A CASE OF DELAYED ERYTHROPOIESIS AFTER BONE MARROW TRANSPLANTATION FROM AN ABO-COMPATIBLE SIBLING DONOR FOR ACQUIRED CHRONIC PURE RED CELL APLASIA
Author:
Affiliation:
1. Department of Hematology and Oncology, Nagoya University Graduate School of Medicine
2. Clinical Research Center, National Hospital Organization Nagoya Medical Center
Publisher
Japan Society of Transfusion Medicine and Cell Therapy
Subject
Computer Networks and Communications,Hardware and Architecture,Software
Link
https://www.jstage.jst.go.jp/article/jjtc/63/4/63_614/_pdf
Reference9 articles.
1. 1) Sawada K, Fujishima N, Hirokawa M: Acquired pure red cell aplasia: updated review of treatment. Br J Haematol, 142: 505-514, 2008.
2. 2) Hirokawa M, Sawada K, Fujishima N, et al: Long-term outcome of patients with acquired chronic pure red cell aplasia (PRCA) following immunosuppressive therapy: a final report of the nationwide cohort study in 2004/2006 by the Japan PRCA collaborative study group. Br J Haematol, 169: 879-886, 2015.
3. 3) Musso M, Porretto F, Crescimanno A, et al: Donor lymphocyte infusions for refractory pure red cell aplasia relapsing after both autologous and nonmyeloablative allogeneic peripheral stem cell transplantation. Bone Marrow Transplant, 33: 769-771, 2004.
4. 4) Tseng SB, Lin SF, Chang CS, et al: Successful treatment of acquired pure red cell aplasia (PRCA) by allogeneic peripheral blood stem cell transplantation. Am J Hematol, 74: 273-275, 2003.
5. 5) Müller BU, Tichelli A, Passweg JR, et al: Successful treatment of refractory acquired pure red cell aplasia (PRCA) by allogeneic bone marrow transplantation. Bone Marrow Transplant, 23: 1205-1207, 1999.
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