Hemophagocytic lymphohistiocytosis secondary to disseminated histoplasmosis in a renal transplant patient with systemic lupus erythematosus
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Keywords

Hemophagocytic lymphohistiocytosis
Systemic lupus erythematosus
Histoplasma capsulatum
Histoplasmosis
Kidney transplantation

How to Cite

1.
Monroy López LM, Polo Gómez I, Ramos Rincón ML, Martínez Castilla CA, Rodríguez Gómez JC, Rubio Gómez AV, Viñas Granadillo Álvaro J. Hemophagocytic lymphohistiocytosis secondary to disseminated histoplasmosis in a renal transplant patient with systemic lupus erythematosus. Rev. Colomb. Nefrol. [Internet]. 2026 May 28 [cited 2026 Aug. 15];13(1). Available from: https://revistanefrologia.org/index.php/rcn/article/view/997

Abstract

Background: Hemophagocytic lymphohistiocytosis (HLH) is a rare and life-threatening hyperinflammatory syndrome, particularly in immunosuppressed patients such as renal transplant recipients.

Objective: To describe a case of HLH secondary to disseminated histoplasmosis in a patient with systemic lupus erythematosus and kidney transplantation.

Case presentation: We report the case of a 31-year-old male with systemic lupus erythematosus and renal transplantation who presented with persistent fever and pancytopenia. Clinical, microbiological, and bone marrow studies were performed.

Discussion and conclusion: The patient met diagnostic criteria for HLH, with evidence of hemophagocytosis and infection by Histoplasma capsulatum. Treatment with liposomal amphotericin B followed by isavuconazole led to favorable clinical and hematological recovery.

https://doi.org/10.22265/acnef.13.1.997
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