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罕见的新生儿毛霉病播散病例,表现为坏死性小肠结肠炎伴坏死性筋膜炎。

Rare case of disseminated neonatal zygomycosis mimicking necrotizing enterocolitis with necrotizing fasciitis.

机构信息

Department of Hepato-Billiary-Pancreatic and Pediatric Surgery, Saitama Medical Center, Saitama Medical University, Kamoda 1981, Kawagoe, Saitama, 3508550, Japan.

出版信息

J Pediatr Surg. 2011 Oct;46(10):E29-32. doi: 10.1016/j.jpedsurg.2011.06.018.

Abstract

A set of monochorionic male twins presented with intestinal perforation. The smaller twin was diagnosed with necrotizing enterocolitis followed by sepsis, disseminated intravascular coagulation, and necrotizing fasciitis of the abdominal wall. The infant died on the fourth day after surgery, 16 days after birth. Surgical specimens and autopsy revealed a disseminated zygomycotic infection. Gastrointestinal zygomycosis followed by necrotizing fasciitis in premature infants is a rare condition and mimics necrotizing enterocolitis clinically. Necrotizing fasciitis after gastrointestinal zygomycosis in premature infants is considered a poor prognostic sign. Gastrointestinal zygomycosis should be considered in the differential diagnosis of necrotizing enterocolitis.

摘要

一组单绒毛膜男性双胞胎出现肠穿孔。较小的双胞胎被诊断患有坏死性小肠结肠炎,随后发生脓毒症、弥散性血管内凝血和腹壁坏死性筋膜炎。婴儿在手术后第四天,出生后第 16 天死亡。手术标本和尸检显示出弥漫性接合菌感染。胃肠道接合菌病随后在早产儿中发生坏死性筋膜炎是一种罕见的情况,临床上类似于坏死性小肠结肠炎。早产儿胃肠道接合菌病后发生坏死性筋膜炎被认为是预后不良的标志。在鉴别诊断坏死性小肠结肠炎时应考虑胃肠道接合菌病。

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