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Tetrasomy 8 in a patient with chronic lymphocytic leukemia.
de Oliveira, Fábio Morato; Brandão, Renata Amorim; Leite-Cueva, Sabrina Dias; de Paula Careta, Francisco; Simões, Belinda Pinto; Rego, Eduardo Magalhães; Falcão, Roberto Passetto.
Afiliación
  • de Oliveira FM; Department of Internal Medicine, Division of Hematology, School of Medicine of Ribeirão Preto, University of São Paulo, 14049-900 Ribeirão Preto, SP, Brazil. fabiomorato@usp.br
Cancer Genet Cytogenet ; 198(2): 166-9, 2010 Apr 15.
Article en En | MEDLINE | ID: mdl-20362233
We report a case of a 47-year-old man diagnosed with chronic lymphocytic leukemia (CLL) with two extra copies of chromosome 8. Classical cytogenetic analysis by the immunostimulatory combination of DSP30 and interleukin 2 showed tetrasomy of chromosome 8 in 60% of the metaphase cells (48,XY,+8,+8[12]/46,XY[8]). Spectral karyotype analysis confirmed the abnormality previously seen by G banding. Additionally, interphase fluorescence in situ hybridization using an LSI CEP 8 probe performed on peripheral blood cells without any stimulant agent showed tetrasomy of chromosome 8 in 54% of analyzed cells (108 of 200). To our knowledge, tetrasomy 8 as the sole chromosomal abnormality in CLL has not been previously described. The prognostic significance of tetrasomy 8 in CLL remains to be elucidated. However, the patient has been followed up in the outpatient hospital since 2004 without any therapeutic intervention and has so far remained stable.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Poliploidía / Cromosomas Humanos Par 8 / Leucemia Linfocítica Crónica de Células B / Aberraciones Cromosómicas Tipo de estudio: Prognostic_studies Límite: Humans / Male / Middle aged Idioma: En Revista: Cancer Genet Cytogenet Año: 2010 Tipo del documento: Article País de afiliación: Brasil

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Poliploidía / Cromosomas Humanos Par 8 / Leucemia Linfocítica Crónica de Células B / Aberraciones Cromosómicas Tipo de estudio: Prognostic_studies Límite: Humans / Male / Middle aged Idioma: En Revista: Cancer Genet Cytogenet Año: 2010 Tipo del documento: Article País de afiliación: Brasil