A Review of Hemophagocytic Lymphohistiocytosis in Patients With HIV

被引:30
作者
Tabaja, Hussam [1 ]
Kanj, Amjad [2 ]
El Zein, Said [1 ]
Comba, Isin Yagmur [1 ]
Chehab, Omar [3 ]
Mahmood, Maryam [1 ]
机构
[1] Mayo Clin, Div Infect Dis, Rochester, MN 55905 USA
[2] Mayo Clin, Div Pulm & Crit Care Med, Rochester, MN 55905 USA
[3] Johns Hopkins Univ, Div Internal Med, Baltimore, MD USA
关键词
AIDS; hemophagocytosis; HIV; lymphohistiocytosis; ACQUIRED-IMMUNODEFICIENCY-SYNDROME; DISSEMINATED HISTOPLASMOSIS; AIDS PATIENT; INFECTION; DIAGNOSIS; LYMPHOMA; CYTOMEGALOVIRUS; GUIDELINES; SECONDARY; SARCOMA;
D O I
10.1093/ofid/ofac071
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We provide an elaborate review of cases published between January 2005 and April 2021 on hemophagocytic lymphohistiocytosis (HLH) in HIV patients. Seventy articles describing 81 adult patients (age >= 19 years) were included. The median age was 40 years, and 78% were males. Only 65% were known to have HIV before presentation. CD4 count was >= 200 cells/mm(3) in 23%, and HIV viral load was <200 copies/mL in 41%. The lack of meticulous reporting of >= 5 of 8 criteria for HLH diagnosis was evident in a third of cases. At least 1 infectious agent-other than HIV-was believed to trigger HLH in 78% of patients. The most common were Epstein-Barr virus (26%), human herpesvirus 8 (21%), and Histoplasma capsulatum (17%). Sixty percent survived. Among those, 93% received treatment for identified secondary trigger(s), while 51% received HLH-directed therapy. There was significant heterogeneity in the treatment regimens used for HLH.
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页数:10
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