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儿童先天性第二鳃裂畸形:52例手术病例报告,重点关注特征性CT表现。

Congenital second branchial cleft anomalies in children: A report of 52 surgical cases, with emphasis on characteristic CT findings.

作者信息

Chen Wei, Zhou Yilong, Xu Mengrou, Xu Rong, Wang Qingyu, Xu Hongming, Chen Jiarui, Li Xiaoyan

机构信息

Department of Otolaryngology-Head and Neck Surgery, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.

Department of Pediatric Otorhinolaryngology, Shenzhen Hospital, Southern Medical University, Shenzhen, China.

出版信息

Front Pediatr. 2023 Mar 3;11:1088234. doi: 10.3389/fped.2023.1088234. eCollection 2023.

DOI:10.3389/fped.2023.1088234
PMID:36937970
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10020344/
Abstract

OBJECTIVE

The objectives of this study was to review the clinical features and surgical treatment outcomes of congenital second branchial cleft anomalies (CSBCAs) and to investigate the characteristic computed tomography (CT) findings of CSBCAs.

METHODS

We conducted a retrospective study of 52 children who were referred to Shanghai Children's Hospital from October 2014 to December 2021 diagnosed as CSBCAs.

RESULTS

There were 36 males and 16 females. Of them, 35 patients were presented as having a skin pit at birth or discharge from the skin opening on the lateral neck, and 17 patients presented with an asymptomatic or painful mass. The typical CT features of CSBCAs included isolated and homogeneously hypodense cystic lesions surrounded by a uniformly thin, smooth wall. CSBCAs were generally located at the anteromedial border of the sternocleidomastoid muscle, posterior to the submandibular gland, and lateral to the carotid sheath. All patients were treated surgically and only one case underwent ipsilateral tonsillectomy. After a median follow-up of 30 (range 4-90) months, no recurrence or complications were observed.

CONCLUSIONS

The CSBCAs show some characteristic CT findings, which can help clinicians diagnose and plan surgical strategies. High ligation of the lesions is sufficient for complete excision of CSBCAs.

摘要

目的

本研究旨在回顾先天性第二鳃裂畸形(CSBCAs)的临床特征和手术治疗结果,并探讨CSBCAs的特征性计算机断层扫描(CT)表现。

方法

我们对2014年10月至2021年12月转诊至上海儿童医学中心并被诊断为CSBCAs的52例患儿进行了回顾性研究。

结果

其中男性36例,女性16例。其中,35例患者出生时或出院时表现为颈部外侧皮肤开口处有皮肤凹陷,17例患者表现为无症状或疼痛性肿块。CSBCAs的典型CT特征包括孤立的、均匀低密度的囊性病变,周围有均匀薄而光滑的壁。CSBCAs通常位于胸锁乳突肌的前内侧缘、下颌下腺后方和颈动脉鞘外侧。所有患者均接受了手术治疗,只有1例患者接受了同侧扁桃体切除术。中位随访30(4-90)个月后,未观察到复发或并发症。

结论

CSBCAs表现出一些特征性CT表现,有助于临床医生诊断和制定手术策略。对病变进行高位结扎足以完整切除CSBCAs。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7465/10020344/8802a2d7900e/fped-11-1088234-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7465/10020344/b61a2a0bd029/fped-11-1088234-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7465/10020344/0fa8fa99001d/fped-11-1088234-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7465/10020344/c0e3ab8addf9/fped-11-1088234-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7465/10020344/7654dabf39d4/fped-11-1088234-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7465/10020344/8802a2d7900e/fped-11-1088234-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7465/10020344/b61a2a0bd029/fped-11-1088234-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7465/10020344/0fa8fa99001d/fped-11-1088234-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7465/10020344/c0e3ab8addf9/fped-11-1088234-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7465/10020344/7654dabf39d4/fped-11-1088234-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7465/10020344/8802a2d7900e/fped-11-1088234-g005.jpg

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本文引用的文献

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2
Diagnostic Approach to Congenital Cystic Masses of the Neck from a Clinical and Pathological Perspective.从临床和病理角度看颈部先天性囊性肿物的诊断方法
Dermatopathology (Basel). 2021 Aug 1;8(3):342-358. doi: 10.3390/dermatopathology8030039.
3
Second branchial cleft cyst with snoring during sleep as initial symptom: A case report and literature review.
以睡眠打鼾为首发症状的第二鳃裂囊肿 1 例报告并文献复习
Medicine (Baltimore). 2021 Aug 27;100(34):e27037. doi: 10.1097/MD.0000000000027037.
4
Endoscopic coblation treatment for congenital pyriform sinus fistula in children.儿童先天性梨状窝瘘的内镜电凝治疗。
Medicine (Baltimore). 2021 May 14;100(19):e25942. doi: 10.1097/MD.0000000000025942.
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Endoscopically assisted transoral resection of a Bailey type IV second branchial cleft cyst: A case report.内镜辅助经口切除贝利IV型第二鳃裂囊肿:一例报告
Medicine (Baltimore). 2021 Jan 22;100(3):e24375. doi: 10.1097/MD.0000000000024375.
6
Unusual location of a second branchial cleft cyst presenting in the suprasternal notch.颈前区第二鳃裂囊肿的异常位置。
Head Neck. 2021 Apr;43(4):E27-E29. doi: 10.1002/hed.26629. Epub 2021 Feb 3.
7
Branchial cleft anomalies: hybrid "Branchial Inclusion" theory.鳃裂畸形:杂交“鳃裂包含”理论。
Eur Arch Otorhinolaryngol. 2021 Jul;278(7):2593-2601. doi: 10.1007/s00405-020-06551-1. Epub 2021 Jan 11.
8
Feasibility of same day surgery for pediatric second branchial cleft anomalies.小儿第二鳃裂畸形同日手术的可行性。
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9
Definitive surgical management for second branchial cleft fistula: a case series.第二鳃裂瘘管的确定性手术治疗:病例系列。
J Otolaryngol Head Neck Surg. 2020 Aug 5;49(1):55. doi: 10.1186/s40463-020-00453-2.
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