空肠闭锁的延迟表现。

Q3 Medicine
Charu Sharma, H. Shah, Mukta Waghmare, J. Desale, Pankaj Dwivedi
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引用次数: 3

摘要

I型肠闭锁是婴儿肠梗阻的罕见原因,最常见的部位是十二指肠的第二部分。根据low和Barnard分类,1型闭锁被定义为导致完全(无穿孔的腹壁)或不完全(有中心穿孔的腹壁)肠梗阻的腔内腹壁。空肠是这种网状物的罕见部位。由于中心穿孔导致的不完全阻塞腹膜的诊断通常是困难和具有挑战性的。我们提出两例空肠网与中心穿孔,其中介绍延迟。两者都是通过切除网络来处理的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Delayed presentation of jejunal atresia.
Type I intestinal atresias (webs) are rare causes of gastrointestinal obstruction in infants, the most common site being the second portion of the duodenum. According to the Louw and Barnard classification, type 1 atresia has been defined as an intra-luminal web which results in either complete (web with no perforation) or incomplete (web with central perforation) intestinal obstruction. The jejunum is a rare site of such webs. Diagnosis of an incompletely obstructing web due to central perforation is usually difficult and challenging. We present two cases of jejunal web with a central perforation in which the presentation was delayed. Both were managed by excision of the web.
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来源期刊
Medycyna wieku rozwojowego
Medycyna wieku rozwojowego Medicine-Medicine (all)
CiteScore
0.90
自引率
0.00%
发文量
53
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