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小肠结肠炎耶尔森菌败血症

Yersinia enterocolitica Septicemia.

作者信息

Bouza E, Dominguez A, Meseguer M, Buzon L, Boixeda D, Revillo M J, de Rafael L, Martinez-Beltran J

出版信息

Am J Clin Pathol. 1980 Oct;74(4):404-9. doi: 10.1093/ajcp/74.4.404.

DOI:10.1093/ajcp/74.4.404
PMID:7424822
Abstract

Human Yersinia enterocolitica septicemia is an uncommon condition. Four new cases are reported here and a review is made of 51 others taken from medical literature. Septicemia caused by this microorganism occurs more frequently in the young and in the elderly, and usually involves patients havig previous liver or blood disorders, diabetes mellitus, and other debilitating diseases. Clinically it is indistinguishable from sepsis caused by other organisms of Enterobacteriaceae, but it is important that the clinician bear its existence in mind, since Yersinia enterocolitica strains are usually resistant to beta-lactam antibiotics, whereas they are susceptible to the aminoglycosides and co-trimoxazole, among others. Susceptibilities in the blood isolates from our patients, and in another ten fecal isolates from eight other patients showed the previously described pattern. Our isolates, however, were all susceptible to the new cephalosporins, cefamandole and cefoxitin, and to the experimental ones, HR-756, T-1551, and Ly-127.935.

摘要

人类小肠结肠炎耶尔森菌败血症是一种罕见病症。本文报告了4例新病例,并对医学文献中另外51例病例进行了综述。这种微生物引起的败血症在年轻人和老年人中更为常见,通常累及先前有肝脏或血液疾病、糖尿病及其他衰弱性疾病的患者。临床上,它与由其他肠杆菌科细菌引起的败血症难以区分,但临床医生必须牢记其存在,因为小肠结肠炎耶尔森菌菌株通常对β-内酰胺类抗生素耐药,而对氨基糖苷类和复方新诺明等敏感。我们患者血液分离株以及另外8例患者的10份粪便分离株的药敏情况显示出上述模式。然而,我们的分离株对新型头孢菌素头孢孟多和头孢西丁以及实验性药物HR-756、T-1551和Ly-127.935均敏感。

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1
Yersinia enterocolitica Septicemia.小肠结肠炎耶尔森菌败血症
Am J Clin Pathol. 1980 Oct;74(4):404-9. doi: 10.1093/ajcp/74.4.404.
2
[Septicemia caused by Yersinia enterocolitica. General review apropos of a new case in a young women presenting with thalassemia major].[小肠结肠炎耶尔森菌引起的败血症。关于一名患有重型地中海贫血的年轻女性的新病例的综述]
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[Severe septicemia caused by Yersinia enterocolitica].小肠结肠炎耶尔森菌引起的严重败血症
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Yersinia enterocolitica septicemia.小肠结肠炎耶尔森菌败血症
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引用本文的文献

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Yersinia enterocolitica Septicemia After Chitterling Ingestion in a Pediatric Patient With Iron Overload Disease: A Case Report.一名患有铁过载疾病的儿科患者因食用猪小肠后发生小肠结肠炎耶尔森菌败血症:病例报告
Glob Pediatr Health. 2015 Jun 23;2:2333794X15592611. doi: 10.1177/2333794X15592611. eCollection 2015.
2
Spontaneous Yersinia enterocolitica septicemia in a patient with iron overload.一名铁过载患者发生自发性小肠结肠炎耶尔森菌败血症。
Can J Infect Dis. 1990 Summer;1(2):57-60. doi: 10.1155/1990/671489.
3
Protective roles for fibrin, tissue factor, plasminogen activator inhibitor-1, and thrombin activatable fibrinolysis inhibitor, but not factor XI, during defense against the gram-negative bacterium Yersinia enterocolitica.
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J Immunol. 2011 Aug 15;187(4):1866-76. doi: 10.4049/jimmunol.1101094. Epub 2011 Jul 1.
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YspM, a newly identified Ysa type III secreted protein of Yersinia enterocolitica.YspM,一种新鉴定出的小肠结肠炎耶尔森菌的YsaⅢ型分泌蛋白。
J Bacteriol. 2008 Nov;190(22):7315-25. doi: 10.1128/JB.00861-08. Epub 2008 Sep 19.
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Characterization of a novel porin involved in systemic Yersinia enterocolitica infection.参与小肠结肠炎耶尔森菌全身感染的一种新型孔蛋白的特性分析
Infect Immun. 2006 Jul;74(7):4361-5. doi: 10.1128/IAI.00154-06.
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Tumor necrosis factor receptor p55-deficient mice respond to acute Yersinia enterocolitica infection with less apoptosis and more effective host resistance.肿瘤坏死因子受体p55缺陷型小鼠对急性小肠结肠炎耶尔森菌感染的反应是凋亡减少,宿主抵抗力增强。
Infect Immun. 2000 Mar;68(3):1243-51. doi: 10.1128/IAI.68.3.1243-1251.2000.
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Yersinia-induced apoptosis in vivo aids in the establishment of a systemic infection of mice.耶尔森氏菌在体内诱导的细胞凋亡有助于小鼠全身性感染的建立。
J Exp Med. 1998 Dec 7;188(11):2127-37. doi: 10.1084/jem.188.11.2127.
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In vivo tracking and protective properties of Yersinia-specific intestinal T cells.耶尔森菌特异性肠道T细胞的体内追踪及保护特性
Clin Exp Immunol. 1998 Sep;113(3):429-37. doi: 10.1046/j.1365-2249.1998.00659.x.
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Ambiguous role of interleukin-12 in Yersinia enterocolitica infection in susceptible and resistant mouse strains.白细胞介素-12在易感和抗性小鼠品系小肠结肠炎耶尔森菌感染中的作用不明确。
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Yersinia enterocolitica: the charisma continues.小肠结肠炎耶尔森菌:魅力依旧。
Clin Microbiol Rev. 1997 Apr;10(2):257-76. doi: 10.1128/CMR.10.2.257.