形。肿物常常与面神经紧密相连。这些发现的一致性促使人们提出一种异常发育综合征。本文将描述这种综合征,并讨论其可能的病因解释。

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