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一名两岁儿童的胃肠道毛霉菌病:一个临床和放射学谜团。

Gastrointestinal Mucormycosis in a two-year-old child: A clinical and radiological enigma.

作者信息

Nidhi Mahajan, Sadia Khanam, Khatri Arti, Arnab Ghosh, Khan Niyaz Ahmed

机构信息

Department of Pathology, Chacha Nehru Bal Chikitsalaya, Geeta Colony, Delhi, 110031, India.

Department of Microbiology, Chacha Nehru Bal Chikitsalaya, Geeta Colony, Delhi, 110031, India.

出版信息

Med Mycol Case Rep. 2019 Aug 1;26:5-9. doi: 10.1016/j.mmcr.2019.07.007. eCollection 2019 Dec.

Abstract

Mucormycosis is a rare, fatal angioinvasive infection occurring in immunocompromised individuals. Gastrointestinal mucormycosis is rare variety with high mortality rate. We present a case of GI mucormycosis in a 2-year-old male child who presented with abdominal mass with no underlying risk factors. The aim of this case report is to emphasize on its etiopathogenesis and keeping mucormycosis high in the differential diagnosis in a child presenting with abdominal mass.

摘要

毛霉菌病是一种发生在免疫功能低下个体中的罕见的、致命的血管侵袭性感染。胃肠道毛霉菌病是一种罕见的类型,死亡率很高。我们报告一例2岁男童的胃肠道毛霉菌病,该患儿表现为腹部肿块,无潜在危险因素。本病例报告的目的是强调其病因发病机制,并在出现腹部肿块的儿童中将毛霉菌病作为鉴别诊断的重点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b0/6811992/94226b1ce1fc/gr1.jpg

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