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本文引用的文献

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Review of haemophagocytic lymphohistiocytosis.噬血细胞性淋巴组织细胞增生症综述。
Arch Dis Child. 2011 Jul;96(7):688-93. doi: 10.1136/adc.2009.176610. Epub 2010 Jun 28.
2
Leukopenic Myelosis: (Section of Medicine).白细胞减少性骨髓组织增生症:(医学科)
Proc R Soc Med. 1939 Sep;32(11):1429-34. doi: 10.1177/003591573903201147.
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
Hemophagocytic lymphohistiocytosis associated with visceral leishmaniasis.与内脏利什曼病相关的噬血细胞性淋巴组织细胞增生症。
J Trop Pediatr. 2007 Oct;53(5):359-61. doi: 10.1093/tropej/fmm024. Epub 2007 Jul 11.
5
HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.HLH-2004:噬血细胞性淋巴组织细胞增生症的诊断与治疗指南。
Pediatr Blood Cancer. 2007 Feb;48(2):124-31. doi: 10.1002/pbc.21039.
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Performance of recombinant K39 antigen in the diagnosis of Brazilian visceral leishmaniasis.重组K39抗原在巴西内脏利什曼病诊断中的性能
Am J Trop Med Hyg. 2003 Mar;68(3):321-4.
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Hemophagocytic syndrome: a rare life-threatening complication of visceral leishmaniasis in a young boy.噬血细胞综合征:一名小男孩内脏利什曼病罕见的危及生命的并发症。
Pediatr Hematol Oncol. 2001 Dec;18(8):531-6. doi: 10.1080/088800101753328501.
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Influence of liposomal amphotericin B on CD8 T-cell function.脂质体两性霉素B对CD8 T细胞功能的影响。
Antimicrob Agents Chemother. 2001 Aug;45(8):2383-5. doi: 10.1128/AAC.45.8.2383-2385.2001.
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Hemophagocytic lymphohistiocytosis associated with visceral leishmaniasis.与内脏利什曼病相关的噬血细胞性淋巴组织细胞增生症
Pediatr Hematol Oncol. 2001 Jan-Feb;18(1):65-70. doi: 10.1080/088800101750059873.
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[Intravenously administered gamma-globulins in reactive hemaphagocytic syndrome. Multicenter study to assess their importance, by the immunoglobulins group of experts of CEDIT of the AP-HP].[静脉注射丙种球蛋白治疗反应性噬血细胞综合征。巴黎公立医院协会临床与研究信息中心免疫球蛋白专家小组进行的多中心研究以评估其重要性]
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成人晚期内脏利什曼病相关噬血细胞性淋巴组织细胞增生症。

Hemophagocytic lymphohistiocytosis associated with visceral leishmaniasis in late adulthood.

机构信息

Hospital das Clínicas da Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.

出版信息

Am J Trop Med Hyg. 2013 Mar;88(3):575-7. doi: 10.4269/ajtmh.12-0563. Epub 2013 Jan 16.

DOI:10.4269/ajtmh.12-0563
PMID:23324220
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3592544/
Abstract

We describe a case of hemophagocytic lymphohistiocytosis related to visceral leishmaniasis in late adulthood. Because clinical features of visceral leishmaniasis can mimic those of hemophagocytic lymphohistiocytosis, diagnosing leishmaniasis as the underlying etiology can be quite challenging. In our case, treatment with amphotericin B resulted in a dramatic resolution of clinical abnormalities.

摘要

我们描述了一例发生于成年晚期的与内脏利什曼病相关的噬血细胞性淋巴组织细胞增生症。由于内脏利什曼病的临床特征可类似于噬血细胞性淋巴组织细胞增生症,因此诊断利什曼病为潜在病因颇具挑战性。在我们的病例中,两性霉素 B 治疗导致临床异常显著缓解。