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The Korean Journal of Laboratory Medicine ; : 510-514, 2009.
Artículo en Coreano | WPRIM | ID: wpr-106766

RESUMEN

Tetraploidy or near-tetraploidy is a rare cytogenetic abnormality found in AML, and is divided into primary and secondary forms. The secondary tetraploidy or near-tetraploidy found in AML is known to be specifically associated with t(8;21). In this case report, FISH analysis detected RUNX1-RUNX1T1 gene rearrangement in the absence of cytogenetic abnormality of t(8;21), which suggests the presence of unvailed t(8;21). This is the first case report of tetraploidy or near-tetraploidy AML with cryptic RUNX1/RUNX1T1 in Korea. Although the prognosis of tetraploidy or near- tetraploidy with t(8;21) is known to be poor, this patient shows a relatively good clinical course compared to other reported cases.


Asunto(s)
Adulto , Femenino , Humanos , Cromosomas Humanos Par 21 , Cromosomas Humanos Par 8 , Subunidad alfa 2 del Factor de Unión al Sitio Principal/genética , Reordenamiento Génico , Hibridación Fluorescente in Situ , Cariotipificación , Leucemia Mieloide Aguda/genética , Poliploidía , Proteínas Proto-Oncogénicas/genética , Factores de Transcripción/genética , Translocación Genética
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