Warm Autoimmune Hemolytic Anemia Unmasked by Blood Transfusion in a Patient With Prostate Cancer: A Case Report
Jesheen Mann, Sihab Uddin, Rutbah Khairati, Mubshra Tariq, Zill-e- Huma

TL;DR
A prostate cancer patient developed warm autoimmune hemolytic anemia after a blood transfusion, likely due to cancer-related immune dysregulation.
Contribution
Reports a rare case of warm AIHA in a prostate cancer patient without systemic autoimmune disease or lymphoproliferative disorders.
Findings
The patient's anemia was confirmed as warm autoimmune hemolytic anemia via a strongly positive direct antiglobulin test.
Autoimmune serology showed positive ANA and elevated dsDNA but no evidence of systemic lupus erythematosus or monoclonal proteins.
The patient responded to high-dose prednisolone without further transfusions, suggesting malignancy-associated immune dysregulation as the cause.
Abstract
We report the case of a 65-year-old man with non-metastatic prostate cancer who presented with symptomatic anemia (Hb 66 g/L). With no bleeding source and normal iron studies, anemia of chronic disease was initially suspected. Following transfusion of one unit of red blood cells, he developed clinical and biochemical features of hemolysis. The direct antiglobulin test (DAT) was strongly positive (IgG +4, C3 +3), confirming warm autoimmune hemolytic anemia (AIHA). Further transfusions were administered under steroid cover. Autoimmune serology revealed positive antinuclear antibodies (ANA) and markedly elevated dsDNA by enzyme-linked immunoassay (ELISA) but negative Crithidia assay, indicating low-affinity antibodies and no clinical features suggestive of systemic lupus erythematosus (SLE). No monoclonal proteins were detected, and immunoglobulin profile showed polyclonal…
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Taxonomy
TopicsBlood groups and transfusion · Erythrocyte Function and Pathophysiology · Blood disorders and treatments
