From a branchial fistula to a branchiootorenal syndrome: a case report and review of the literature

被引:8
|
作者
Senel, Emrah [1 ]
Kocak, Hatice [2 ]
Akbiyik, Fatih [1 ]
Saylam, Guleser [3 ]
Gulleroglu, Basak Nadide [4 ]
Senel, Saliha [5 ]
机构
[1] Diskapi Childrens Hosp, Dept Pediat Surg, TR-06110 Ankara, Turkey
[2] Diskapi Childrens Hosp, Dept Genet, TR-06110 Ankara, Turkey
[3] Diskapi Hosp, Dept Pediat Ear Nose Throat, TR-06110 Ankara, Turkey
[4] Diskapi Childrens Hosp, Dept Pediat Radiol, TR-06110 Ankara, Turkey
[5] Dr Sami Ulus Childrens Hosp, Dept Pediat, TR-06110 Ankara, Turkey
关键词
Branchiootorenal syndrome; Branchial anomalies; Hearing impairment; Preauricular pit; OTO-RENAL-SYNDROME; BOR SYNDROME; HEARING-LOSS; EYA1; GENE; MUTATION; FAMILY;
D O I
10.1016/j.jpedsurg.2008.10.034
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Branchial abnormalities constitute 32% to 45% of all neck pathologies in children. They may be a part of branchiootorenal (BOR) syndrome, which is characterized by branchial arch anomalies, preauricular pits, hearing impairment, and renal malformations. Typically, the management of a branchial fistula does not necessarily require an extensive diagnostic workup. However, in patients with a branchial fistula associated with external ear anomalies on physical examination and/or a history of hearing loss and a similar history and findings in other family members, an additional workup should be performed to eliminate the possibility of BOR syndrome. The aim of this report is to make pediatric surgeons aware of the BOR syndrome in patients presenting with branchial arch anomalies. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:623 / 625
页数:3
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