Bone marrow transplant-associated thrombotic microangiopathy without peripheral blood schistocytes: a case report and review of the literature-Reference-Cited by-同舟云学术

Bone marrow transplant-associated thrombotic microangiopathy without peripheral blood schistocytes: a case report and review of the literature

Published:2018-06-22 Issue:1 Volume:7 Page:
ISSN:2162-3619
Container-title:Experimental Hematology & Oncology
language:en
Short-container-title:Exp Hematol Oncol

Author:

Wirtschafter Eric,VanBeek Christine,Linhares Yuliya^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology,Hematology

Link

http://link.springer.com/content/pdf/10.1186/s40164-018-0106-9.pdf

Reference22 articles.

1. Jodele S, Laskin BL, Dandoy CE, et al. A new paradigm: diagnosis and management of HSCT-associated thrombotic microangiopathy as multi-system endothelial injury. Blood Rev. 2015;29(3):191–204.

2. Gavriilaki E, Imus P, Yuan X, et al. Evidence of complement dysregulation in transplant-associated thrombotic microangiopathy. Haematologica. 2016;100:107.

3. Jodele S, Davies SM, Lane A. Diagnostic and risk criteria for HSCT-associated thrombotic microangiopathy: a study in children and young adults. Blood. 2014;124(4):643–53.

4. Ardissino G, Salardi S, Berra S, et al. Acquired complement regulatory gene mutations and hematopoietic stem cell-related thrombotic microangiopathy. Biol Blood Marrow Transplant. 2017;23(9):1580–96.

5. Rosenthal J. Hematopoietic cell transplantation-associated thrombotic microangiopathy: a review of pathophysiology, diagnosis, and treatment. J Blood Med. 2016;2(7):181–6.

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