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Br J Haematol ; 120(2): 274-6, 2003 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-12542486

RESUMO

Patients with haematological malignancies involving the NUP98 gene have been reported to have an aggressive clinical course and a poor outcome. We report successful treatment of a 15-year-old Japanese boy with acute myelomonocytic leukaemia having t(2;11)(q31;p15) and a novel fusion transcript, NUP98-HOXD11. He achieved complete remission by combined chemotherapy, and underwent unrelated cord blood transplantation 4 months after diagnosis. He is in complete remission 24 months after diagnosis. Monitoring of minimal residual disease (MRD) showed the absence of fusion transcript 12 months after transplantation. This is the first report of monitoring MRD in a patient with haematological malignancy involving NUP98 fusion transcripts.


Assuntos
Rearranjo Gênico , Leucemia Mielomonocítica Aguda/genética , Proteínas de Fusão Oncogênica/genética , Adolescente , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Cromossomos Humanos Par 11 , Cromossomos Humanos Par 2 , Terapia Combinada , Transplante de Células-Tronco de Sangue do Cordão Umbilical , Humanos , Cariotipagem , Leucemia Mielomonocítica Aguda/tratamento farmacológico , Leucemia Mielomonocítica Aguda/cirurgia , Masculino , Neoplasia Residual , Reação em Cadeia da Polimerase Via Transcriptase Reversa
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