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Two Cases of Possible Familial Chronic Myeloid Leukemia in a Family with Extensive History of Cancer.
Aitken, Marisa J L; Benton, Christopher B; Issa, Ghayas C; Sasaki, Koji; Yilmaz, Musa; Short, Nicholas J.
Afiliação
  • Aitken MJL; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Benton CB; McGovern Medical School, Houston, Texas, USA.
  • Issa GC; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Sasaki K; Rocky Mountain Cancer Center, Denver, Colorado, USA.
  • Yilmaz M; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Short NJ; Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Acta Haematol ; 144(5): 585-590, 2021.
Article em En | MEDLINE | ID: mdl-33735874
CML is defined by the presence of an oncogenic fusion protein caused by a reciprocal translocation between chromosomes 9q and 22q. While our molecular understanding of CML pathogenesis has revolutionized drug development for this disease, we have yet to identify many predisposing factors for CML. Familial occurrence of CML has been rarely reported. Here, we describe 2 cases of CML in a 24-year-old woman and in her 73-year-old maternal great aunt. We describe genetic variants in these patients and report on their environmental exposures that may have contributed to CML pathogenesis. The possible familial association of these 2 cases of CML warrants further investigation into more definitive etiologies of this disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomos Humanos Par 9 / Cromossomos Humanos Par 22 / Síndromes Neoplásicas Hereditárias / Leucemia Mielogênica Crônica BCR-ABL Positiva / Família Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans Idioma: En Revista: Acta Haematol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomos Humanos Par 9 / Cromossomos Humanos Par 22 / Síndromes Neoplásicas Hereditárias / Leucemia Mielogênica Crônica BCR-ABL Positiva / Família Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans Idioma: En Revista: Acta Haematol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos
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