Cutaneous Presentation Mimicking Tuberculosis as an Initial Indicator of Hairy Cell Leukemia: A Case Report

Hairy cell leukemia (HCL) is a rare and slow-progressing lymphoid disorder commonly presenting with splenomegaly and cytopenias. The diagnosis can be challenging due to its nonspecific clinical presentation, frequently resembling other diseases. We report the case of a 48-year-old male patient, whose initial diagnostic hypotheses included cutaneous tuberculosis and reactive arthritis, but the diagnosis was confirmed as HCL after further investigation, including flow cytometry. Treatment with purine analogs led to remission and improved the patient's outcome. This case highlights the complexity of diagnosing HCL, particularly in atypical presentations, and emphasizes the importance of a multidisciplinary approach involving clinical, laboratory, and advanced diagnostic techniques. Despite its rarity, HCL should be considered in patients with unexplained cytopenias and splenomegaly.

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Publication Details

Journal
Cureus
Published
2024-12-30
DOI
https://doi.org/10.7759/cureus.76606
Primary Topic
Chronic Lymphocytic Leukemia Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Cutaneous Presentation Mimicking Tuberculosis as an Initial Indicator of Hairy Cell Leukemia: A Case Report

Catarina Ferreira, Ana Rita Marques, Eduardo Macedo
Cureus
Chronic Lymphocytic Leukemia Research
article

Cutaneous Presentation Mimicking Tuberculosis as an Initial Indicator of Hairy Cell Leukemia: A Case Report

Catarina Ferreira, Ana Rita Marques, Eduardo Macedo
article en

Abstract

Hairy cell leukemia (HCL) is a rare and slow-progressing lymphoid disorder commonly presenting with splenomegaly and cytopenias. The diagnosis can be challenging due to its nonspecific clinical presentation, frequently resembling other diseases. We report the case of a 48-year-old male patient, whose initial diagnostic hypotheses included cutaneous tuberculosis and reactive arthritis, but the diagnosis was confirmed as HCL after further investigation, including flow cytometry. Treatment with purine analogs led to remission and improved the patient's outcome. This case highlights the complexity of diagnosing HCL, particularly in atypical presentations, and emphasizes the importance of a multidisciplinary approach involving clinical, laboratory, and advanced diagnostic techniques. Despite its rarity, HCL should be considered in patients with unexplained cytopenias and splenomegaly.

CureusVol. 16(12)
Hospital Braga (PT)
Openalex Percentile: Top 55%
Chronic Lymphocytic Leukemia Research
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