Myelodysplastic Syndrome: Clinical Characteristics and Significance of Preclinically Detecting Biallelic Mutations in the TET2 Gene

Author:

Danishevich Anastasiia1,Chegodar Anzhelika1ORCID,Bodunova Natalia1,Konovalov Fedor2ORCID,Nefedova Maria2,Kremneva Natalya1,Kurbanov Nizhat1,Bilyalov Airat13ORCID,Nikolaev Sergey1ORCID,Khatkov Igor1,Dudina Galina1

Affiliation:

1. The Loginov Moscow Clinical Scientific Center, 111123 Moscow, Russia

2. Independent Clinical Bioinformatics Laboratory, 123181 Moscow, Russia

3. Institute of Fundamental Medicine and Biology, Kazan Federal University, 420008 Kazan, Russia

Abstract

Myelodysplastic syndrome (MDS) is a clonal disease derived from hematopoietic stem cells, characterized by ineffective hematopoiesis (resulting in peripheral blood cytopenia) and an increased risk of transformation into acute myeloid leukemia. MDS is caused by a complex combination of genetic mutations resulting in a heterogeneous genotype. Genetic studies have identified a set of aberrations that play a central role in the pathogenesis of MDS. In this article, we present a clinical case of MDS transformation into acute myeloid leukemia in the context of two cell lines exhibiting morphological, immunophenotypic, and dysmyelopoiesis markers and the presence of two heterozygous mutations in the TET2 gene.

Funder

Moscow Center for Innovative Technologies in Healthcare

Publisher

MDPI AG

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