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RUNX1::RUNX1T1 Fusion in Pediatric Acute Myeloid Leukemia: A description of two cases
Philippine Journal of Pathology ; (2): 42-48, 2023.
Artigo em Inglês | WPRIM | ID: wpr-984547
ABSTRACT
@#RUNX1RUNX1T1 is a core-binding factor driving fusion gene which arises from t(8;21)(q22;q22). It is one of the most common chromosomal rearrangements in both pediatric and adult Acute Myeloid Leukemia (AML) with a reported incidence o 15% in children and young adults. There are few case reports documenting RUNX1RUNX1T1 translocation in pediatric AML. Although this is generally associated with a favorable prognosis, we report two (2) cases of de novo pediatric AML in the Philippines harboring a RUNX1RUNX1T1 translocation, one eventually relapsed while the other attained remission but succumbed to sepsis.
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Índice: WPRIM (Pacífico Ocidental) Assunto principal: Sequenciamento de Nucleotídeos em Larga Escala Idioma: Inglês Revista: Philippine Journal of Pathology Ano de publicação: 2023 Tipo de documento: Artigo

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Índice: WPRIM (Pacífico Ocidental) Assunto principal: Sequenciamento de Nucleotídeos em Larga Escala Idioma: Inglês Revista: Philippine Journal of Pathology Ano de publicação: 2023 Tipo de documento: Artigo