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Erythroleukemia Relapsing as Precursor B-cell Lymphoblastic Leukemia / 대한진단검사의학회지
The Korean Journal of Laboratory Medicine ; : 81-85, 2011.
Artigo em Inglês | WPRIM | ID: wpr-152849
ABSTRACT
AML relapsing as ALL has rarely been reported. We describe the case of a 62-yr-old man who was diagnosed with erythroleukemia with a complex karyotype and achieved complete hematologic and cytogenetic remission after induction chemotherapy. However, 4 months after the initial diagnosis, he showed relapse with blasts showing a different morphology and immunophenotype and was diagnosed with precursor B-cell ALL. The relapsing precursor B-cell ALL presented with the same leukemic clones as the primary erythroleukemia. Cytogenetic analysis of his bone marrow (BM) at the time of the primary erythroleukemia showed complex karyotypic abnormalities, including monosomy 5 and monosomy 7. At relapse, his BM showed reemergence of these leukemic clones of complex karyotypic abnormalities with clonal switch. To our knowledge, this is the first case of a lineage switch from erythroleukemia to ALL.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Recidiva / Cromossomos Humanos Par 5 / Cromossomos Humanos Par 7 / Células da Medula Óssea / Leucemia-Linfoma Linfoblástico de Células Precursoras B / Leucemia Eritroblástica Aguda / Transformação Celular Neoplásica / Doença Aguda / Imunofenotipagem / Deleção Cromossômica Limite: Humanos / Masculino Idioma: Inglês Revista: The Korean Journal of Laboratory Medicine Ano de publicação: 2011 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Recidiva / Cromossomos Humanos Par 5 / Cromossomos Humanos Par 7 / Células da Medula Óssea / Leucemia-Linfoma Linfoblástico de Células Precursoras B / Leucemia Eritroblástica Aguda / Transformação Celular Neoplásica / Doença Aguda / Imunofenotipagem / Deleção Cromossômica Limite: Humanos / Masculino Idioma: Inglês Revista: The Korean Journal of Laboratory Medicine Ano de publicação: 2011 Tipo de documento: Artigo