Literature DB >> 9257898

Microangiopathy without hemolysis in a patient following allogeneic bone marrow transplantation.

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.

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Year:  1997        PMID: 9257898     DOI: 10.1038/sj.bmt.1700875

Source DB:  PubMed          Journal:  Bone Marrow Transplant        ISSN: 0268-3369            Impact factor:   5.483


  1 in total

1.  Acquired storage-pool disorders occurring late after allogeneic bone marrow transplantation: partial activation of platelets in asymptomatic patients.

Authors:  C Sakashita; H Akiyama; Y Satoh; T Inoue; K Ohashi; S Mori; H Sakamaki; K Hiruma; M Endoh; N Akamatsu; K Tanoue
Journal:  Int J Hematol       Date:  2001-08       Impact factor: 2.490

  1 in total

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