中耳唾液腺瘤:一例罕见病例报告及先天性关联、面神经受累及治疗策略的最新进展。

IF 0.4 Q4 OTORHINOLARYNGOLOGY
Case Reports in Otolaryngology Pub Date : 2020-08-24 eCollection Date: 2020-01-01 DOI:10.1155/2020/8435140
Allen Young, Lauran Evans, Matthew Ng
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引用次数: 4

摘要

唾液腺绒毛瘤是一种极为罕见的中耳肿块,被认为是由第二鳃弓发育异常引起的。我们报告一名14岁的女孩患有丹迪-沃克综合征和传导性听力损失。中耳探查发现一大块中耳肿块,无母耳和镫骨,面神经移位。肿物完全切除,组织学证实为唾液腺绒毛瘤。骨锚式助听器(BAHA)改善了她的听力。由于面神经受累是常见的,医生应考虑部分切除以避免面神经麻痹。听力恢复可以通过OCR或BAHA来实现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Middle Ear Salivary Choristoma: A Rare Case Report and Update on Congenital Associations, Facial Nerve Involvement, and Treatment Strategies.

Middle Ear Salivary Choristoma: A Rare Case Report and Update on Congenital Associations, Facial Nerve Involvement, and Treatment Strategies.

Middle Ear Salivary Choristoma: A Rare Case Report and Update on Congenital Associations, Facial Nerve Involvement, and Treatment Strategies.

Middle Ear Salivary Choristoma: A Rare Case Report and Update on Congenital Associations, Facial Nerve Involvement, and Treatment Strategies.

Salivary gland choristoma is an extremely rare middle ear mass and is hypothesized to be caused by second branchial arch developmental anomalies. We present a 14-year-old girl with Dandy-Walker syndrome and conductive hearing loss. Middle ear exploration revealed a large middle ear mass with absent incus and stapes and displaced facial nerve. The mass was completely excised with histological confirmation of salivary gland choristoma. Her hearing was improved with bone-anchored hearing aids (BAHA). As facial nerve involvement is common, physicians should consider partial excision to avoid facial nerve palsy. Hearing restoration can be achieved with OCR or BAHA.

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来源期刊
Case Reports in Otolaryngology
Case Reports in Otolaryngology OTORHINOLARYNGOLOGY-
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审稿时长
13 weeks
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