Benhamou G, Armstrong O, Lanz M, Bocquet L
J Chir (Paris). 1984 Jun-Jul;121(6-7):451-6.
Duodenal duplication is a rare congenital malformation and it is quite exceptional for it to be discovered in adult life. Three recently observed cases are discussed and used as a basis for reviewing diagnostic and surgical therapeutic problems. Pathology provides confirmation of diagnosis.
十二指肠重复畸形是一种罕见的先天性畸形，在成人期发现极为罕见。本文讨论了最近观察到的三例病例，并以此为基础回顾诊断和手术治疗问题。病理学可确诊。
