Vefa KINIŞ, Cüneyt KUCUR, Yusuf EREN, Ali Okan GÜRSEL

Bilateral branchial cleft anomaly type two and type three seen together

Yaşamın ikinci haftasından itibaren oluşmaya başlayan herbir brankiyal yapı, baş ve boyun bölgesinde farklı yapıları oluşturmaktadır. Brankiyal yarık anomalileri zamanla kapanması gereken bu yapıların kapanmaması sonucu gelişmektedir. Her yaş grubunda görülebilmekle beraber sıklıkla çocukluk döneminde görülmektedir. Brankiyal yarık anomalileri sık görülmekle birlikte bilateral olarak bildirilen vakalar oldukça nadirdir. Biz 14 yaşında bilateral brankiyal yarık anomalisi teşhisi konulan ve bu nedenle opere edilen erkek hastayı sunduk.

Tip iki ve tip üçün birlikte görüldüğü bilateral brankial yarık anomalisi

Branchial apparatus begins to develop at about second week of gestation and each complex will transform into different structures in the head and neck. Branchial cleft anomalies develop due to defect in the closure of these structures by time. Branchial cleft anomalies may be diagnosed at any age but most of them are seen in pediatric population. Although, branchial cleft anomalies are frequently seen, bilateral cases, which have been reported are very rare. We present a 14 years old boy who was diagnosed and operated due to bilateral branchial cleft anomaly. J Clin Exp Invest 2012; 3(1): 99-101

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