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Donor cell-derived leukemia after cord blood transplantation and a review of the literature: differences between cord blood and BM as the transplant source.
Shiozaki, H; Yoshinaga, K; Kondo, T; Imai, Y; Shiseki, M; Mori, N; Teramura, M; Motoji, T.
Afiliação
  • Shiozaki H; Department of Hematology, Tokyo Women's Medical University, Tokyo, Japan.
  • Yoshinaga K; Department of Hematology, Tokyo Women's Medical University, Tokyo, Japan.
  • Kondo T; Department of Hematology, Tokyo Women's Medical University, Tokyo, Japan.
  • Imai Y; Department of Hematology, Tokyo Women's Medical University, Tokyo, Japan.
  • Shiseki M; Department of Hematology, Tokyo Women's Medical University, Tokyo, Japan.
  • Mori N; Department of Hematology, Tokyo Women's Medical University, Tokyo, Japan.
  • Teramura M; Department of Hematology, Tokyo Women's Medical University, Tokyo, Japan.
  • Motoji T; Department of Hematology, Tokyo Women's Medical University, Tokyo, Japan.
Bone Marrow Transplant ; 49(1): 102-9, 2014 Jan.
Article em En | MEDLINE | ID: mdl-24013690
ABSTRACT
Donor cell-derived leukemia (DCL) is a rare complication of SCT. Here, we present a case of DCL following cord blood transplantation (CBT) and review the clinical features of previously reported DCL. To our knowledge, this is the first report comparing clinical characteristics of DCL from the standpoint of the transplant source, with umbilical cord blood and BM. AML and myelodysplastic syndrome (MDS) were recognized more frequently in DCL after CBT, whereas the incidence of AML and ALL was similar after BMT. The median duration between the occurrence of DCL following CBT and BMT was 14.5 and 36 months, respectively. DCL occurred in a significantly shorter period after CBT than after BMT. Abnormal karyotypes involving chromosome 7 were observed in 52.4% of CBT recipients and 17.3% of BMT recipients; this was a statistically significant difference. Particularly, the frequency of monosomy 7 was significantly higher in DCL after CBT than after BMT. The types of abnormal karyotypes in DCL following BMT were similar to those characteristically observed in adult de novo AML and MDS. DCL patients generally have a poor prognosis in both groups. SCT is the best treatment for curing DCL. DCL appears to have different clinical features according to the transplant source.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doadores de Tecidos / Leucemia / Transplante de Medula Óssea / Transplante de Células-Tronco de Sangue do Cordão Umbilical / Anemia Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Bone Marrow Transplant Assunto da revista: TRANSPLANTE Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doadores de Tecidos / Leucemia / Transplante de Medula Óssea / Transplante de Células-Tronco de Sangue do Cordão Umbilical / Anemia Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Bone Marrow Transplant Assunto da revista: TRANSPLANTE Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Japão
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