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BMJ Case Rep. 2017 Oct 4;2017. pii: bcr-2017-221264. doi: 10.1136/bcr-2017-221264.

Safe usage of anakinra and dexamethasone to treat refractory hemophagocytic lymphohistiocytosis secondary to acute disseminated histoplasmosis in a patient with HIV/AIDS.

Author information

1
Division of Rheumatology, Department of Medicine, Albany Medical Center, Albany, New York, USA.
2
Division of Infectious Disease, Department of Medicine, Albany Medical Center, Albany, New York, USA.
3
Department of Internal Medicine, Albany Medical Center, Albany, New York, USA.

Abstract

Hemophagocytic lymphohistiocytosis (HLH) is a serious life-threatening disease if not recognised early. In patients with HIV/AIDS, this association has been reported following acute opportunistic infections, including histoplasmosis. However, optimal treatment is not known. We describe a male aged 46 years with AIDS who developed HLH following acute disseminated histoplasmosis. Presenting symptoms included fever, hepatosplenomegaly and pancytopenia. Bone marrow biopsy confirmed HLH. Initially, he was refractory to the treatment with amphotericin B, antiretroviral therapy and intravenous immunoglobulin (IVIG). Anakinra, an interleukin-1 receptor antagonist, and dexamethasone were initiated. He improved clinically, did not exhibit any harmful effects and ultimately was discharged from the hospital. This, we believe, is the first reported treatment of HLH with anakinra in a patient with AIDS and acute disseminated histoplasmosis.

KEYWORDS:

biological agents; haematology (incl blood transfusion); hiv / aids; rheumatology

PMID:
28978596
DOI:
10.1136/bcr-2017-221264
[Indexed for MEDLINE]

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