Tetrasomy 8 in a patient with chronic lymphocytic leukemia


Autoria(s): OLIVEIRA, Fabio Morato de; BRANDAO, Renata Amorim; LEITE-CUEVA, Sabrina Dias; CARETA, Francisco de Paula; SIMOES, Belinda Pinto; REGO, Eduardo Magalhaes; FALCAO, Roberto Passetto
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

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

http://dx.doi.org/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