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极低出生体重儿肠道肌肉节段性缺如并伴有回肠蹼:病例报告

Segmental absence of intestinal muscle with ileal web in an extremely low birth weight infant: case report.

作者信息

Buyuktiryaki Mehmet, Kanmaz Hayriye G, Okur Nilüfer, Ates Ufuk, Sirvan Ali L, Uras Nurdan

机构信息

Division of Neonatology, Dr. Zekai Tahir Burak Kadin Sagligi Egitim ve Arastirma Hastanesi, Ankara, 06230, Turkey.

Division of Pediatric Surgery, Dr. Zekai Tahir Burak Kadin Sagligi Egitim ve Arastirma Hastanesi, Ankara, 06230, Turkey.

出版信息

Arch Argent Pediatr. 2016 Apr;114(2):e108-10. doi: 10.5546/aap.2016.eng.e108. Epub 2016 Apr 1.

Abstract

Spontaneous intestinal perforations are localized perforations without the typical clinical, radiological, and histopathological features of necrotizing enterocolitis. Spontaneous intestinal perforation is a recently defined clinical entity. The best-known risk factor is prematurity. It is seen 2-3% in very low birthweight infants and 5 % of extremely low birthweight infants. Herein we report an extremely low birthweight infant with spontaneous intestinal perforation, segmental absence of intestinal muscle and an ileal web as an underlying cause. We aimed to draw attention to the segmental absence of intestinal muscle which is rare but increasingly reported cause of spontaneous intestinal perforation and the importance of histopathologic examination of surgical specimens.

摘要

自发性肠穿孔是局限性穿孔,不具有坏死性小肠结肠炎的典型临床、放射学和组织病理学特征。自发性肠穿孔是最近定义的一种临床病症。最知名的危险因素是早产。在极低出生体重儿中发生率为2% - 3%,在超低出生体重儿中为5%。在此,我们报告一例超低出生体重儿发生自发性肠穿孔,其潜在病因是肠肌节段性缺失和回肠蹼。我们旨在提醒人们注意肠肌节段性缺失这种虽罕见但报告日益增多的自发性肠穿孔病因,以及手术标本组织病理学检查的重要性。

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