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本文引用的文献

1
Gastrointestinal mucormycosis: an evolving disease.胃肠道毛霉病:一种不断演变的疾病。
Gastroenterol Hepatol (N Y). 2012 Feb;8(2):140-2.
2
Taxonomy of fungi causing mucormycosis and entomophthoramycosis (zygomycosis) and nomenclature of the disease: molecular mycologic perspectives.真菌引起的毛霉病和虫霉病(接合菌病)的分类学和疾病的命名:分子真菌学观点。
Clin Infect Dis. 2012 Feb;54 Suppl 1(Suppl 1):S8-S15. doi: 10.1093/cid/cir864.
3
Combination therapy for mucormycosis: why, what, and how?联合治疗毛霉病:为什么、用什么、怎么用?
Clin Infect Dis. 2012 Feb;54 Suppl 1(Suppl 1):S73-8. doi: 10.1093/cid/cir885.
4
A global analysis of mucormycosis in France: the RetroZygo Study (2005-2007).法国毛霉病的全球分析:RetroZygo 研究(2005-2007 年)。
Clin Infect Dis. 2012 Feb;54 Suppl 1:S35-43. doi: 10.1093/cid/cir880.
5
Epidemiology and clinical manifestations of mucormycosis.毛霉病的流行病学和临床表现。
Clin Infect Dis. 2012 Feb;54 Suppl 1:S23-34. doi: 10.1093/cid/cir866.
6
The Deferasirox-AmBisome Therapy for Mucormycosis (DEFEAT Mucor) study: a randomized, double-blinded, placebo-controlled trial.去铁酮-两性霉素 B 脂质体治疗毛霉病(DEFEAT Mucor)研究:一项随机、双盲、安慰剂对照试验。
J Antimicrob Chemother. 2012 Mar;67(3):715-22. doi: 10.1093/jac/dkr375. Epub 2011 Sep 20.
7
Molecular tools for identification of Zygomycetes and the diagnosis of zygomycosis.用于鉴定接合菌纲及诊断接合菌病的分子工具。
Clin Microbiol Infect. 2009 Oct;15 Suppl 5:66-70. doi: 10.1111/j.1469-0691.2009.02983.x.
8
Recent advances in the management of mucormycosis: from bench to bedside.毛霉菌病治疗的最新进展:从实验室到临床
Clin Infect Dis. 2009 Jun 15;48(12):1743-51. doi: 10.1086/599105.
9
Posaconazole mono- or combination therapy for treatment of murine zygomycosis.泊沙康唑单药或联合治疗小鼠接合菌病。
Antimicrob Agents Chemother. 2009 Feb;53(2):772-5. doi: 10.1128/AAC.01124-08. Epub 2008 Oct 20.
10
Detection of a molecular biomarker for zygomycetes by quantitative PCR assays of plasma, bronchoalveolar lavage, and lung tissue in a rabbit model of experimental pulmonary zygomycosis.通过对实验性肺接合菌病兔模型的血浆、支气管肺泡灌洗和肺组织进行定量PCR检测来检测接合菌的分子生物标志物。
J Clin Microbiol. 2008 Nov;46(11):3690-702. doi: 10.1128/JCM.00917-08. Epub 2008 Sep 24.

“人如其食!”侵袭性肠道毛霉菌病:一例报告及文献综述

"We are what we eat!" Invasive intestinal mucormycosis: A case report and review of the literature.

作者信息

Martinello Marianne, Nelson Adam, Bignold Leon, Shaw David

机构信息

Royal Adelaide Hospital, North Terrace, Adelaide, South Australia, Australia.

Institute of Medical and Veterinary Science, Frome Road, Adelaide, South Australia, Australia.

出版信息

Med Mycol Case Rep. 2012 Aug 4;1(1):52-5. doi: 10.1016/j.mmcr.2012.07.003. eCollection 2012.

DOI:10.1016/j.mmcr.2012.07.003
PMID:24371738
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3855875/
Abstract

Gastrointestinal mucormycosis is an uncommon, life-threatening, angioinvasive infection with only one previous report of disease involving the jejunum. We present a case of invasive jejunal mucormycosis and review the literature, highlighting the rare clinical presentation and the value of molecular diagnostic methods. Given the global increase in patient populations at risk of mucormycosis, clinicians need to maintain a high index of suspicion and perform timely and appropriate evaluation to improve patient outcome.

摘要

胃肠道毛霉病是一种罕见的、危及生命的血管侵袭性感染,此前仅有一例累及空肠的病例报告。我们报告一例侵袭性空肠毛霉病病例并复习文献,强调其罕见的临床表现及分子诊断方法的价值。鉴于全球毛霉病高危患者人群增加,临床医生需要保持高度警惕,及时进行恰当评估以改善患者预后。