自体骨髓移植后微血管病性溶血性贫血和肾功能损害：溶血尿毒综合征病例？
Microangiopathic hemolytic anemia and renal impairment following autologous bone marrow transplantation: a case of hemolytic uremic syndrome?
作者信息
Wassmann B, Martin H, Elsner S, Bruecher J, Thaiss F, Stahl R A, Hoelzer D
机构信息
Department of Hematology, Johann Wolfgang Goethe-University, Frankfurt/Main, Germany.
出版信息
Bone Marrow Transplant. 1994 Nov;14(5):849-51.
Thrombotic microangiopathy, which encompasses both thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS), is a severe and life-threatening complication following bone marrow transplantation (BMT). It has been reported after allogeneic BMT but may also occur after autologous BMT. Here we describe a case of microangiopathic hemolytic anemia and progressive renal failure subsequent to autologous BMT.
血栓性微血管病，包括血栓性血小板减少性紫癜（TTP）和溶血尿毒综合征（HUS），是骨髓移植（BMT）后一种严重且危及生命的并发症。它在异基因BMT后已有报道，但也可能发生在自体BMT后。在此，我们描述一例自体BMT后发生微血管病性溶血性贫血和进行性肾衰竭的病例。
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