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喉表皮样囊肿:1例罕见病例报告及文献复习

Laryngeal epidermal inclusion cyst: report of an unusual case and literature review.

作者信息

Khushaim Hanan, Albaghli Slava, Al-Alsheikh Abdulmalik, Al Rikabi Ammar

机构信息

Anatomic Pathology, King Saud University, Riyadh, Saudi Arabia.

出版信息

J Surg Case Rep. 2020 Nov 30;2020(11):rjaa488. doi: 10.1093/jscr/rjaa488. eCollection 2020 Nov.

Abstract

The causes of dysphonia or hoarseness are numerous and can be classified as functional or organic. The report will highlight the clinical presentation, histopathological features and management plan of laryngeal epidermal inclusion cysts (EICs). Laryngeal EICs are rare. The epidermal and dermoid cysts represent only 0.01% of oral cavity cysts. Their clinical presentation varies from a completely asymptomatic presentation to dysphonia for years. This current report represents a case of a 34-year-old female who presented with 2-year history of dysphonia, which was caused by a unilateral laryngeal EIC.

摘要

发音障碍或声音嘶哑的原因众多,可分为功能性或器质性。本报告将重点介绍喉表皮样囊肿(EIC)的临床表现、组织病理学特征及管理方案。喉表皮样囊肿很罕见。表皮样囊肿和皮样囊肿仅占口腔囊肿的0.01%。其临床表现从完全无症状到数年的发音障碍不等。本报告介绍了一例34岁女性病例,该患者有2年发音障碍病史,由单侧喉表皮样囊肿引起。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c64e/7703371/b80c06dd2c7d/rjaa488f1.jpg

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