Arbell Dan, Orkin Boris, Naveh Yaron, Gur Ilan, Udassin Raphael
Department of Pediatric Surgery, Hadassah University Hospital, Jerusalem 91120, Israel.
J Pediatr Surg. 2006 Jun;41(6):e11-3. doi: 10.1016/j.jpedsurg.2006.02.032.
We present the case of a premature baby who was born with the following conditions: an extensive atresia from the first part of the duodenum to the mid small bowel; malrotation of the distal part, in volvulus and in an "apple peel" configuration; no connection of the bile ducts to the bowel; and presence of a type II choledochal cyst. To our knowledge, this is the first case in which a combination of these anomalies is reported. A brief review of the relevant literature is also presented.
我们报告了一例早产婴儿的病例,该婴儿出生时存在以下情况:十二指肠第一部至小肠中部广泛闭锁;远端肠管旋转不良,呈肠扭转及“苹果皮”样畸形;胆管与肠道无连接;存在II型胆总管囊肿。据我们所知,这是首例报道的合并这些异常情况的病例。本文还对相关文献进行了简要综述。