Ford G R, Balakrishnan A, Evans J N, Bailey C M
ENT Department, Cambridge Military Hospital, Aldershot, Hants.
J Laryngol Otol. 1992 Feb;106(2):137-43. doi: 10.1017/s0022215100118900.
We present a retrospective study of 106 patients with branchial cleft and pouch anomalies who presented to the Hospital for Sick Children between 1948 and 1990. The relevant embryology of the branchial apparatus is summarized and a theoretical description of individual anomalies given. Second branchial cleft sinuses were the most common anomalies, and the majority were managed simply, with adequate excision and a low recurrence rate. Five cases of first branchial cleft anomalies are presented, emphasizing the delay in diagnosis, the need for complete excision to prevent recurrence, and for a parotidectomy incision to protect the facial nerve from damage. The two third branchial pouch anomalies presented with a cystic neck swelling, one with recurrent infection and discharge, and the other with stridor. In both, the diagnosis was made at operation. The single fourth branchial pouch cyst was an unexpected finding in a patient with stridor.
我们对1948年至1990年间在病童医院就诊的106例鳃裂和鳃囊异常患者进行了一项回顾性研究。总结了鳃器的相关胚胎学,并对个体异常进行了理论描述。第二鳃裂窦是最常见的异常,大多数通过充分切除得到简单处理,复发率较低。本文介绍了5例第一鳃裂异常病例,强调了诊断延迟、为防止复发进行完全切除的必要性以及采用腮腺切除术切口以保护面神经免受损伤。2例第三鳃囊异常表现为颈部囊性肿胀,1例伴有反复感染和分泌物排出,另1例伴有喘鸣。两者均在手术时确诊。这例单发的第四鳃囊囊肿是在一名喘鸣患者中意外发现的。