Branchial cleft fistula to branchio-oto-renal syndrome: A case report and literature review

被引:11
|
作者
Li, Hong-Xia [1 ]
Zhou, Peng [2 ]
Tong, Min [3 ]
Zheng, Yan [2 ]
机构
[1] Sichuan Univ, West China Guangan Hosp, Otorhinolaryngol Head & Neck Surg, Guangan, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Otorhinolaryngol Head & Neck Surg, Chengdu 610000, Sichuan, Peoples R China
[3] Leshan Peoples Hosp, Otorhinolaryngol Head & Neck Surg, Leshan, Sichuan, Peoples R China
关键词
Branchial cleft abnormality; branchio-oto-renal syndrome; hearing loss; case report; fistulectomy; tympanoplasty; congenital neck malformation; pediatric; BOR SYNDROME; HEARING-LOSS; ANOMALIES;
D O I
10.1177/0300060520926363
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Branchial cleft abnormality is a common congenital neck malformation in children, which is caused by the abnormal development of the gill sac or gill groove. It is mainly manifested as a cyst in the sinus tract and fistula in the neck, as well as branchio-oto-renal syndrome (BORS). As a rare autosomal dominant genetic disease, the typical manifestations of BORS are hearing loss, abnormal branchial cleft development and renal dysplasia. In this paper, a patient was admitted to the hospital for bilateral branchial cleft fistulas combined with bilateral anterior auricular fistulas, auricular appendix, auricle dysplasia, external auditory canal stenosis, and hearing loss. The patient was diagnosed with BORS, and underwent fistulectomy of the neck and anterior ear, external auditory canal formation, and tympanoplasty. The aim of this report is to strengthen clinicians' understanding of BORS and reduce the rate of clinical missed diagnosis through our case report and literature review.
引用
收藏
页数:7
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