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Monosomy 20 in childhood acute lymphoblastic leukemia.
Silengo, M; Vassallo, E; Barisone, E; Miniero, R; Madon, E.
Afiliación
  • Silengo M; Clinica Pediatrica III, Università di Torino, Italy.
Cancer Genet Cytogenet ; 59(2): 177-9, 1992 Apr.
Article en En | MEDLINE | ID: mdl-1581883
ABSTRACT
We report two cases of acute lymphoblastic leukemia (ALL) with loss of chromosome 20 as the only karyotypic abnormality detected in the blast cells. The first patient is a 12-year-old boy studied at diagnosis. He represents the only case of monosomy 20 in our series of 90 pediatric ALL successfully karyotyped at diagnosis. In the second patient, monosomy 20 was detected at the second hematologic relapse, 12 years after the initial diagnosis; cytogenetic studies were not performed at disease onset.
Asunto(s)
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 20 / Leucemia-Linfoma Linfoblástico de Células Precursoras / Monosomía Tipo de estudio: Prognostic_studies Límite: Child / Humans / Male Idioma: En Revista: Cancer Genet Cytogenet Año: 1992 Tipo del documento: Article País de afiliación: Italia
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 20 / Leucemia-Linfoma Linfoblástico de Células Precursoras / Monosomía Tipo de estudio: Prognostic_studies Límite: Child / Humans / Male Idioma: En Revista: Cancer Genet Cytogenet Año: 1992 Tipo del documento: Article País de afiliación: Italia