Title of article
Midgut volvulus in an adult with congenital malrotation
Author/Authors
Sheng-Der Hsu، نويسنده , , Jyh-Cherng Yu، نويسنده , , Shao-Jiun Chou، نويسنده , , Huan-Fa Hsieh، نويسنده , , Tsun-Hou Chang، نويسنده , , Yao-Chi Liu، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2008
Pages
3
From page
705
To page
707
Abstract
Congenital midgut malrotation, a rare anatomic anomaly that can lead to duodenal or small-bowel obstruction, rarely is observed beyond the first year of life. Symptomatic patients present with either acute bowel obstruction and intestinal ischemia with a midgut or cecal volvulus or with chronic vague abdominal pain. Chronic symptoms often can make the diagnosis difficult. By using several modalities such as barium studies, computerized tomography, angiography, and emergency laparotomy, we diagnosed midgut volvulus and partial intestinal obstruction, which occur rarely in an adult with congenital midgut malrotation.
Keywords
Volvulus , midgut
Journal title
The American Journal of Surgery
Serial Year
2008
Journal title
The American Journal of Surgery
Record number
619065
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