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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.

DOI:10.3390/children10071158
PMID:37508655
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10377891/
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/f0fca4c1b893/children-10-01158-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/d289f499ef98/children-10-01158-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/e5751846994a/children-10-01158-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/5b2391265a3a/children-10-01158-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/dce4c39af6d3/children-10-01158-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/8f71f37e4052/children-10-01158-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/264dd4d55848/children-10-01158-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/f0fca4c1b893/children-10-01158-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/d289f499ef98/children-10-01158-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/e5751846994a/children-10-01158-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/5b2391265a3a/children-10-01158-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/dce4c39af6d3/children-10-01158-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/8f71f37e4052/children-10-01158-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/264dd4d55848/children-10-01158-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8864/10377891/f0fca4c1b893/children-10-01158-g007.jpg

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本文引用的文献

1
Congenital first branchial cleft anomalies in children: a study of 100 surgical cases and a review of the literature.儿童先天性第一鳃裂畸形:100例手术病例研究及文献综述
Eur Arch Otorhinolaryngol. 2023 Jan;280(1):425-433. doi: 10.1007/s00405-022-07607-0. Epub 2022 Aug 30.
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Analysis of the Clinical Features and Surgical Outcomes of First Branchial Cleft Anomalies.第一鳃裂畸形的临床特征及手术治疗效果分析。
Laryngoscope. 2022 May;132(5):1008-1014. doi: 10.1002/lary.29896. Epub 2021 Oct 7.
3
Clinical analysis of first branchial cleft anomalies in children.
儿童第一鳃裂畸形的临床分析
Pediatr Investig. 2018 Oct 17;2(3):149-153. doi: 10.1002/ped4.12051. eCollection 2018 Sep.
4
Clinical Analysis of Type II First Branchial Cleft Anomalies in Children.儿童 II 型第一鳃裂畸形的临床分析。
Laryngoscope. 2021 Apr;131(4):916-920. doi: 10.1002/lary.29049. Epub 2020 Aug 26.
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First branchial cleft anomalies in children: Experience with 30 cases.儿童第一鳃裂畸形:30例经验
Exp Ther Med. 2017 Jul;14(1):333-337. doi: 10.3892/etm.2017.4511. Epub 2017 May 24.
6
The treatment for the first branchial cleft anomalies in children.儿童第一鳃裂畸形的治疗
Eur Arch Otorhinolaryngol. 2017 Sep;274(9):3465-3470. doi: 10.1007/s00405-017-4648-y. Epub 2017 Jun 20.
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First branchial cleft anomalies: otologic manifestations and treatment outcomes.第一鳃裂畸形:耳科表现及治疗结果
Otolaryngol Head Neck Surg. 2015 Mar;152(3):506-12. doi: 10.1177/0194599814562773. Epub 2014 Dec 18.
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First branchial cleft anomalies: presentation, variability and safe surgical management.第一鳃裂畸形:表现、变异性及安全手术治疗。
Eur Arch Otorhinolaryngol. 2013 May;270(6):1917-25. doi: 10.1007/s00405-012-2287-x. Epub 2012 Nov 29.
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First branchial arch abnormality: diagnostic dilemma and excision with facial nerve preservation.第一鳃弓异常:诊断困境与面神经保留切除术
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First branchial cleft fistula presenting with internal opening on the Eustachian tube: Illustrated cases and literature review.表现为咽鼓管内口开口的第一鳃裂瘘管:病例展示与文献综述
Int J Pediatr Otorhinolaryngol. 2012 May;76(5):642-5. doi: 10.1016/j.ijporl.2012.01.028. Epub 2012 Feb 14.