Hemophagocytic lymphohistiocytosis secondary to AIDS-related histoplasmosis and visceral leishmaniasis

被引：2

作者：

Tomaino, Maria, V ^{[1
]}

Barletta, Jose A. E. ^{[1
]}

Andreani, Mariana ^{[2
]}

Sisto, Alicia ^{[1
]}

Abusamra, Lorena ^{[1
]}

Guelfand, Liliana ^{[2
]}

Rolon, Maria J. ^{[1
]}

机构：

[1] Hosp Juan A Fernandez, Div Infect Dis, Buenos Aires, DF, Argentina

[2] Hosp Juan A Fernandez, Microbiol Sect, Buenos Aires, DF, Argentina

来源：

INTERNATIONAL JOURNAL OF STD & AIDS | 2022年 / 33卷 / 09期

关键词：

HIV (Human immunodeficiency virus) < Viral disease; AIDS < Viral disease; DIAGNOSIS; PATHOPHYSIOLOGY; GUIDELINES;

D O I：

10.1177/09564624221110986

中图分类号：

R392 [医学免疫学]; Q939.91 [免疫学];

学科分类号：

100102 ;

摘要：

Hemophagocytic Lymphohistiocytosis (HLH) is a rare, highly aggressive syndrome involving dysregulated immune response. Most cases are secondary to underlying diseases including infections, autoimmune disorders and malignancies. The burden of disease of histoplasmosis and leishmaniosis associated with advanced HIV is still significant in low-and-middle income countries (LMIC). We present a case of histoplasmosis and leishmaniasis associated HLH in a man with an AIDS diagnosis.

引用

页码：873 / 876

页数：4

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