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Case Report: Hemophagocytic Lymphohistiocytosis Caused by Disseminated Histoplasmosis in a Venezuelan Patient with HIV and Epstein–Barr Virus Reactivation Who Traveled to Japan
Author(s) -
Motoyuki Tsuboi,
Takeshi Nishijima,
Minoru Nagi,
Yoshitsugu Miyazaki,
Katsuji Teruya,
Yoshimi Kikuchi,
Hiroyuki Gatanaga,
Shinichi Oka
Publication year - 2019
Publication title -
american journal of tropical medicine and hygiene
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.015
H-Index - 151
eISSN - 1476-1645
pISSN - 0002-9637
DOI - 10.4269/ajtmh.18-0478
Subject(s) - hemophagocytic lymphohistiocytosis , histoplasmosis , medicine , virology , epstein–barr virus , human immunodeficiency virus (hiv) , virus , immunology , pathology , disease
We describe a Venezuelan visitor to Japan who was diagnosed with hemophagocytic lymphohistiocytosis (HLH). The patient was also diagnosed with human immunodeficiency virus (HIV) and Epstein-Barr virus infection by the Western blot and polymerase chain reaction (PCR) tests, respectively. The cause of HLH was considered to be these two infections at first; however, the patient did not recover with antiretroviral/anti-herpes virus therapy. Thereafter, diagnosis of disseminated histoplasmosis was confirmed with an antigen detection test, culture, and PCR test of blood, urine, and bone marrow, and the patient improved gradually after the initiation of liposomal amphotericin B. This case highlights the importance of ruling out endemic mycosis as a cause of HLH even if other probable causes exist in patients from endemic areas.

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