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Secondary acute promyelocytic leukemia with t(8;21) and t(9;22) at onset and loss of the Philadelphia chromosome at relapse.
Dallorso, S; Sessarego, M; Garré, M L; Haupt, R; Pasino, M; Sansone, R.
Afiliação
  • Dallorso S; Division of Pediatric Hematology/Oncology, G. Gaslini Children's Hospital, Genova, Italy.
Cancer Genet Cytogenet ; 47(1): 41-6, 1990 Jul 01.
Article em En | MEDLINE | ID: mdl-2357686
ABSTRACT
The translocation (8;21) is a typical marker of the M2 subtype of acute nonlymphocytic leukemia, whereas the Philadelphia (Ph) chromosome is predominantly associated with chronic myelogenous leukemia, and seldom with immature acute leukemias, either lymphoblastic or nonlymphoblastic. Furthermore, the association between t(8;21) and a Ph in the same cell is extremely rare. We present a case of secondary acute promyelocytic leukemia with a karyotype 46,XY,t(8;21), t(9;22) at onset. At relapse the patient lost the Ph, while maintaining the t(8;21). This apparently paradoxical pattern of cytogenetic features and evolution is discussed.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomo Filadélfia / Leucemia Promielocítica Aguda / Deleção Cromossômica Limite: Child / Humans / Male Idioma: En Revista: Cancer Genet Cytogenet Ano de publicação: 1990 Tipo de documento: Article País de afiliação: Itália
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomo Filadélfia / Leucemia Promielocítica Aguda / Deleção Cromossômica Limite: Child / Humans / Male Idioma: En Revista: Cancer Genet Cytogenet Ano de publicação: 1990 Tipo de documento: Article País de afiliação: Itália