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本文引用的文献

1
The systemic pathology of cerebral malaria in African children.非洲儿童脑型疟疾的全身病理学
Front Cell Infect Microbiol. 2014 Aug 21;4:104. doi: 10.3389/fcimb.2014.00104. eCollection 2014.
2
A histological method for quantifying Plasmodium falciparum in the brain in fatal paediatric cerebral malaria.一种用于量化致命性小儿脑型疟中脑内疟原虫感染的组织学方法。
Malar J. 2013 Jun 7;12:191. doi: 10.1186/1475-2875-12-191.
3
Lethal malaria: Marchiafava and Bignami were right.致命性疟疾:Marchiafava 和 Bignami 是对的。
J Infect Dis. 2013 Jul 15;208(2):192-8. doi: 10.1093/infdis/jit116. Epub 2013 Apr 12.
4
Sequestration and microvascular congestion are associated with coma in human cerebral malaria.疟原虫性昏迷与隔离和微血管淤血有关。
J Infect Dis. 2012 Feb 15;205(4):663-71. doi: 10.1093/infdis/jir812. Epub 2011 Dec 29.
5
Coma in fatal adult human malaria is not caused by cerebral oedema.致命性成人疟疾患者的昏迷并非由脑水肿引起。
Malar J. 2011 Sep 17;10:267. doi: 10.1186/1475-2875-10-267.
6
Liver pathology in Malawian children with fatal encephalopathy.马拉维儿童致死性脑病的肝脏病理学。
Hum Pathol. 2011 Sep;42(9):1230-9. doi: 10.1016/j.humpath.2010.11.019. Epub 2011 Mar 10.
7
The distribution and intensity of parasite sequestration in comatose Malawian children.马拉维昏迷儿童体内寄生虫隔离的分布与强度
J Infect Dis. 2006 Jul 15;194(2):208-5. doi: 10.1086/505078. Epub 2006 Jun 13.
8
A quantitative ultrastructural study of the liver and the spleen in fatal falciparum malaria.恶性疟致死病例肝脏与脾脏的定量超微结构研究
Southeast Asian J Trop Med Public Health. 2005 Nov;36(6):1359-70.
9
Fatal Plasmodium falciparum malaria causes specific patterns of splenic architectural disorganization.恶性疟原虫所致的致命性疟疾会引发脾脏结构紊乱的特定模式。
Infect Immun. 2005 Apr;73(4):1986-94. doi: 10.1128/IAI.73.4.1986-1994.2005.
10
Differentiating the pathologies of cerebral malaria by postmortem parasite counts.通过尸检寄生虫计数鉴别脑型疟疾的病理情况。
Nat Med. 2004 Feb;10(2):143-5. doi: 10.1038/nm986. Epub 2004 Jan 25.

致命性儿童脑型疟疾中寄生虫多器官隐匿的定量评估

Quantitative Assessment of Multiorgan Sequestration of Parasites in Fatal Pediatric Cerebral Malaria.

作者信息

Milner Danny A, Lee Jonathan J, Frantzreb Charles, Whitten Richard O, Kamiza Steve, Carr Richard A, Pradham Alana, Factor Rachel E, Playforth Krupa, Liomba George, Dzamalala Charles, Seydel Karl B, Molyneux Malcolm E, Taylor Terrie E

机构信息

Department of Pathology, Brigham and Women's Hospital Department of Immunology and Infectious Disease, Harvard School of Public Health, Boston, Massachusetts Blantyre Malaria Project, University of Malawi College of Medicine.

Department of Pathology, Brigham and Women's Hospital.

出版信息

J Infect Dis. 2015 Oct 15;212(8):1317-21. doi: 10.1093/infdis/jiv205. Epub 2015 Apr 7.

DOI:10.1093/infdis/jiv205
PMID:25852120
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4577044/
Abstract

Children in sub-Saharan Africa continue to acquire and die from cerebral malaria, despite efforts to control or eliminate the causative agent, Plasmodium falciparum. We present a quantitative histopathological assessment of the sequestration of parasitized erythrocytes in multiple organs obtained during a prospective series of 103 autopsies performed between 1996 and 2010 in Blantyre, Malawi, on pediatric patients who died from cerebral malaria and controls. After the brain, sequestration of parasites was most intense in the gastrointestinal tract, both in patients with cerebral malaria and those with parasitemia in other organs. Within cases of histologically defined cerebral malaria, which includes phenotypes termed "sequestration only" (CM1) and "sequestration with extravascular pathology" (CM2), CM1 was associated with large parasite numbers in the spleen and CM2 with intense parasite sequestration in the skin. A striking histological finding overall was the marked sequestration of parasitized erythrocytes across most organs in patients with fatal cerebral malaria, supporting the hypothesis that the disease is, in part, a result of a high level of total-body parasite sequestration.

摘要

尽管人们努力控制或消灭致病原恶性疟原虫,但撒哈拉以南非洲的儿童仍不断感染脑型疟疾并因此死亡。我们对1996年至2010年间在马拉维布兰太尔对死于脑型疟疾的儿科患者及对照进行的103例前瞻性尸检中获取的多个器官内寄生红细胞的滞留情况进行了定量组织病理学评估。除脑部外,脑型疟疾患者以及其他器官有寄生虫血症的患者,胃肠道内的寄生虫滞留最为严重。在组织学定义的脑型疟疾病例中,包括“仅滞留”(CM1)和“伴有血管外病理改变的滞留”(CM2)两种表型,CM1与脾脏中大量寄生虫有关,CM2与皮肤中强烈的寄生虫滞留有关。总体而言,一个显著的组织学发现是,致命性脑型疟疾患者的大多数器官中都有明显的寄生红细胞滞留,这支持了该病部分是全身寄生虫高水平滞留所致的假说。