Tuberculosis presenting as dual immune dysregulation: Evans syndrome and haemophagocytic lymphohistiocytosis.

BMJ Case RepSep 5, 2026 (epub)

Jisha G Panicker, Somesh Thakur, Deependra Kumar Rai et al.

✦ AI-curated · Sources linked

Case in brief

A middle-aged man with no prior health issues presented with a month-long history of fever, dry cough, weight loss, and worsening breathlessness. Initial tests showed declining blood counts and a chest CT revealed ground-glass opacities and a small pneumothorax. He was diagnosed with Evans syndrome and later secondary haemophagocytic lymphohistiocytosis. Ultimately, disseminated tuberculosis was identified as the underlying cause, and the patient recovered with anti-tubercular therapy and steroids.

Diagnostic / clinical pearl

Clinicians should consider disseminated tuberculosis in patients presenting with immune dysregulation syndromes, such as Evans syndrome and HLH, especially when initial treatments fail.

Source

Published in BMJ Case Rep. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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