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鳃源性梨状窝瘘继发颈部感染。

Cervical infection secondary to pyriform sinus fistula of branchial origin.

作者信息

Madana J, Yolmo Deeke, Gopalakrishnan S, Saxena Sunil Kumar

机构信息

Department of Otorhinolaryngology, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Pondicherry, India.

出版信息

Congenit Anom (Kyoto). 2009 Dec;49(4):276-8. doi: 10.1111/j.1741-4520.2009.00249.x.

Abstract

Complete third branchial arch anomalies are rare and have been described only in case reports, affecting mainly children and typically presenting as a cervical inflammatory process. Anomalies of the third and fourth branchial apparatus, though rare, usually present as sinuses/incomplete fistulas of pyriform sinus or recurrent suppurative thyroiditis. A 6-year-old girl presented with a small opening on the left side of her anterior neck, which had been present since birth and was associated with recurrent infection. She had no history of incision and drainage of swelling. Computed tomography with contrast injection into the cervical opening revealed a fistulous tract extending from the cervical neck skin to the pyriform fossa. Complete excision of the fistulous tract and left hemithyroidectomy were performed. There was no recurrence at 22 months of follow-up.

摘要

完全性第三鳃弓异常较为罕见,仅在病例报告中有所描述,主要影响儿童,通常表现为颈部炎性病变。第三和第四鳃器异常虽罕见,但通常表现为梨状窝窦道/不完全瘘管或复发性化脓性甲状腺炎。一名6岁女孩,其颈前部左侧自出生就有一个小开口,并伴有反复感染。她没有肿胀切开引流史。向颈部开口处注射造影剂后的计算机断层扫描显示,有一条瘘管从颈部皮肤延伸至梨状窝。遂行瘘管完全切除术及左侧甲状腺半切除术。随访22个月无复发。

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