Oudshoorn J H, Heij H A
Department of Paediatric Surgery EKZ/AMC, Amsterdam, The Netherlands.
Eur J Pediatr. 1996 Apr;155(4):338-40. doi: 10.1007/BF02002724.
Two cases of caecal duplication are presented, one in a neonate and one in an infant. The diagnosis was made at laparotomy, which had been undertaken for the presumptive diagnosis of intestinal atresia and torsion of an ovarian cyst respectively. Also the literature on alimentary tract duplications is reviewed, referring to the incidence, presenting symptoms, and location of the duplication, in particular that of the caecum.
本文报告两例盲肠重复畸形病例,一例为新生儿,另一例为婴儿。诊断是在剖腹手术时做出的,这两例手术最初分别是因疑似肠道闭锁和卵巢囊肿扭转而进行的。同时,本文还回顾了消化道重复畸形的相关文献,涉及重复畸形的发病率、临床表现及位置,尤其是盲肠重复畸形的情况。