Easa Sabry Habashy, Selim Ahmed Nabil, Ali Elshahat Gaballah
Department of Otorhinolaryngology, Faculty of Medicine, Al-Azhar University, Assiut, MD Egypt.
Department of Otorhinolaryngology, Faculty of Medicine, Al-Azhar University, Assiut, Egypt.
Indian J Otolaryngol Head Neck Surg. 2024 Aug;76(4):3497-3500. doi: 10.1007/s12070-024-04583-1. Epub 2024 Mar 13.
Branchial arch anomalies are considered congenital defects that can occur during fetal development. They may present as cysts, sinuses, or fistulae. Anomalies of the second branchial arch are the most common. The existence of bilateral complete fistulae is exceptionally rare. In this case report, a 5-year-old boy presented with recurrent episodes of bilateral neck swelling and watery discharge from openings on the anterolateral sides of his neck since birth. He was diagnosed with bilateral branchial fistulae after confirmation via a contrast-enhanced CT scan. Surgery was performed to entirely excise the fistula tracts bilaterally. Additionally, a bilateral tonsillectomy was performed to help prevent recurrence.
鳃弓异常被认为是胎儿发育过程中可能出现的先天性缺陷。它们可能表现为囊肿、窦道或瘘管。第二鳃弓异常最为常见。双侧完全瘘管的情况极为罕见。在本病例报告中,一名5岁男孩自出生以来双侧颈部反复肿胀,颈部前外侧开口处有水样分泌物。经增强CT扫描确诊后,他被诊断为双侧鳃瘘。手术双侧完全切除瘘管。此外,还进行了双侧扁桃体切除术以帮助预防复发。