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Monitoring of minimal residual disease and mixed chimerism in a case of high-risk TEL/AML1-positive acute lymphocytic leukemia

Publikace na Ústřední knihovna, 2. lékařská fakulta |
2000

Tento text není v aktuálním jazyce dostupný. Zobrazuje se verze "en".Abstrakt

We report the case of a child with acute lymphocytic leukemia with a combination of positive (TEL/AML1 positivity, age, low level minimal residual disease before bone marrow transplantation) and negative (poor prednisone response, high leukocytosis) prognostic features. We used molecular-genetic techniques and flow cytometry for the follow-up of minimal residual disease.