| Literature DB >> 9257898 |
H Akiyama1, H Yoshinaga, M Endou, S Tanikawa, H Sakamaki, K Tanoue, Y Onozawa.
Abstract
Thrombotic microangiopathy (TMA) is one of the complications of bone marrow transplantation (BMT) which includes hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP). Red cell fragmentation is the most consistent laboratory finding. We present a case of TMA with endothelial damage but without the signs of hemolysis. The patient was not receiving cyclosporine. Partial activation of platelets was also observed. This case represents a new form of TMA in transplant recipients.Entities:
Mesh:
Year: 1997 PMID: 9257898 DOI: 10.1038/sj.bmt.1700875
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.483