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Myelodysplastic syndrome with hypereosinophilia and a nonrandom chromosomal abnormality dic(1;7): confirmation of eosinophil clonal involvement by fluorescence in situ hybridization.
Forrest, D L; Horsman, D E; Jensen, C L; Berry, B R; Dalal, B I; Barnett, M J; Nantel, S H.
Afiliação
  • Forrest DL; Leukemia/Bone Marrow Transplantation Program of British Columbia, Vancouver General Hospital, Canada.
Cancer Genet Cytogenet ; 107(1): 65-8, 1998 Nov.
Article em En | MEDLINE | ID: mdl-9809037
ABSTRACT
We report a case of de novo myelodysplastic syndrome (MDS) with hypereosinophilia and dic(1;7) in which eosinophil clonal involvement was confirmed by fluorescence in situ hybridization. There have been two previous reports in the literature of eosinophilic MDS with dic(1;7) or t(1;7) in which eosinophil clonality was demonstrated. The specific breakpoints on chromosomes 1 and 7 differ in the three cases, making it difficult to implicate disruption of a single gene as causative; nevertheless, the nonrandom occurrence of t(1;7) or dic(1;7) with malignant eosinophilic proliferations suggests that this chromosomal rearrangement is involved in the etiology of the disease.
Assuntos
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Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomos Humanos Par 1 / Cromossomos Humanos Par 7 / Anemia Refratária / Síndrome Hipereosinofílica Idioma: En Ano de publicação: 1998 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Translocação Genética / Cromossomos Humanos Par 1 / Cromossomos Humanos Par 7 / Anemia Refratária / Síndrome Hipereosinofílica Idioma: En Ano de publicação: 1998 Tipo de documento: Article