Tetrasomy 8 in a patient with chronic lymphocytic leukemia
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2010
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Resumo |
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. (C) 2010 Elsevier Inc. All rights reserved. FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo)[07/52462-7] National Institute of Science and Technology in Stem Cell and Cell Therapy, Ribeirao Preto, Brazil |
Identificador |
CANCER GENETICS AND CYTOGENETICS, v.198, n.2, p.166-169, 2010 0165-4608 http://producao.usp.br/handle/BDPI/24854 10.1016/j.cancergencyto.2009.12.016 |
Idioma(s) |
eng |
Publicador |
ELSEVIER SCIENCE INC |
Relação |
Cancer Genetics and Cytogenetics |
Direitos |
restrictedAccess Copyright ELSEVIER SCIENCE INC |
Palavras-Chave | #ACUTE MONOBLASTIC LEUKEMIA #TRISOMY-8 #SUBGROUPS #DISEASE #Oncology #Genetics & Heredity |
Tipo |
article original article publishedVersion |