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Front Cell Infect Microbiol. 2023 Feb 7;13:1089196. doi: 10.3389/fcimb.2023.1089196. eCollection 2023.
2
Gastric mucormycosis complicated by a gastropleural fistula: A case report and review of the literature.胃毛霉病合并胃胸膜瘘:一例病例报告及文献复习
Medicine (Baltimore). 2019 Nov;98(48):e18142. doi: 10.1097/MD.0000000000018142.
3
Necrotizing fasciitis caused by Mucor indicus in a pediatric bone marrow transplant recipient.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。
Pediatr Transplant. 2018 Dec;22(8):e13294. doi: 10.1111/petr.13294. Epub 2018 Sep 23.
4
Mucormycosis in Children: Review and Recommendations for Management.儿童毛霉菌病:治疗管理的综述和建议。
J Pediatric Infect Dis Soc. 2018 May 15;7(2):159-164. doi: 10.1093/jpids/pix107.
5
Successful treatment of a necrotizing fasciitis patient caused by Mucor indicus with amphotericin B and skin grafting.成功应用两性霉素 B 和植皮治疗由印度毛霉引起的坏死性筋膜炎。
Mycopathologia. 2014 Apr;177(3-4):187-92. doi: 10.1007/s11046-014-9733-9. Epub 2014 Feb 26.
6
[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.
7
Mucor indicus: biology and industrial application perspectives: a review.印度毛霉:生物学及工业应用展望——综述
Biotechnol Adv. 2013 Jul-Aug;31(4):466-81. doi: 10.1016/j.biotechadv.2013.01.009. Epub 2013 Jan 31.
8
Healthcare-associated mucormycosis.医疗机构相关性毛霉病。
Clin Infect Dis. 2012 Feb;54 Suppl 1:S44-54. doi: 10.1093/cid/cir867.
9
Spectrum of zygomycete species identified in clinically significant specimens in the United States.在美国具有临床意义的标本中鉴定出的接合菌物种谱。
J Clin Microbiol. 2009 Jun;47(6):1650-6. doi: 10.1128/JCM.00036-09. Epub 2009 Apr 22.
10
Fatal zygomycosis caused by Mucor indicus in a child with an implantable left ventricular assist device.一名植入左心室辅助装置的儿童因米根霉引发致命性接合菌病。
Pediatr Infect Dis J. 2008 Apr;27(4):365-9. doi: 10.1097/INF.0b013e3181634f2b.

一名因短肠综合征接受长期肠外营养的5岁儿童反复发生中心静脉导管感染:肠道细菌易位是病因吗?

Recurrent  central venous catheter infection in a five year old child on long term parenteral nutrition for short gut syndrome: could gut translocation be responsible?

作者信息

Allen Sarah

机构信息

Women's and Children's Hospital, 72 King William Rd, Adelaide, 5006, Australia.

出版信息

Med Mycol Case Rep. 2024 Jul 14;45:100661. doi: 10.1016/j.mmcr.2024.100661. eCollection 2024 Sep.

DOI:10.1016/j.mmcr.2024.100661
PMID:39139261
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11321366/
Abstract

A five year old girl with life-long TPN dependence for short gut syndrome presented with two episodes of non-fatal central line associated blood stream infection (CLABSI). Each episode occurred fifteen months apart, without any evidence of ongoing mould infection whilst off antifungal therapy in the intervening time period. Both episodes were treated with removal of the infected central venous catheter (CVC) and 6 weeks of intravenous liposomal amphotericin B and/or posaconazole, with good clinical, microbiological, and radiological response. The possibility of gut translocation is supported by the repeated isolation of in cases of intestinal mucormycosis. To our knowledge, this is the first case of recurrent episodes of blood culture positive mucormycosis in a single patient. blood stream infection may differ significantly from invasive mucormycosis caused by other species.

摘要

一名因短肠综合征终生依赖全胃肠外营养(TPN)的5岁女孩出现了两例非致命性中心静脉导管相关血流感染(CLABSI)。每例感染相隔15个月发生,在其间停用抗真菌治疗期间,没有任何持续霉菌感染的迹象。两例感染均通过拔除感染的中心静脉导管(CVC)以及6周的静脉注射脂质体两性霉素B和/或泊沙康唑进行治疗,临床、微生物学和影像学反应良好。肠道毛霉病病例中反复分离出[具体内容缺失]支持了肠道细菌易位的可能性。据我们所知,这是首例单一患者反复出现血培养阳性毛霉病的病例。血流感染可能与其他菌种引起的侵袭性毛霉病有显著差异。