Bone marrow histoplasmosis-the hidden culprit in an immunodeficiency setting

A 30-year-old male patient presented with complaints of fever, anorexia and hepatosplenomegaly for the past 3 months. He was seropositive for hepatitis C (HCV) and human immunodeficiency virus (HIV).

Laboratory investigation revealed pancytopenia with altered liver function.

Bone marrow aspirate and imprint smears appeared deceptively clean without a reactive background that one would expect in an infectious setting. A diligent search revealed an occasional macrophage showing intracellular oval globose yeast-like cells with a clear space or halo around the eccentrically placed nucleus. Haematoxylin and Eosin-stained sections of trephine biopsy showed similar organisms (Figure 1). So, the diagnosis of Histoplasmosis was made. The patient responded effectively to antifungal drugs (Amphotericin B).

Figure 1
. Giemsa-stained imprint smear shows intracellular Histoplasma sp. in otherwise unremarkable bone marrow (arrow)(1000x) [A]. Bone marrow biopsy of the same patient shows similar intracellular organisms (1000x), the morphological hint being eccentricity of the nucleus. However, the thick cell wall is better appreciated in cytology smears [B].

Histoplasmosis is a systemic fungal infection caused by the dimorphic fungus Histoplasma capsulatum. The causative fungus persists in soil, infects through inhalation and manifests in three main types - acute primary, chronic cavitary and progressive disseminated histoplasmosis. In India, the disease is endemic in the eastern part of the country.¹

• Funding information
  No funding was received for this study.

Reference

• ¹
  Samaddar A., Sharma A., Kumar P.H .A, Srivastava S., Shrimali T., Gopalakrishnan M., et al. Disseminated histoplasmosis in immunocompetent patients from an arid zone in Western India: a case series. Med Mycol Case Rep. 2019;25(July):49-52.

Publication Dates

• Publication in this collection
  27 May 2024
• Date of issue
  Jan-Mar 2024

History

• Received
  16 Sept 2022
• Accepted
  28 May 2023
• Published
  31 July 2023