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Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;10;22)(q34;q22;q11).
Emberger, W; Behmel, A; Tschernigg, M; Seewann, H L; Petek, E; Kroisel, P M; Wagner, K.
Afiliação
  • Emberger W; Institute of Medical Biology and Human Genetics, University of Graz, Harrochgasse 21/8, A-8010 Graz, Austria. werner.emberger@kfunigraz.ac.at
Cancer Genet Cytogenet ; 129(1): 76-9, 2001 Aug.
Article em En | MEDLINE | ID: mdl-11520571
ABSTRACT
We report a 59-year-old, male, chronic myeloid leukemia patient with a rare variant Philadelphia (Ph) translocation t(9;10;22)(q34;q22;q11). Fluorescence in situ hybridization with whole chromosome paints was used to confirm the cytogenetic findings. With a BCR/ABL-specific probe, the known rearrangement on the derivative chromosome 22 was found. The prognostic implications as well as the relevance of the additional breakpoint region 10q22 are discussed.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomos Humanos Par 9 / Cromossomos Humanos Par 10 / Cromossomos Humanos Par 22 / Cromossomo Filadélfia / Leucemia Mielogênica Crônica BCR-ABL Positiva Tipo de estudo: Prognostic_studies Limite: Humans / Male / Middle aged Idioma: En Revista: Cancer Genet Cytogenet Ano de publicação: 2001 Tipo de documento: Article País de afiliação: Áustria
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomos Humanos Par 9 / Cromossomos Humanos Par 10 / Cromossomos Humanos Par 22 / Cromossomo Filadélfia / Leucemia Mielogênica Crônica BCR-ABL Positiva Tipo de estudo: Prognostic_studies Limite: Humans / Male / Middle aged Idioma: En Revista: Cancer Genet Cytogenet Ano de publicação: 2001 Tipo de documento: Article País de afiliação: Áustria