Literature DB >> 19648793

Sustained engraftment and resolution of bleeding phenotype after unrelated cord blood hematopoietic stem cell transplantation for severe glanzmann thrombasthenia.

Weston Miller1, Amy Dunn, Kuang-Yueh Chiang.   

Abstract

Glanzmann thrombasthenia is a rare, autosomal recessive, qualitative platelet disorder resulting from abnormal platelet surface glycoprotein IIb/IIIa. In phenotypically severe cases, medical management is often challenging. Although definitive hemostasis can be achieved with platelet transfusion, alloimmunization and subsequent platelet refractoriness remain a real risk. To date, only hematopoietic stem cell transplantation has been curative; however, suitable donor availability can be a barrier for some patients. We are the first to report the use of umbilical cord blood hematopoietic stem cell transplantation for Glanzmann thrombasthenia.

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Year:  2009        PMID: 19648793     DOI: 10.1097/MPH.0b013e31819b7228

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  3 in total

Review 1.  Glanzmann thrombasthenia: state of the art and future directions.

Authors:  Alan T Nurden; Xavier Pillois; David A Wilcox
Journal:  Semin Thromb Hemost       Date:  2013-08-08       Impact factor: 4.180

2.  Excellent Outcome Following Sibling Peripheral Blood Hematopoietic Stem Cell Transplantation for Glanzmann Thrombasthenia: A Case Report.

Authors:  Jian Hua Li; Shu Wen Sun; Yuan Ai; Xue Yang; Yi Ping Zhu
Journal:  Front Pediatr       Date:  2022-02-07       Impact factor: 3.418

3.  Allogeneic hematopoietic cell transplantation in an adult patient with Glanzmann thrombasthenia.

Authors:  Ana R Cid; Pau Montesinos; Isabel Sánchez-Guiu; Saturnino Haya; Jose I Lorenzo; Jaime Sanz; Federico Moscardo; Nieves Puig; Dolores Planelles; Santiago Bonanad; Guillermo F Sanz; Vicente Vicente; Consuelo González-Manchón; María L Lozano; José Rivera; Miguel A Sanz
Journal:  Clin Case Rep       Date:  2017-10-05
  3 in total

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