Clinical case reveals post-transfusion purpura and alveolar hemorrhage in a 63-year-old woman, indicating serious transfusion complications.
Post‐transfusion purpura (PTP) is a rare, often undiagnosed, complication associated with transfusion. It is caused by alloimmunization against platelet antigens, which leads to severe acute thrombocytopenia after the transfusion of any product containing platelets, such as red blood cells and platelet concentrates. Here, we present a case of post‐transfusion purpura in a 63‐year‐old woman who developed acute postoperative thrombocytopenia 7 days after receiving a blood transfusion following knee replacement surgery. She was admitted to the intensive care unit with evidence of alveolar haemorrhage. This case study discusses the clinical presentation, diagnosis, laboratory tests, differential diagnosis and treatment with therapeutic plasma exchange, followed by intravenous immunoglobulin and corticosteroids.
No takes yet. Share an insight, caveat, or question.
Yamakova et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: