Acute myeloid leukemia with translocations involving the <i>KMT2A</i> gene in twins as a model for the study of leukemogenesis: clinical case reports and genetic characteristics

Familial cases of acute leukemia in children are very rare and are mainly reported in cases of genetically determined predisposition syndromes (mutations in the RUNX1, ETV6, ANKRD26, GATA2, SAMD9/SAMD9L, CEBPA genes) which have been well characterized in the last 15 years. In twins, leukemia is even more rare and is of particular interest for the study of leukemogenesis patterns and evolution of leukemic subclones. Here, we report about three pairs of twins: in one pair, KMT2A-r-leukemia was diagnosed simultaneously, while in the other two cases the second child remained healthy despite the development of KMT2A-r-leukemia in their twin. The patients’ parents gave consent to the use of their children's data, including photographs, for research purposes and in publications.

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Publication Details

Journal
Pediatric Hematology/Oncology and Immunopathology
Published
2025-03-28
DOI
https://doi.org/10.24287/1726-1708-2025-24-1-167-174
Primary Topic
Acute Myeloid Leukemia Research
Type
article
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article

Acute myeloid leukemia with translocations involving the KMT2A gene in twins as a model for the study of leukemogenesis: clinical case reports and genetic characteristics

А. Н. Казакова, Alexander M. Popov, Alexey Maschan, I. Ya. Tomilin et al.
Pediatric Hematology/Oncology and Immunopathology
Acute Myeloid Leukemia Research
article

Acute myeloid leukemia with translocations involving the KMT2A gene in twins as a model for the study of leukemogenesis: clinical case reports and genetic characteristics

А. Н. Казакова, Alexander M. Popov, Alexey Maschan, I. Ya. Tomilin, S. A. Kashpor, М. В. Натрусова, Olga Soldatkina, Г. О. Бронин, У. Н. Петрова, T. V. Konyukhova, D. D. Baydildina, M. V. Gaskova, Yulia Olshanskaya, D. А. Venyov, K. S. Antonova, Elena Zerkalenkova, M. Е. Dubrovina, Dmitry Balashov, С. А. Лебедева, Z. Z. Askerova
article en

Abstract

Familial cases of acute leukemia in children are very rare and are mainly reported in cases of genetically determined predisposition syndromes (mutations in the RUNX1, ETV6, ANKRD26, GATA2, SAMD9/SAMD9L, CEBPA genes) which have been well characterized in the last 15 years. In twins, leukemia is even more rare and is of particular interest for the study of leukemogenesis patterns and evolution of leukemic subclones. Here, we report about three pairs of twins: in one pair, KMT2A-r-leukemia was diagnosed simultaneously, while in the other two cases the second child remained healthy despite the development of KMT2A-r-leukemia in their twin. The patients’ parents gave consent to the use of their children's data, including photographs, for research purposes and in publications.

Pediatric Hematology/Oncology and ImmunopathologyVol. 24(1)
Russian Children's Clinical Hospital (RU), Dmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology (RU)
Openalex Percentile: Top 79%
Acute Myeloid Leukemia Research
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