Educational Case: Acute myeloid leukemia, myelodysplasia-related.

Acad Pathol · 2026 · PMC12861219 · PMID 41630800

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fairly significantno p-value reported

For instance, AML with mutated NPM1 , a distinct subtype with a defining genetic abnormality, can present with fairly significant multilineage dysplasia yet is not classified as AML-MR due to its specific molecular features and generally more favorable prognosis.

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