Rafei Hind, Yunus Raza, Nassereddine Samah
Department of Internal Medicine, The George Washington University.
Cureus. 2017 May 1;9(5):e1207. doi: 10.7759/cureus.1207.
Post-transfusion purpura is a rare transfusion-related complication that often goes undiagnosed. It is due to alloimmunization against platelet antigens which leads to acute profound thrombocytopenia following the transfusion of any platelet-containing product (red blood cells or platelets). It is commonly seen in multiparous women. Here, we report a case of post-transfusion purpura in a 56-year-old multiparous woman who developed acute thrombocytopenia seven days following a packed red blood cell transfusion. We will discuss the clinical presentation, diagnosis, workup and treatment of this rare disease. It is important to recognize this entity separately and to include it in the differential diagnosis of acute thrombocytopenia after a recent blood transfusion. Treatment for this condition consists of intravenous immunoglobulins, corticosteroids or plasmapheresis.
输血后紫癜是一种罕见的与输血相关的并发症,常未被诊断出来。它是由于针对血小板抗原的同种免疫,导致在输注任何含血小板的产品(红细胞或血小板)后出现急性严重血小板减少。常见于经产妇。在此,我们报告一例56岁经产妇发生的输血后紫癜,该患者在输注浓缩红细胞7天后出现急性血小板减少。我们将讨论这种罕见疾病的临床表现、诊断、检查和治疗。单独认识这一实体并将其纳入近期输血后急性血小板减少的鉴别诊断中很重要。这种情况的治疗包括静脉注射免疫球蛋白、皮质类固醇或血浆置换。