Secondary hemophagocytic lymphohistiocytosis due to miliary tuberculosis: diagnostic challenge and therapeutic dilemma

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DOI:

https://doi.org/10.32818/reccmi.a9n2a10

Keywords:

hemophagocytic lymphohistiocytosis, pancytopenia, miliary tuberculosis, immune reconstitution inflammatory syndrome

Abstract

Hemophagocytic syndrome or lymphohistiocytosis hemophagocytic is a severe syndrome of excessive immune activation. We present a case study of hemophagocytic lymphohistiocytosis with severe pancytopenia due to miliary tuberculosis in a 62-year-old woman. During the antituberculosis treatment, the patient experienced radiological worsening, which was likely due to an immune reconstitution inflammatory syndrome. This case highlights on the importance of considering tuberculosis as a potential trigger and, if suspected, antituberculosis therapy should be initiated early, even in the absence of a definitive diagnosis.

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Published

2024-08-26

How to Cite

1.
Delgado-Gómez M, Muñoz-Hernández M, Sáez-García M Ángel, Gómez-Berrocal A. Secondary hemophagocytic lymphohistiocytosis due to miliary tuberculosis: diagnostic challenge and therapeutic dilemma. Rev Esp Casos Clin Med Intern [Internet]. 2024 Aug. 26 [cited 2024 Sep. 1];9(2):71-4. Available from: https://www.reccmi.com/RECCMI/article/view/996