Congenital short-gut syndrome

被引：0
|
作者：
Gauravi Sabharwal
Peter J. Strouse
Saleem Islam
Najeeb Zoubi
机构：
[1] C.S. Mott Children’s Hospital,Section of Pediatric Radiology
[2] Room F3503,Division of Pediatric Surgery
[3] Department of Radiology,Division of Pediatric Gastroenterology
[4] University of Michigan Health System,undefined
[5] C.S. Mott Children’s Hospital,undefined
[6] Department of Surgery,undefined
[7] University of Michigan Health System,undefined
[8] C.S. Mott Children’s Hospital,undefined
[9] Department of Pediatrics,undefined
[10] University of Michigan Health System,undefined
来源：
Pediatric Radiology | 2004年 / 34卷
关键词：
Barium enema; Congenital short-gut syndrome; Infant; Malrotation; Upper gastrointestinal examination;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
A case of congenital short gut is reported in a 4-month-old boy presenting with failure to thrive. Upper gastrointestinal examination (UGI) with small bowel follow-through (SBFT) demonstrated dilation of the duodenum and jejunum, with rapid transit to rectum. On barium enema (BE), rapid transit of barium was noted to the dilated proximal small bowel seen on UGI/SBFT. Neither study delineated the ileocecal region, and the overall length of bowel appeared short. The diagnosis of congenital short gut was confirmed at surgery. Congenital short-gut syndrome is a rare entity. The diagnosis can be suggested by imaging, but is usually confirmed operatively.
引用
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页码：424 / 427
页数：3
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