Dias Andre Roncon, Lopes Roberto Iglesias, do Couto Rodrigo Carmo, Bonafe Wanderley Wesley, D'Angelo Leticia, Salvestro Maria Luiza
Department of General Surgery, Hospital Universitario, University of Sao Paulo, Sao Paulo, Brazil.
J Surg Educ. 2007 Jan-Feb;64(1):51-3. doi: 10.1016/j.cursur.2006.09.003.
Intestinal duplications are rare congenital lesions that can develop anywhere along the alimentary tract. Symptoms usually appear during the first year of life and are varied. Diagnosis is difficult to achieve, and surgery is required for treatment. Here the case of a 6-month-old male with history of recurrent intussusception is reported. Surgery was indicated, and an ileal duplication was found. Intestinal duplication is discussed based on its epidemiology, clinical presentation, diagnosis, and treatment.
肠重复畸形是罕见的先天性病变，可发生于消化道的任何部位。症状通常在出生后第一年内出现，且多种多样。诊断困难，治疗需要手术。本文报道了一名6个月大、有复发性肠套叠病史的男性病例。该病例有手术指征，术中发现了一段回肠重复畸形。本文基于肠重复畸形的流行病学、临床表现、诊断及治疗进行了讨论。
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