Two Cases of Possible Familial Chronic Myeloid Leukemia in a Family with Extensive History of Cancer.
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.
Palavras-chave
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