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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References

La Rosée P, Horne A, Hines M, von Bahr Greenwood T, Machowicz R, Berliner N, et al. Recommendations for the management of hemophagocytic lym¬phohistiocytosis in adults. Blood 2019; 133: 2465–2477. doi: http://dx.doi. org/10.1182/blood.2018894618 (último acceso jun. 2024). DOI: https://doi.org/10.1182/blood.2018894618

Kim YR, Kim DY. Current status of the diagnosis and treatment of hemopha¬gocytic lymphohistiocytosis in adults. Blood Res. 2021; 56(S1): S17-S25. doi: http://dx.doi.org/10.5045/br.2021.2020323 (último acceso jun. 2024). DOI: https://doi.org/10.5045/br.2021.2020323

Hermans SM, Akkerman OW, Meintjes G, Grobusch MP. Post-tuberculo¬sis treatment paradoxical reactions. Infection. 2024; doi: http://dx.doi. org/10.1007/s15010-024-02310-0 (último acceso jul. 2024). DOI: https://doi.org/10.1007/s15010-024-02310-0

Kurver L, Seers T, van Dorp S, van Crevel R, Pollara G, van Laarhoven A. Tuberculosis-associated hemophagocytic lymphohistiocytosis: Diag¬nostic challenges and determinants of outcome. Open Forum Infect Dis. 2024; 11(4): ofad697. doi: https://academic.oup.com/ofid/article/11/4/ ofad697/7516258 (último acceso jun. 2024). DOI: https://doi.org/10.1093/ofid/ofad697

Zhang Y, Liang G, Qin H, Li Y, Zeng X. Tuberculosis-associated hemophago¬cytic lymphohistiocytosis with initial presentation of fever of unknown ori¬gin in a general hospital: An analysis of 8 clinical cases. Medicine (Baltimore). 2017; 96(16): e6575. doi: http://dx.doi.org/10.1097/md.0000000000006575 (último acceso jun. 2024). DOI: https://doi.org/10.1097/MD.0000000000006575

Mert A, Arslan F, Kuyucu T, Koç EN, Yilmaz M, Turan D, et al. Miliary tuberculo¬sis: epidemiologicaland clinical analysis of large-case series from moderate to low tuberculosis endemic Country. Medicine (Baltimore). 2017; 96(5): e5875. doi: https://pubmed.ncbi.nlm.nih.gov/28151863/ (último acceso jun. 2024). DOI: https://doi.org/10.1097/MD.0000000000005875

Garcia-Gasalla M, Fernández-Baca V, Mir-Viladrich I, Cifuentes-Luna C, Cam¬pins-Roselló A, Payeras-Cifre A, et al. Valor de QuantiFERON-TB Gold Test in Tube en el diagnóstico de tuberculosis pulmonar y extrapulmonar. Enferm Infecc Microbiol Clin. 2010; 28(10): 685–689. doi: http://dx.doi.org/10.1016/j. eimc.2010.01.008 (último acceso jun. 2024). DOI: https://doi.org/10.1016/j.eimc.2010.01.008

Manthri S, Vasireddy NK, Bandaru S, Pathak S. Acquired elliptocytosis as a manifestation of myelodysplastic syndrome associated with deletion of chromosome 20q. Case Rep Hematol. 2018; 2018: 1-3. doi: https://dRi. org/10.1155/2018/6819172 (último acceso jun. 2024). DOI: https://doi.org/10.1155/2018/6819172

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 Nov. 21];9(2):71-4. Available from: https://www.reccmi.com/RECCMI/article/view/996