Mixed-phenotype acute leukemia (original) (raw)

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dbo:abstract Mixed-phenotype acute leukemia (MPAL) is a group of blood cancers (leukemia) which have combined features of myeloid and lymphoid cancers. It is a rare disease, constituting about 2–5% of all leukemia cases. It mostly involve myeloid with either of T lymphocyte or B lymphocyte progenitors, but in rare cases all the three cell lineages. Knowledge on the cause, clinical features and cellular mechanism is poor, making the treatment and management (prognosis) difficult. The name "mixed-phenotype acute leukemia" was adopted by the World Health Organization in 2008 to include leukemias of ambiguous lineage, acute undifferentiated leukemias and natural killer lymphoblastic leukemias. According to WHO criteria, myeloid lineage is characterised by the presence of myeloperoxidase, while B and T lymphoid lineages are indicated by the expression of CD19 and cytoplasmic CD3. (en) La leucemia a fenotipo misto o a linee miste è una condizione di leucemia acuta dove sono presenti cellule tumorali sia della linea mieloide (leucemia mieloide acuta) che della linea linfoide (leucemia linfoblastica acuta). La definizione clinica raggruppa i vari quadri di leucemia con lineage ambiguo, leucemie acute indifferenziate e leucemie acute linfoblastiche natural-killer. L'origine mieloide è confermata dalla presenza delle mieloperossidasi nelle cellule proliferanti. (it)
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rdfs:comment La leucemia a fenotipo misto o a linee miste è una condizione di leucemia acuta dove sono presenti cellule tumorali sia della linea mieloide (leucemia mieloide acuta) che della linea linfoide (leucemia linfoblastica acuta). La definizione clinica raggruppa i vari quadri di leucemia con lineage ambiguo, leucemie acute indifferenziate e leucemie acute linfoblastiche natural-killer. L'origine mieloide è confermata dalla presenza delle mieloperossidasi nelle cellule proliferanti. (it) Mixed-phenotype acute leukemia (MPAL) is a group of blood cancers (leukemia) which have combined features of myeloid and lymphoid cancers. It is a rare disease, constituting about 2–5% of all leukemia cases. It mostly involve myeloid with either of T lymphocyte or B lymphocyte progenitors, but in rare cases all the three cell lineages. Knowledge on the cause, clinical features and cellular mechanism is poor, making the treatment and management (prognosis) difficult. (en)
rdfs:label Leucemia a lineage ambiguo (it) Mixed-phenotype acute leukemia (en)
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