Stringer M D, Brereton R J, Drake D P, Wright V M
Queen Elizabeth Hospital for Children, London, England.
J Pediatr Surg. 1992 May;27(5):576-80. doi: 10.1016/0022-3468(92)90450-l.
Four neonates with double duodenal atresia/stenosis are described. Preoperative plain radiographs in two patients demonstrated atypical appearances suggestive of complex pathology. Cystic dilatation of the second part of the duodenum was observed at laparotomy in two patients and in one of these the "cyst" was palpable preoperatively, causing diagnostic confusion. All four patients underwent successful surgery but one infant with Down's syndrome subsequently died of congenital heart disease.
本文描述了4例患有双重十二指肠闭锁/狭窄的新生儿。两名患者的术前X线平片显示出非典型表现，提示存在复杂病变。两名患者在剖腹手术中观察到十二指肠第二部的囊性扩张，其中一名患者术前可触及“囊肿”，造成诊断混淆。所有4例患者均成功接受了手术，但一名患有唐氏综合征的婴儿随后死于先天性心脏病。
