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Salivary Gland Choristoma in External Auditory Canal: A Case Report
Fetal and Pediatric Pathology ( IF 0.7 ) Pub Date : 2022-04-05 , DOI: 10.1080/15513815.2022.2059603
Vijayashree Raghavan 1 , Pooja E Moorthy 1 , Sudha Srinivasan 1
Affiliation  

Abstract

Introduction

Salivary gland choristomas have been described in the middle ear but tend not to involve the external auditory canal.

Case presentation

A 6-year-old boy with situs inversus totalis presented with congenital hearing loss in the left ear due to external auditory canal atresia. High resolution computed tomography of the temporal bone demonstrated a soft tissue obstruction of the external auditory canal with a normal middle ear. Histopathologically, this was a salivary gland choristoma. Post operatively the patient had a facial nerve palsy.

Conclusion

Salivary gland choristomas of middle ear have been reported, but have not been described with external auditory canal atresia and situs inversus totalis.



中文翻译:

外耳道唾液腺迷离瘤一例

摘要

介绍

已在中耳描述了唾液腺迷离瘤,但往往不累及外耳道。

案例展示

一名 6 岁患有全内翻的男孩因外耳道闭锁导致左耳先天性听力损失。颞骨高分辨率计算机断层扫描显示外耳道软组织阻塞,中耳正常。组织病理学上,这是一个唾液腺迷雾瘤。术后患者出现面神经麻痹。

结论

中耳唾液腺迷走神经瘤已有报道,但未见外耳道闭锁和全内反位的报道。

更新日期:2022-04-05
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