一名成年男性的症状性尾肠重复囊肿（直肠后囊性错构瘤）病例。
A case of symptomatic tailgut duplication cyst(retro-rectal cystic hamartoma) in an adult male.
作者信息
Sarkar Koushik, Kabiraj Pranay, Deoghuria Debasis, Bardhan Jayati
机构信息
Department of Radiodiagnosis, Bankura Sammilani MedicalCollege, Bankura, West Bengal.
出版信息
BJR Case Rep. 2017 Jun 22;3(4):20150422. doi: 10.1259/bjrcr.20150422. eCollection 2017.
Tailgut duplication cyst (retro-rectal cystic hamartoma) is a rare congenital developmental lesion arising from post-natal primitive gut remnants. Tailgut cysts are found more commonly in middle-aged females. It may be asymptomatic or symptomatic in complicated cases. Major differentials include epidermoid cyst, dermoid cyst and anterior meningocele. Unfortunately no radiological sign can specifically diagnose it and surgical resection and histopathology remain the cornerstone for diagnosis. Here we present a case of symptomatic tailgut duplication cyst in an adult male.
尾肠重复囊肿（直肠后囊性错构瘤）是一种罕见的先天性发育性病变，由出生后原始肠管残余物引起。尾肠囊肿在中年女性中更为常见。它可能无症状，也可能在复杂病例中有症状。主要鉴别诊断包括表皮样囊肿、皮样囊肿和前脑膨出。不幸的是，没有影像学征象能特异性诊断该病，手术切除和组织病理学检查仍是诊断的基石。在此，我们报告一例成年男性有症状的尾肠重复囊肿病例。
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