Successful allogeneic bone marrow transplantation using immunosuppressive conditioning regimen for a patient with red blood cell transfusion-dependent pyruvate kinase deficiency anemia
Pyruvate kinase deficiency (PKD) is the rare glycolytic enzyme defect causing hemolytic anemia. Treatments are mainly red cell transfusion and/or splenectomy, leading to iron overload. Allogeneic bone marrow transplantation (BMT) is alternatively curative treatment for severe PKD. The intensity of...
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doaj-942b1a82b8864f80b763fa1cbc1c21c92020-11-25T03:54:33ZengPAGEPress PublicationsHematology Reports2038-83222038-83302020-05-0112110.4081/hr.2020.8305Successful allogeneic bone marrow transplantation using immunosuppressive conditioning regimen for a patient with red blood cell transfusion-dependent pyruvate kinase deficiency anemiaMaiko Shimomura0Takehiko Doi1Shiho Nishimura2Yusuke Imanaka3Shuhei Karakawa4Satoshi Okada5Hiroshi Kawaguchi6Masao Kobayashi7Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, HiroshimaDepartment of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, HiroshimaDepartment of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, HiroshimaDepartment of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, HiroshimaDepartment of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, HiroshimaDepartment of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, HiroshimaDepartment of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, HiroshimaDepartment of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences, Hiroshima Pyruvate kinase deficiency (PKD) is the rare glycolytic enzyme defect causing hemolytic anemia. Treatments are mainly red cell transfusion and/or splenectomy, leading to iron overload. Allogeneic bone marrow transplantation (BMT) is alternatively curative treatment for severe PKD. The intensity of conditioning is often controversial because of higher risk of graft failure and organ damage. Here, we present a transfusion-dependent PKD patient undergoing BMT from an HLA-identical sibling using intensively immunosuppressive conditioning regimen. This report suggests that BMT using immunosuppressive conditioning regimen may be a feasible and effective treatment for patients with severe PKD with iron overload. We suggest the timing of the transplantation at an earlier age in severe PKD predicted from gene mutation is preferred before cumulative damage of transfusion. https://www.pagepress.org/journals/index.php/hr/article/view/8305Pyruvate kinase deficiencyallogeneic hematopoietic cell transplantationimmunosuppressive conditioning regimen |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Maiko Shimomura Takehiko Doi Shiho Nishimura Yusuke Imanaka Shuhei Karakawa Satoshi Okada Hiroshi Kawaguchi Masao Kobayashi |
spellingShingle |
Maiko Shimomura Takehiko Doi Shiho Nishimura Yusuke Imanaka Shuhei Karakawa Satoshi Okada Hiroshi Kawaguchi Masao Kobayashi Successful allogeneic bone marrow transplantation using immunosuppressive conditioning regimen for a patient with red blood cell transfusion-dependent pyruvate kinase deficiency anemia Hematology Reports Pyruvate kinase deficiency allogeneic hematopoietic cell transplantation immunosuppressive conditioning regimen |
author_facet |
Maiko Shimomura Takehiko Doi Shiho Nishimura Yusuke Imanaka Shuhei Karakawa Satoshi Okada Hiroshi Kawaguchi Masao Kobayashi |
author_sort |
Maiko Shimomura |
title |
Successful allogeneic bone marrow transplantation using immunosuppressive conditioning regimen for a patient with red blood cell transfusion-dependent pyruvate kinase deficiency anemia |
title_short |
Successful allogeneic bone marrow transplantation using immunosuppressive conditioning regimen for a patient with red blood cell transfusion-dependent pyruvate kinase deficiency anemia |
title_full |
Successful allogeneic bone marrow transplantation using immunosuppressive conditioning regimen for a patient with red blood cell transfusion-dependent pyruvate kinase deficiency anemia |
title_fullStr |
Successful allogeneic bone marrow transplantation using immunosuppressive conditioning regimen for a patient with red blood cell transfusion-dependent pyruvate kinase deficiency anemia |
title_full_unstemmed |
Successful allogeneic bone marrow transplantation using immunosuppressive conditioning regimen for a patient with red blood cell transfusion-dependent pyruvate kinase deficiency anemia |
title_sort |
successful allogeneic bone marrow transplantation using immunosuppressive conditioning regimen for a patient with red blood cell transfusion-dependent pyruvate kinase deficiency anemia |
publisher |
PAGEPress Publications |
series |
Hematology Reports |
issn |
2038-8322 2038-8330 |
publishDate |
2020-05-01 |
description |
Pyruvate kinase deficiency (PKD) is the rare glycolytic enzyme defect causing hemolytic anemia. Treatments are mainly red cell transfusion and/or splenectomy, leading to iron overload. Allogeneic bone marrow transplantation (BMT) is alternatively curative treatment for severe PKD. The intensity of conditioning is often controversial because of higher risk of graft failure and organ damage. Here, we present a transfusion-dependent PKD patient undergoing BMT from an HLA-identical sibling using intensively immunosuppressive conditioning regimen. This report suggests that BMT using immunosuppressive conditioning regimen may be a feasible and effective treatment for patients with severe PKD with iron overload. We suggest the timing of the transplantation at an earlier age in severe PKD predicted from gene mutation is preferred before cumulative damage of transfusion.
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topic |
Pyruvate kinase deficiency allogeneic hematopoietic cell transplantation immunosuppressive conditioning regimen |
url |
https://www.pagepress.org/journals/index.php/hr/article/view/8305 |
work_keys_str_mv |
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