Branchiootic syndrome-a clinical case report and review of the literature

被引:3
|
作者
Amer, Imad [1 ]
Falzon, Adam [1 ]
Choudhury, Natasha [1 ]
Ghufoor, Khalid [1 ]
机构
[1] Royal London Hosp, Dept Paediat ENT, London E1 1BB, England
关键词
Branchio-otorenal; Branchial fistula; Second branchial arch anomaly; BOR SYNDROME; HEARING-LOSS; EAR PITS; ANOMALIES;
D O I
10.1016/j.jpedsurg.2012.05.016
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Branchiootoic syndrome is part of the spectrum of brachiootorenal disorders. Brachiootorenal disorder is a rare autosomal dominant condition, characterized by malformations of the outer, middle, and inner ear, which are associated with branchial and renal anomalies. We describe a case of bilateral branchiootoic syndrome and discuss the anatomy of second branchial cleft fistulae and the surgical management of this uncommon condition. We report the case of a 6-year-old girl referred to our department with bilateral intermittently discharging neck swellings. Clinical examination revealed bilateral branchial fistulae and preauricular sinuses, on a background of a positive family history of branchial fistulae. A magnetic resonance imaging scan confirmed the diagnosis of bilateral second branchial cleft fistulae. In view of her symptoms, she underwent bilateral branchial fistula excision and tonsillectomy with an uneventful postoperative recovery. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:1604 / 1606
页数:3
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