Madana J, Yolmo D, Gopalakrishnan S, Saxena S K
Department of Otorhinolaryngology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India.
J Laryngol Otol. 2010 Sep;124(9):1025-9. doi: 10.1017/S0022215110000034. Epub 2010 Feb 16.
We report an extremely rare case of a complete congenital third branchial arch fistula in a nine-year-old boy.
A case report and a review of the English literature concerning third branchial arch fistula of congenital origin are presented.
A nine-year-old boy presented with a history of a small opening in the middle third of the anterior neck since birth, with recurrent surrounding swelling. There was no history of surgical drainage or spontaneous rupture. Computed tomography with contrast injection into the external cervical opening revealed a patent tract from the neck skin to the base of the pyriform sinus. Complete excision of the tract up to the pyriform sinus with left hemithyroidectomy was performed. Follow up at 22 months showed no recurrence.
To our knowledge, this case represents a very rare occurrence of the congenital variety of complete third branchial arch fistula at an unusual site. This case indicates that third branchial arch fistula can be complete, and may present in the anterior neck, an unusual site. In such cases, computed tomography fistulography and injection of dye into the pyriform sinus enables intra-operative delineation of the tract.
我们报告一例极为罕见的9岁男孩先天性完全性第三鳃裂瘘管病例。
本文呈现一例病例报告,并对先天性第三鳃裂瘘管的英文文献进行综述。
一名9岁男孩自出生以来,在前颈部中三分之一处有一个小开口,并伴有周围反复肿胀。无手术引流或自发破裂史。经颈外开口注入造影剂的计算机断层扫描显示,存在一条从颈部皮肤至梨状窦底部的瘘管。对瘘管直至梨状窦进行了完整切除,并切除了左侧甲状腺叶。22个月的随访显示无复发。
据我们所知,该病例代表了先天性完全性第三鳃裂瘘管在不寻常部位的极为罕见的情况。该病例表明,第三鳃裂瘘管可以是完全性的,且可能出现在前颈部这一不寻常部位。在此类病例中,计算机断层扫描瘘管造影及向梨状窦注入染料可在术中明确瘘管情况。