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A Case of Pediatric Precursor B-cell Acute Lymphoblastic Leukemia Associated with Translocations (14;18)(q32;q21) and (8;9)(q24;p13) / 임상소아혈액종양
Article em En | WPRIM | ID: wpr-788605
Biblioteca responsável: WPRO
ABSTRACT
Precursor B-cell acute lymphoblastic leukemia (ALL), which is the most common subtype of pediatric acute leukemia, generally has a good prognosis. However, the prognosis also depends on the genetic abnormalities of the leukemic blast. Concurrent MYC and IGH/BCL2 translocations have recently been reported as a “double hit” in adult patients, but non-immunoglobulin (non-IG)/MYC translocation has rarely been reported. In this paper, we report a case of pediatric precursor B-cell ALL associated with translocations (14;18)(q32;q21) and (8;9)(q24;p13). The patient was a previously healthy 13-year-old boy. Complete remission was not achieved after first-line four-drug induction chemotherapy; thus, intensive salvage regimen, including high-dose cytarabine and L-asparaginase, were administered, which resulted in morphologic remission. However, his disease relapsed during the second cycle of salvage regimen, and he died of sepsis-induced multiorgan failure.
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Texto completo: 1 Índice: WPRIM Assunto principal: Prognóstico / Leucemia-Linfoma Linfoblástico de Células Precursoras B / Leucemia / Citarabina / Células Precursoras de Linfócitos B / Leucemia-Linfoma Linfoblástico de Células Precursoras / Quimioterapia de Indução Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Humans / Male Idioma: En Revista: Clinical Pediatric Hematology-Oncology Ano de publicação: 2017 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Prognóstico / Leucemia-Linfoma Linfoblástico de Células Precursoras B / Leucemia / Citarabina / Células Precursoras de Linfócitos B / Leucemia-Linfoma Linfoblástico de Células Precursoras / Quimioterapia de Indução Tipo de estudo: Prognostic_studies Limite: Adolescent / Adult / Humans / Male Idioma: En Revista: Clinical Pediatric Hematology-Oncology Ano de publicação: 2017 Tipo de documento: Article