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ider (9) (q10)t (9;22) (q34;q11.2) as Secondary Karyotypic Aberration of Chronic Myelogeous Leukemia / 대한임상병리학회지
Korean Journal of Clinical Pathology ; : 266-270, 1999.
Artigo em Coreano | WPRIM | ID: wpr-195435
ABSTRACT
Although occasional patients with chronic myeloid leukemia (CML) have chromosomal changes other than Philadelphia chromosome early in the disease, in typical cases the 9;22 translocation remains the sole abnormality throughout the disease course in chronic phase. When disease progression occurs, however, 75-80% develop additional chromosome aberrations. These secondary changes sometimes precede the more aggressive manifestations hematologically and clinically and thus may serve as valuable prognostic indicators. ider (9) (q10)t (9;22) (q34;q11.2) is very rare and a recurrent chromosomal abnormality associated with acute lymphoblastic leukemias (ALL) and lymphoblastic crisis of CML. And ider (9) (q10)t (9;22) (q34;q11.2) is a lymphoid-specific rearrangement and the patients with this abnormality are of older age on average. They commonly show pre-B cell lineage immunophenotype and L2 morphology. We report a case of ider (9) (q10)t (9;22) (q34;q11.2) as secondary aberration in a patient with lymphoblastic crisis of CML.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Cromossomo Filadélfia / Leucemia Mielogênica Crônica BCR-ABL Positiva / Leucemia / Crise Blástica / Aberrações Cromossômicas / Progressão da Doença / Células Precursoras de Linfócitos B / Leucemia-Linfoma Linfoblástico de Células Precursoras Limite: Humanos Idioma: Coreano Revista: Korean Journal of Clinical Pathology Ano de publicação: 1999 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Cromossomo Filadélfia / Leucemia Mielogênica Crônica BCR-ABL Positiva / Leucemia / Crise Blástica / Aberrações Cromossômicas / Progressão da Doença / Células Precursoras de Linfócitos B / Leucemia-Linfoma Linfoblástico de Células Precursoras Limite: Humanos Idioma: Coreano Revista: Korean Journal of Clinical Pathology Ano de publicação: 1999 Tipo de documento: Artigo