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远端结肠闭锁:一例报告。

Distal colonic atresia: a case report.

作者信息

Allert Tom, Schellerer Vera

机构信息

Department of Pediatric Surgery, University Medicine Greifswald, Greifswald, Germany.

出版信息

J Surg Case Rep. 2023 Jun 12;2023(6):rjad335. doi: 10.1093/jscr/rjad335. eCollection 2023 Jun.

Abstract

Colonic atresia (CA) is a rare disease with an incidence range between one of 20 000 and one of 66 000 live births. Most CA are located within the proximal colon; distal CA are even rarer. Because of its rarity, another case shall be described herewith. A 37th week of pregnancy born child was noticed occurring multiple vomiting, a distended abdomen and additional whitish-bloody stool shortly thereafter. In the first operation, a double-barrel stoma was created. After sufficient weight gain and alignment of the stoma ends, a secondary anastomosis was created in the child after 2 months. The diagnosis can be made reliably on the basis of an X-ray and leads to a good outcome with prompt surgical intervention. However, accompanying malformations should always be considered.

摘要

结肠闭锁(CA)是一种罕见疾病,发病率在每20000至66000例活产婴儿中有1例。大多数CA位于近端结肠;远端CA更为罕见。由于其罕见性,现将另一病例予以描述。一名孕37周出生的婴儿出生后不久即出现多次呕吐、腹部膨隆及伴有白色血性粪便。首次手术时行双腔造口术。在患儿体重充分增加且造口两端对齐后,2个月后进行了二期吻合术。根据X线检查可可靠地做出诊断,及时的手术干预可带来良好预后。然而,始终应考虑合并的畸形情况。

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