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1.
Cancer Genet Cytogenet ; 92(2): 111-5, 1996 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-8976366

RESUMO

Four children with acute lymphocytic leukemia (ALL) and a dic(9;20) are described. All four patients were diagnosed with pre-B-cell All, and the three for whom information was available were CD10+. Age at diagnosis ranged from 23 months to 12 years. All patients achieved remission, with two in continuous remission for 2 years 6 months and 3 years, one patient relapsed, dying 3 years 2 months after diagnosis, and one patient was lost to follow-up. These four patients were initially diagnosed as having a deletion of 9p and loss of one chromosome 20. Re-examination of the karyotypes indicated a possible dic(9;20). The dicentric chromosome was verified using dual-color fluorescence in situ hybridization (FISH) with centromeric probes for chromosomes 9 and 20 on interphase nuclei. Three of the four patients had multiple chromosomal abnormalities in addition to the translocation; one was hypodiploid, one was pseudodiploid, and two were hyperdiploid. This dicentric chromosome was recently described in four adult and nine pediatric patients with ALL [8, 9]. All reported patients had CD10+ pre-B-cell All, and achieved remission, as was the case for our four pediatric dic(9;20) patients. Two of our three patients for whom follow-up is available are in continuous remission as were two adults and five pediatric patients in the previous reports. These studies confirm the dic(9;20) as a recurring abnormality in ALL. Due to the subtle nature of the translocation, FISH is very useful in confirming the chromosomal abnormality.


Assuntos
Linfoma de Burkitt/genética , Aberrações Cromossômicas , Transtornos Cromossômicos , Cromossomos Humanos Par 20 , Cromossomos Humanos Par 9 , Leucemia-Linfoma Linfoblástico de Células Precursoras B/genética , Translocação Genética , Adulto , Medula Óssea/patologia , Linfoma de Burkitt/mortalidade , Linfoma de Burkitt/patologia , Linfoma de Burkitt/terapia , Centrômero/patologia , Criança , Pré-Escolar , Deleção Cromossômica , Mapeamento Cromossômico , Seguimentos , Humanos , Hibridização in Situ Fluorescente , Lactente , Interfase , Cariotipagem , Leucemia-Linfoma Linfoblástico de Células Precursoras B/mortalidade , Leucemia-Linfoma Linfoblástico de Células Precursoras B/patologia , Leucemia-Linfoma Linfoblástico de Células Precursoras B/terapia , Fatores de Tempo
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