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research article

Characterization of myelodysplastic syndromes progressing to acute lymphoblastic leukemia

Martins, Filipe  
•
Kruszewski, Michael
•
Scarpelli, Ilaria
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2021
Annals Of Hematology

Myelodysplastic syndromes (MDS) are a heterogeneous group of diseases, with a variable probability of transformation into acute leukemia, which is, in the vast majority of cases, of myeloid lineage. Nevertheless, rare cases of acute lymphoblastic leukemia in patients with previously diagnosed MDS have been reported. We describe a series of 3 cases of MDS/CMML marked with evolution to acute lymphoblastic leukemia (ALL) and provide a comprehensive review of the 49 cases documented in the literature so far. These sporadic events have only been published as single-case reports or small series to date. Such atypical cases emphasize the possibility of major phenotypic switches arising at the leukemic stem cell (LSC) and/or early progenitor levels, as a consequence of epigenetic and genomic events driving these changes in the bone marrow niche.

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Type
research article
DOI
10.1007/s00277-020-04114-2
Web of Science ID

WOS:000541008100001

Author(s)
Martins, Filipe  
Kruszewski, Michael
Scarpelli, Ilaria
Schoumans, Jacqueline
Spertini, Olivier
Luebbert, Michael
Blum, Sabine
Date Issued

2021

Publisher

SPRINGER

Published in
Annals Of Hematology
Volume

100

Start page

63

End page

78

Subjects

Hematology

•

myelodysplastic syndrome

•

acute lymphoblastic leukemia

•

acute myeloid leukemia

•

phenotype switch

•

leukemic stem cell

•

hematopoietic stem cell

•

early progenitor

•

mixed lineage leukemia

•

mll

•

ktm2a

•

health-organization classification

•

chronic myelomonocytic leukemia

•

refractory-anemia

•

lineage switch

•

sideroblastic anemia

•

scoring system

•

transformation

•

patient

•

heterogeneity

•

5q-syndrome

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LVG  
Available on Infoscience
July 4, 2020
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/169825
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