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Karyotype analysis of 283 cases of myelodysplastic syndrome / 浙江大学学报·医学版
Journal of Zhejiang University. Medical sciences ; (6): 143-146, 2006.
Article Dans Chinois | WPRIM | ID: wpr-332183
ABSTRACT
<p><b>OBJECTIVE</b>To explore the implication of karyotype analysis in diagnosis and prognosis of myelodysplastic syndrome (MDS).</p><p><b>METHODS</b>The chromosomes were prepared with direct method, brief culture of cells and R-banding techniques, and then the karyotypic analysis was performed.</p><p><b>RESULT</b>Seventy-seven out of 283 patients (27.21%) had karyotypic abnormalities, including the numeral abnormalities of chromosomes and structural alterations. The most common chromosomal aberrations were +8, -20/20q-, -Y, translocation, -7/7q-, +9, -5/5q-. The rate of abnormal karyotype in refractory anemia with erythroblasts (RAEB) and refractory anemia erythroblasts-transformation (RAEB-t) was much higher than in refractory anemia (RA). Patients with abnormal karyotype or higher IPSS scores had a higher risk of transformation into acute leukemia than patients with normal karyotype or lower IPSS scores (P<0.05).</p><p><b>CONCLUSION</b>MDS is a highly heterogenous disorder and karyotype analysis is helpful for its diagnosis and prognosis estimation.</p>
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Pronostic / Translocation génétique / Syndromes myélodysplasiques / Chromosomes humains de la paire 8 / Aberrations des chromosomes / Délétion de segment de chromosome / Génétique / Caryotypage Type d'étude: Étude pronostique Limites du sujet: Adolescent / Adulte / Adulte très âgé / Aged80 / Enfant / Enfant d'âge préscolaire / Femelle / Humains / Mâle langue: Chinois Texte intégral: Journal of Zhejiang University. Medical sciences Année: 2006 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Pronostic / Translocation génétique / Syndromes myélodysplasiques / Chromosomes humains de la paire 8 / Aberrations des chromosomes / Délétion de segment de chromosome / Génétique / Caryotypage Type d'étude: Étude pronostique Limites du sujet: Adolescent / Adulte / Adulte très âgé / Aged80 / Enfant / Enfant d'âge préscolaire / Femelle / Humains / Mâle langue: Chinois Texte intégral: Journal of Zhejiang University. Medical sciences Année: 2006 Type: Article