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儿童第一鳃裂畸形:一种预防外耳道狭窄的创新手术技术

First Brachial Cleft Anomalies in Children: An Innovative Surgical Technique Preventing External Auditory Canal Stenosis.

作者信息

Kotowski Michal, Szydlowski Jaroslaw

机构信息

Department of Pediatric Otolaryngology, Poznan University of Medical Sciences, 60-572 Poznan, Poland.

出版信息

Children (Basel). 2023 Jul 1;10(7):1158. doi: 10.3390/children10071158.

Abstract

First branchial cleft anomalies (FBCAs) are rare congenital malformations that require complete surgical removal. A stenosis of the external auditory canal (EAC) may be the consequence of the disease and its treatment. The aim of this study is to present the details and results of an innovative surgical technique using part of the abnormality for reconstruction purposes. This study covered 28 surgically treated children with FCBA between 2014 and 2021. The analysis included the clinical manifestation form of the abnormality, presence of the EAC deformity, histopathological results, complications, and distant results. On the basis of Work's classification system, 15 pediatric patients with type II FBCA and 13 children with type I FBCA were included in the further study. One child with type II FBCA and two with type I FBCA had a normal EAC. The preoperative appearance of the EAC was classified into three main types, each potentially accompanied by a skin ostium of the sinus/fistula in the EAC. Reconstruction with our technique was performed in 14 children (1 with type I FBCA and 13 with type II FBCA). Wound healing was uncomplicated in all cases. No recurrences were observed. This innovative surgical technique of the subtotal resection of FBCAs with simultaneous reconstruction is safe and prevents postoperative EAC stenosis. Despite the deliberate use of part of the abnormality wall for reconstructive purposes, it remained free of recurrences.

摘要

第一鳃裂畸形(FBCAs)是罕见的先天性畸形,需要进行完整的手术切除。外耳道(EAC)狭窄可能是该疾病及其治疗的后果。本研究的目的是介绍一种利用部分异常进行重建的创新手术技术的细节和结果。本研究涵盖了2014年至2021年间28例接受手术治疗的FBCA患儿。分析内容包括异常的临床表现形式、EAC畸形的存在情况、组织病理学结果、并发症和远期结果。根据Work分类系统,进一步研究纳入了15例II型FBCA患儿和13例I型FBCA患儿。1例II型FBCA患儿和2例I型FBCA患儿的EAC正常。EAC的术前外观分为三种主要类型,每种类型可能伴有EAC内窦道/瘘管的皮肤开口。14例患儿(1例I型FBCA和13例II型FBCA)采用我们的技术进行了重建。所有病例伤口愈合均无并发症。未观察到复发情况。这种同时进行FBCAs次全切除并重建的创新手术技术是安全的,可防止术后EAC狭窄。尽管故意将部分异常壁用于重建目的,但仍未出现复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/d289f499ef98/children-10-01158-g001.jpg

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