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一名患有内脏异位综合征的儿童发生自发性胃穿孔。

Spontaneous gastric perforation in a child with heterotaxy syndrome.

作者信息

Schinasi Dana Aronson, Ellison Angela M

机构信息

Department of Emergency Medicine, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

出版信息

Pediatr Emerg Care. 2010 Dec;26(12):925-7. doi: 10.1097/PEC.0b013e3181fe9175.

Abstract

Gastric perforation is a potentially fatal condition that is rare in infants and children. Most case reports in the pediatric population are of neonates or in patients with various associated risk factors including prematurity, ischemia, trauma, or ulcers. Heterotaxy syndrome is characterized by abnormal symmetry and malposition of the thoracoabdominal organs and vessels. Spontaneous gastric perforation has not previously been reported in a child with heterotaxy syndrome. We present a case of a child with heterotaxy syndrome who presented with spontaneous gastric perforation. We review the signs and the symptoms, radiographic clues, and diagnostic considerations of gastric perforation.

摘要

胃穿孔是一种潜在的致命病症,在婴儿和儿童中较为罕见。儿科人群中的大多数病例报告是关于新生儿或伴有各种相关风险因素的患者,这些因素包括早产、缺血、创伤或溃疡。内脏异位综合征的特征是胸腹器官和血管的对称性异常和位置异常。此前尚未有关于内脏异位综合征患儿发生自发性胃穿孔的报道。我们报告一例患有内脏异位综合征的患儿出现自发性胃穿孔的病例。我们回顾了胃穿孔的体征和症状、影像学线索及诊断要点。

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