Ultrastructural, cytogenetic, and molecular findings in mast cell leukemia: Case report

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Abstract

We report a de novo aleukemic form of MCL with a complex monosomic karyotype with LOH for multiple chromosomes and TP53 mutation. Additionally, whereas D816V KIT was not found, the c-Kit transmembrane domain p.M541L variant was detected which is the most common SNP of KIT gene in humans with controversial pathogenic role. In these cases, it is crucial to perform a rapid broad molecular study for an accurate diagnosis which could help to initiate targeted therapy.

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Bosch-Vilaseca, A., Monter-Rovira, A., Cisa-Wieczorek, S., Oñate, G., Bussaglia, E., Carricondo, M., … Nomdedéu, J. F. (2019). Ultrastructural, cytogenetic, and molecular findings in mast cell leukemia: Case report. Clinical Case Reports, 7(7), 1395–1398. https://doi.org/10.1002/ccr3.2208

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