Literature DB >> 1347635

Immune-mediated cytopenia following bone marrow transplantation. Case reports and review of the literature.

T R Klumpp1, C C Block, M A Caligiuri, S N Rabinowe, R J Soiffer, J Ritz.   

Abstract

We describe 3 cases of immune-mediated cytopenia occurring after bone marrow transplantation (BMT). In 1 case, only the platelet line was affected, whereas in the other 2 cases more than 1 cell lineage was involved simultaneously. Two of the cases presented with falling peripheral blood counts following apparently normal early engraftment, while in 1 of the cases the affected lineage failed to appear in the peripheral blood despite normal engraftment of the other lineages. In all 3 cases the cytopenia improved following the initiation of treatment with systemic corticosteroids. Immune-mediated cytopenia following bone marrow transplantation may occur via alloimmune or autoimmune mechanisms. Alloimmune cytopenias have arisen in the context of major or minor mismatches in the ABO system, but cases related to mismatches in the Rh system and other erythroid and non-erythroid alloantigen systems may also occur. Alloimmune cytopenias have been reported primarily in the setting of allogeneic BMT, whereas autoimmune cytopenias have been reported following both allogeneic and autologous BMT. Immune-mediated cytopenia may present as early as the day of transplant, or as late as many months afterward. The possibility of immune-mediated cytopenia should always be considered when unexpected peripheral blood cytopenia is present, or when unexpected hemolysis develops, following bone marrow transplantation. The diagnosis is supported by a normal appearance of the affected lineage or lineages in the bone marrow, the absence of other apparent causes for the cytopenia, and the presence of the relevant auto- or allo-antibodies in the serum. However, any of these features may be absent in individual cases. The importance of these syndromes lies in the fact that they may be life-threatening, yet they often respond well to steroids or other standard immunosuppressive measures. It is important to be aware that effective prophylactic measures are available for patients receiving ABO- or Rh-incompatible marrow.

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Year:  1992        PMID: 1347635     DOI: 10.1097/00005792-199203000-00002

Source DB:  PubMed          Journal:  Medicine (Baltimore)        ISSN: 0025-7974            Impact factor:   1.889


  4 in total

1.  Gelatinous degeneration in a recipient of allogeneic bone marrow transplantation.

Authors:  Yoshinobu Aisa; Takehiko Mori; Tomonori Nakazato; Rie Yamazaki; Yasuo Ikeda; Shinichiro Okamoto
Journal:  Int J Hematol       Date:  2006-12       Impact factor: 2.490

2.  Severe autoimmune thrombocytopenia after allogeneic bone marrow transplantation for aplastic anemia.

Authors:  A Tomonari; A Tojo; T Lseki; J Ooi; H Nagayama; K Ogami; T Maekawa; N Shirafuji; K Tani; S Asano
Journal:  Int J Hematol       Date:  2001-08       Impact factor: 2.490

3.  Identification of anti-thrombopoietin receptor antibody in prolonged thrombocytopenia after allogeneic hematopoietic stem cell transplantation treated successfully with eltrombopag.

Authors:  Akihito Fujimi; Yusuke Kamihara; Akari Hashimoto; Yuji Kanisawa; Chisa Nakajima; Naotaka Hayasaka; Shota Yamada; Toshinori Okuda; Shinya Minami; Kaoru Ono; Satoshi Iyama; Junji Kato
Journal:  Int J Hematol       Date:  2015-05-13       Impact factor: 2.490

4.  Safety of recombinant human thrombopoietin in adults after related donor haploidentical haematopoietic stem cell transplantation: a pilot study.

Authors:  Dai-Hong Liu; Xiao-Jun Huang; Kai-Yan Liu; Lan-Ping Xu; Yu-Hong Chen; Yu Wang; Wei Han; Huan Chen
Journal:  Clin Drug Investig       Date:  2011       Impact factor: 2.859

  4 in total

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