A complex t(3;8;17) involving breakpoint 8p11 in a case of M5 acute nonlymphocytic leukemia with erythrophagocytosis.
Cancer Genet Cytogenet
; 42(1): 67-73, 1989 Oct 01.
Article
em En
| MEDLINE
| ID: mdl-2790748
The t(8;16)(p11;p13) is a recently described new chromosome rearrangement of acute nonlymphocytic leukemia (ANLL). It appears to be specifically associated with acute monoblastic (AML-M5) or unusual myelomonocytic leukemia with prominent erythrophagocytosis in the leukemic cells. A complex t(3;8;17)(q27;p11;q12) is reported in a case of acute monoblastic leukemia with erythrophagocytosis. Sixteen cases of this t(8;16) and two other variant translocations are reviewed. The pathogenetic mechanism of the variant translocations is discussed, suggesting that the der(8) is a consistent recombinant.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Fagocitose
/
Translocação Genética
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Cromossomos Humanos Par 3
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Cromossomos Humanos Par 8
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Cromossomos Humanos Par 17
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Leucemia Monocítica Aguda
Limite:
Female
/
Humans
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Middle aged
Idioma:
En
Ano de publicação:
1989
Tipo de documento:
Article