Case study demonstrates diagnosis of common variable immunodeficiency in an adult with history of tuberculosis, indicating need for timely intervention.
Common variable immunodeficiency (CVID) is a rare immunodeficiency syndrome presenting with wide manifestations and leading to a delayed diagnosis. A 40-year-old male, a case of old treated tuberculosis, presented with a productive cough and hemoptysis. He had a history of recurrent respiratory symptoms previously attributed to post-tuberculosis sequelae with bilateral bronchiectasis, which can also occur as a manifestation of underlying common variable immunodeficiency (CVID). After a detailed evaluation, serum immunoglobulin levels were markedly reduced, confirming CVID. The patient was started on intravenous immunoglobulin (IVIG) therapy every month. After a six-month follow-up, the patient was symptomatically better and had reduced hospitalizations.
No takes yet. Share an insight, caveat, or question.
Asaithambi et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: