Cytogenetic biclonality in a child with hypocellular primary myelodysplastic syndrome.
Cancer Genet Cytogenet
; 178(1): 70-2, 2007 Oct 01.
Article
em En
| MEDLINE
| ID: mdl-17889712
ABSTRACT
A 13-year-old boy with hypocellular primary myelodysplastic syndrome, classified as refractory cytopenia, underwent umbilical cord blood transplantation. Cytogenetic analysis revealed two rare biclonal chromosomal aberrations, del(17)(p12) and del(11)(q23). Cytogenetic analysis was a valuable tool in diagnosis, in clinical decision-making, and in treatment and follow-up. To our knowledge, this is the first reported case of cytogenetic biclonality involving chromosomes 17 and 11.
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Coleções:
01-internacional
Temas:
Geral
Base de dados:
MEDLINE
Assunto principal:
Síndromes Mielodisplásicas
Tipo de estudo:
Prognostic_studies
Limite:
Adolescent
/
Humans
/
Male
Idioma:
En
Revista:
Cancer Genet Cytogenet
Ano de publicação:
2007
Tipo de documento:
Article
País de afiliação:
Brasil