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1
An Unusual Case of Bilateral First Branchial Cleft Anomaly: A Case Report with Review of Literature.双侧第一鳃裂畸形的罕见病例：病例报告并文献复习
Indian J Otolaryngol Head Neck Surg. 2020 Sep;72(3):381-384. doi: 10.1007/s12070-019-01751-6. Epub 2019 Oct 18.
2
Collaural fistula (Work Type II first branchial cleft anomaly) with prolonged morbidity: A case report.伴有长期发病的耳瘘（工作类型II型第一鳃裂畸形）：病例报告
SAGE Open Med Case Rep. 2021 May 13;9:2050313X211014515. doi: 10.1177/2050313X211014515. eCollection 2021.
3
Complete second branchial cleft anomaly presenting as a fistula and a tonsillar cyst: an interesting congenital anomaly.表现为瘘管和扁桃体囊肿的完全性第二鳃裂畸形：一种有趣的先天性畸形。
Ear Nose Throat J. 2014 Oct-Nov;93(10-11):466-8.
4
Atypical first branchial cleft fistula: A case report.非典型第一鳃裂瘘管：一例报告
Int J Surg Case Rep. 2021 Jan;78:159-161. doi: 10.1016/j.ijscr.2020.12.007. Epub 2020 Dec 5.
5
Importance and Impact of Appropriate Radiology in the Management of Branchial Cleft Anomalies.适当的放射学检查在鳃裂畸形管理中的重要性和影响
Indian J Otolaryngol Head Neck Surg. 2019 Oct;71(Suppl 1):953-959. doi: 10.1007/s12070-019-01634-w. Epub 2019 Mar 23.
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Branchial anomalies in children.儿童鳃裂畸形
Int J Pediatr Otorhinolaryngol. 2011 Aug;75(8):1020-3. doi: 10.1016/j.ijporl.2011.05.008. Epub 2011 Jun 15.
7
First branchial cleft fistula (Work Type 2) with an internal opening to the Eustachian tube: Case report and review of literature.第一鳃裂瘘管（2型）伴咽鼓管内口：病例报告及文献复习
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Branchial Cleft Cyst Associated with Xanthogranulomatous Inflammation - An Unusual Case.鳃裂囊肿伴黄色肉芽肿性炎症——1例罕见病例
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Branchial cleft and pouch anomalies in childhood: a report of 50 surgical cases.儿童鳃裂及咽囊畸形：50例手术病例报告
J Endocrinol Invest. 2016 May;39(5):529-35. doi: 10.1007/s40618-015-0390-8. Epub 2015 Sep 24.
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Nasopharyngeal Branchial Cleft Cyst: A Rare Case Report and Literature Review.鼻咽部鳃裂囊肿：1例罕见病例报告及文献复习
Cureus. 2023 Aug 13;15(8):e43432. doi: 10.7759/cureus.43432. eCollection 2023 Aug.

本文引用的文献

1
[Clinical analysis of branchial cleft cyst (fistula): report of 284 cases].鳃裂囊肿（瘘）的临床分析：附284例报告
Shanghai Kou Qiang Yi Xue. 2008 Oct;17(5):461-4.
2
Fluoroscopic and CT fistulography of the first branchial cleft.第一鳃裂的荧光透视及CT瘘管造影
AJNR Am J Neuroradiol. 2006 Oct;27(9):1817-9.
3
Updating concepts of first branchial cleft defects: a literature review.第一鳃裂畸形概念的更新：文献综述
Int J Pediatr Otorhinolaryngol. 2002 Feb 1;62(2):103-9. doi: 10.1016/s0165-5876(01)00612-7.
4
The double auditory meatus--a rare first branchial cleft anomaly: clinical presentation and treatment.双侧外耳道——一种罕见的第一鳃裂畸形：临床表现与治疗
Am J Otol. 2000 Nov;21(6):837-41.
5
First branchial cleft anomalies: a study of 39 cases and a review of the literature.第一鳃裂畸形：39例病例研究及文献综述
Arch Otolaryngol Head Neck Surg. 1998 Mar;124(3):291-5. doi: 10.1001/archotol.124.3.291.
6
First branchial cleft anomaly.第一鳃裂畸形
Clin Otolaryngol Allied Sci. 1996 Jun;21(3):203-7. doi: 10.1111/j.1365-2273.1996.tb01725.x.
7
First branchial cleft anomalies.第一鳃裂畸形
Laryngoscope. 1980 Mar;90(3):423-36. doi: 10.1002/lary.5540900309.
8
Newer concepts of first branchial cleft defects.第一鳃裂畸形的新概念。
Laryngoscope. 1972 Sep;82(9):1581-93. doi: 10.1288/00005537-197209000-00001.
9
Congenital anomalies of the branchial apparatus: embryology and pathologic anatomy.鳃器先天性异常：胚胎学与病理解剖学
Radiographics. 1992 Sep;12(5):943-60. doi: 10.1148/radiographics.12.5.1529135.
10
Branchial cysts, sinuses and fistulae.鳃裂囊肿、鳃裂窦和鳃裂瘘管。
Clin Otolaryngol Allied Sci. 1978 Feb;3(1):77-92. doi: 10.1111/j.1365-2273.1978.tb00670.x.

双侧第一鳃裂畸形的罕见病例：病例报告并文献复习

An Unusual Case of Bilateral First Branchial Cleft Anomaly: A Case Report with Review of Literature.

作者信息

Dutta Angshuman, Vallur Srujan

机构信息

Command Hospital Air Force, Bangalore, India.

Department of ENT, Command Hospital Air Force, Post Agaram, Old Airport Road, Bangalore, 560007 India.

出版信息

Indian J Otolaryngol Head Neck Surg. 2020 Sep;72(3):381-384. doi: 10.1007/s12070-019-01751-6. Epub 2019 Oct 18.

DOI:10.1007/s12070-019-01751-6
PMID:32728550
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7374669/
Abstract

We report a case of 32 year old male who presented to us with first branchial cleft anomalies on both sides with discharging cutaneous openings on the right side; and cystic swelling on the left side. High index of suspicion is required in such congenital cysts. Surgical exploration and excision is the definitive treatment of a collaural fistula.

摘要

我们报告一例32岁男性患者，其双侧存在第一鳃裂畸形，右侧有皮肤排液开口，左侧有囊性肿物。对于此类先天性囊肿，需要高度怀疑。手术探查和切除是鳃瘘的确定性治疗方法。