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Clin Infect Dis. 2016 Aug 15;63(4):433-42. doi: 10.1093/cid/ciw444.
2
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Mycopathologia. 2014 Apr;177(3-4):187-92. doi: 10.1007/s11046-014-9733-9. Epub 2014 Feb 26.
3
Preliminary laboratory report of fungal infections associated with contaminated methylprednisolone injections.初步实验室报告:与污染的甲基强的松龙注射液相关的真菌感染。
J Clin Microbiol. 2013 Aug;51(8):2654-61. doi: 10.1128/JCM.01000-13. Epub 2013 Jun 12.
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[Fatal zygomycosis caused by Mucor indicus after haplo-identical stem cell transplantation].[单倍体相合干细胞移植后由印度毛霉引起的致死性接合菌病]
Rinsho Ketsueki. 2013 Mar;54(3):311-5.
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Trends in zygomycosis in children.儿童接合菌病的流行趋势。
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Clinical practice guideline for the use of antimicrobial agents in neutropenic patients with cancer: 2010 update by the infectious diseases society of america.抗菌药物在肿瘤中性粒细胞减少患者应用的临床实践指南:美国传染病学会 2010 年更新版。
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一名儿童骨髓移植受者中由米根毛霉引起的坏死性筋膜炎。

Necrotizing fasciitis caused by Mucor indicus in a pediatric bone marrow transplant recipient.

作者信息

Bloch Deborah, Gonzalez Mark D, Haight Ann, Abramowsky Carlos, Yildirim Inci

机构信息

Department of Pediatric Infectious Diseases, Emory University, Atlanta, Georgia.

Microbiology Laboratory, Children's Healthcare of Atlanta, Atlanta, Georgia.

出版信息

Pediatr Transplant. 2018 Dec;22(8):e13294. doi: 10.1111/petr.13294. Epub 2018 Sep 23.

DOI:10.1111/petr.13294
PMID:30246483
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6460914/
Abstract

Necrotizing fasciitis is a life-threatening, rapidly progressing infection of fascia and subcutaneous cellular tissue typically caused by mixed aerobic and anaerobic bacteria. We present a case report of an immunocompromised 4-year-old female with necrotizing fasciitis from a rare fungal organism, Mucor indicus. The patient underwent multiple debridements and was treated for 10 months, first on liposomal amphotericin B (2 months) then posaconazole (8 months). Mucor indicus is a rarely described pathogen with only nine other cases described. Identification of this organism remains a challenge, and the need for further understanding of risk factors and organism susceptibility testing to help guide treatment is crucial.

摘要

坏死性筋膜炎是一种危及生命、进展迅速的筋膜和皮下蜂窝组织感染,通常由需氧菌和厌氧菌混合感染引起。我们报告一例免疫功能低下的4岁女性坏死性筋膜炎病例,其病原菌为一种罕见的真菌——印度毛霉。该患者接受了多次清创手术,并接受了10个月的治疗,最初使用脂质体两性霉素B治疗2个月,然后使用泊沙康唑治疗8个月。印度毛霉是一种很少被描述的病原体,此前仅另有9例病例报道。识别这种病原体仍然是一项挑战,进一步了解危险因素和进行病原体药敏试验以指导治疗至关重要。