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本文引用的文献

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Studies on the pancytopenia of kala-azar.黑热病全血细胞减少症的研究。
Blood. 1948 Mar;3(3):249-75.
2
Evaluation of direct agglutination test, rk39 Test, and ELISA for the diagnosis of visceral leishmaniasis.评价直接凝集试验、rk39试验和酶联免疫吸附测定法用于内脏利什曼病的诊断。
Am J Trop Med Hyg. 2008 Jul;79(1):76-8.
3
Visceral leishmaniasis associated hemophagocytic lymphohistiocytosis--case report and systematic review.内脏利什曼病相关噬血细胞性淋巴组织细胞增生症——病例报告及系统综述
J Infect. 2008 May;56(5):381-8. doi: 10.1016/j.jinf.2008.02.013. Epub 2008 Apr 10.
4
Fatal haemophagocytic syndrome and hepatitis associated with visceral leishmaniasis.与内脏利什曼病相关的致命性噬血细胞综合征和肝炎。
Indian J Med Microbiol. 2007 Oct;25(4):416-8. doi: 10.4103/0255-0857.37354.
5
Immune response to leishmania: paradox rather than paradigm.对利什曼原虫的免疫反应:是悖论而非范例。
FEMS Immunol Med Microbiol. 2007 Nov;51(2):229-42. doi: 10.1111/j.1574-695X.2007.00311.x. Epub 2007 Aug 22.
6
Kala-azar--progress against a neglected disease.黑热病——抗击一种被忽视疾病的进展
N Engl J Med. 2002 Nov 28;347(22):1793-4. doi: 10.1056/NEJMe020133.
7
Leishmania donovani infection of bone marrow stromal macrophages selectively enhances myelopoiesis, by a mechanism involving GM-CSF and TNF-alpha.杜氏利什曼原虫感染骨髓基质巨噬细胞可通过一种涉及粒细胞-巨噬细胞集落刺激因子(GM-CSF)和肿瘤坏死因子-α(TNF-α)的机制选择性增强骨髓生成。
Blood. 2000 Mar 1;95(5):1642-51.
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Leishmaniasis.利什曼病
Lancet. 1999 Oct 2;354(9185):1191-9. doi: 10.1016/S0140-6736(98)10178-2.
9
Visceral leishmaniasis: III. Effect of parasitaemia level on the bone marrow ultrastructure.内脏利什曼病:III. 寄生虫血症水平对骨髓超微结构的影响。
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内脏利什曼病/黑热病中的血液学变化

Hematologic changes in visceral leishmaniasis/kala azar.

作者信息

Varma Neelam, Naseem Shano

出版信息

Indian J Hematol Blood Transfus. 2010 Sep;26(3):78-82. doi: 10.1007/s12288-010-0027-1. Epub 2010 Sep 30.

DOI:10.1007/s12288-010-0027-1
PMID:21886387
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3002089/
Abstract

Visceral Leishmaniasis (VL) or Kala Azar is a chronic infectious disease caused by parasites of the Leishmania donovani complex that can cause various hematologic manifestations. It is characterized by fever, enlargement of liver and spleen, weight loss, pancytopenia and hypergammaglobinemia. It is endemic in the Indian subcontinent, mainly seen in the states of Bihar and West Bengal. Patients with VL can present to the haematologist for various haematological problems prior to receiving the diagnosis of VL. Anaemia is the most common haematological manifestation of VL. VL may also be associated with leucopenia, thrombocytopenia, pancytopenia, hemophagocytosis and disseminated intravascular coagulation. Hematological improvement is noted within a week and complete hematological response occurs in 4-6 weeks of treatment. Relapses are rare and increased risk of being diagnosed with hematolymphoid malignancies on long term follow up is not noted.

摘要

内脏利什曼病(VL)或黑热病是一种由杜氏利什曼原虫复合体寄生虫引起的慢性传染病,可导致各种血液学表现。其特征为发热、肝脾肿大、体重减轻、全血细胞减少和高球蛋白血症。该病在印度次大陆为地方性疾病,主要见于比哈尔邦和西孟加拉邦。VL患者在确诊VL之前可能因各种血液学问题就诊于血液科医生。贫血是VL最常见的血液学表现。VL还可能与白细胞减少、血小板减少、全血细胞减少、噬血细胞增多和弥散性血管内凝血有关。治疗一周内可观察到血液学改善,4 - 6周出现完全血液学反应。复发罕见,长期随访未发现患血液淋巴系统恶性肿瘤的风险增加。