Literature DB >> 31818895

Visceral leishmaniasis presenting as haemophagocytic lymphohistiocytosis.

Lewis Vanhinsbergh1, Aaron Mason2, Andrew Godfrey2.   

Abstract

A 53-year-old man presented with a number of hospital admissions for investigation of fever of unknown origin. He became gradually weaker with significant weight loss, pancytopenia and progressive splenomegaly over a 6-month period of extensive investigation. This was undertaken at different NHS hospitals with involvement of multiple medical specialists. Clinical criteria for haemophagocytic lymphohistiocytosis were met. Following investigation, this was felt likely secondary to a low-grade lymphoma of the spleen, necessitating splenectomy for diagnostic and therapeutic purposes. Ultimately, this risky surgical procedure was avoided when positive L eishmania serology led to successful treatment with amphotericin B. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  haematology (incl blood transfusion); infectious diseases

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Year:  2019        PMID: 31818895     DOI: 10.1136/bcr-2019-232576

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  2 in total

1.  Hemophagocytic lymphohistiocytosis presented with fever of unknown origin: A case study and literature review.

Authors:  Atousa Hakamifard; Masoud Mardani; Tahereh Gholipur-Shahraki
Journal:  Clin Case Rep       Date:  2021-03-08

2.  Fever of unknown origin (FUO) in children: a single-centre experience from Beijing, China.

Authors:  Bing Hu; Tian-Ming Chen; Shu-Ping Liu; Hui-Li Hu; Ling-Yun Guo; He-Ying Chen; Shao-Ying Li; Gang Liu
Journal:  BMJ Open       Date:  2022-03-16       Impact factor: 2.692

  2 in total

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