Allogeneic stem cell transplant is a successful treatment for severe aplastic anemia. Subsequent development of acute leukemia is a rare event. Cytogenetic/molecular analysis has shown that leukemia can originate in the host cells. In this report we describe a pediatric patient who developed donor cell acute myeloid leukemia with a del (9q) aberration and a CEBPA double mutation, 11 years after an unrelated allogeneic stem cell transplant for severe acquired aplastic anemia. Mechanisms involved in the pathogenesis are complex and several hypotheses have been proposed. Novel approaches, such as next generation sequencing to unravel the mechanisms of leukemogenesis in this category of patients, appear promising.
DONOR CELL ACUTE MYELOID LEUKEMIA WITH DEL(9q) IN A PEDIATRIC PATIENT OCCURRING 11 YEARS FROM TRANSPLANT FOR SEVERE APLASTIC ANEMIA / Testi, Anna Maria; Kaiser, Francesca; Paola Iori, Anna; Barberi, Walter; LA ROCCA, Ursula; Moleti, MARIA LUISA; Bianchi, Simona; Pigazzi, Martina; Buldini, Barbara; Mancini, Marco; Foà, Robin; Giona, Fiorina. - In: JOURNAL OF HEMATOLOGY & THROMBOEMBOLIC DISEASES. - ISSN 2329-8790. - (2021), pp. 1-4.
DONOR CELL ACUTE MYELOID LEUKEMIA WITH DEL(9q) IN A PEDIATRIC PATIENT OCCURRING 11 YEARS FROM TRANSPLANT FOR SEVERE APLASTIC ANEMIA
Anna Maria Testi;Francesca Kaiser;Walter Barberi;Ursula La Rocca;Maria Luisa Moleti;Robin Foà;Fiorina Giona
2021
Abstract
Allogeneic stem cell transplant is a successful treatment for severe aplastic anemia. Subsequent development of acute leukemia is a rare event. Cytogenetic/molecular analysis has shown that leukemia can originate in the host cells. In this report we describe a pediatric patient who developed donor cell acute myeloid leukemia with a del (9q) aberration and a CEBPA double mutation, 11 years after an unrelated allogeneic stem cell transplant for severe acquired aplastic anemia. Mechanisms involved in the pathogenesis are complex and several hypotheses have been proposed. Novel approaches, such as next generation sequencing to unravel the mechanisms of leukemogenesis in this category of patients, appear promising.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


