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内镜辅助下经耳蜗下途径切除大型先天性鼓室下胆脂瘤:一例报告

Endoscopic Assisted Infracochlear Approach for Excision of a Large Congenital Hypotympanic Cholesteatoma: A Case Report.

作者信息

Kumar Sudesh, Sharma Shivbrat, Chauhan Narvir

机构信息

Department of Otolaryngology, Head, and Neck Surgery, Dr. Rajendra Prashad Medical College, Himachal Pradesh, India.

Radiodiagnosis, Dr. Rajendra Prashad Medical College, Himachal Pradesh, India.

出版信息

Oman Med J. 2023 Jul 31;38(4):e537. doi: 10.5001/omj.2023.37. eCollection 2023 Jul.

Abstract

Congenital cholesteatoma is a rare lesion resulting from failed involution of epidermoid rest cells, which take part in the formation of the mucosa of the middle ear cleft during embryonic development. We report the first case report of a large congenital hypotympanic cholesteatoma with extension to the jugular foramen and carotid canal, in a 13-year-old girl, which was excised successfully by endoscopic-assisted hypotympanotomy infra-cochlear approach.

摘要

先天性胆脂瘤是一种罕见的病变,由表皮样残余细胞退化失败所致,这些细胞在胚胎发育过程中参与中耳裂黏膜的形成。我们报告了首例13岁女孩的大型先天性下鼓室胆脂瘤,其病变延伸至颈静脉孔和颈动脉管,通过内镜辅助下鼓室切开术经耳蜗下入路成功切除。

相似文献

本文引用的文献

1
Transcanal Endoscopic Ear Surgery for Congenital Cholesteatoma.经耳道内镜下先天性胆脂瘤耳手术
Clin Exp Otorhinolaryngol. 2018 Dec;11(4):233-241. doi: 10.21053/ceo.2018.00122. Epub 2018 Jun 27.
7
The utility of diffusion-weighted imaging for cholesteatoma evaluation.扩散加权成像在胆脂瘤评估中的应用。
AJNR Am J Neuroradiol. 2011 Mar;32(3):430-6. doi: 10.3174/ajnr.A2129. Epub 2010 May 20.
8
Congenital cholesteatoma in a case of congenital aural atresia.先天性外耳道闭锁病例中的先天性胆脂瘤。
Otol Neurotol. 2007 Aug;28(5):725; author reply 725-6. doi: 10.1097/01.mao.0000281799.06079.35.
9
Non-classical presentation of congenital cholesteatoma.先天性胆脂瘤的非典型表现。
Ann R Coll Surg Engl. 2007 Mar;89(2):W6-8. doi: 10.1308/147870807X160425.
10
Congenital cholesteatoma clinical features and surgical results.先天性胆脂瘤的临床特征及手术结果。
Am J Otolaryngol. 2006 Sep-Oct;27(5):299-305. doi: 10.1016/j.amjoto.2005.11.016.

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