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空肠闭锁的延迟表现。

Delayed presentation of jejunal atresia.

作者信息

Sharma Charu, Shah Hemanshi, Waghmare Mukta, Desale Jayesh, Dwivedi Pankaj

机构信息

Dept of Paediatric Surgery, TNMC & BYLNair Hospital, Mumbai Central, Mumbai, Maharashtra. India. Pin: 400008.

出版信息

Dev Period Med. 2017;21(2):95-97. doi: 10.34763/devperiodmed.20172102.9597.

Abstract

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.

摘要

I型肠闭锁(隔膜)是婴儿胃肠道梗阻的罕见原因,最常见的部位是十二指肠第二部。根据Louw和Barnard分类,1型闭锁被定义为腔内隔膜,可导致完全性(无穿孔的隔膜)或不完全性(中央穿孔的隔膜)肠梗阻。空肠是此类隔膜的罕见部位。因中央穿孔导致的不完全梗阻性隔膜的诊断通常困难且具有挑战性。我们报告两例中央穿孔的空肠隔膜病例,其临床表现出现延迟。两例均通过隔膜切除术进行治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc19/8522967/9b6044bfa78c/jmotherandchild-21-095-g001.jpg

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