Acute myeloid leukaemia with myelodysplasia-related features

Orpha code: 86845OMIM code: 601626

Definition

A rare acute myeloid leukemia (AML) characterized by the presence of acute leukemia with at least 20% peripheral blood or bone marrow blasts with morphological features of myelodysplasia, or occurrence in patients with a prior history of a myelodysplastic syndrome (MDS) or myelodysplastic/myeloproliferative neoplasm, with MDS-related cytogenetic abnormalities, in the absence of specific genetic abnormalities characteristic of AML with recurrent genetic abnormalities. Prior cytotoxic or radiation therapy for an unrelated disease must be excluded. The condition occurs mainly in elderly patients and is rare in children. Patients often present with severe pancytopenia. Prognosis is generally poor.

Disease data
Classification

Disease

Synonyms
AML with multilineage dysplasia
AML z dysplazją wieloliniową
AML with myelodysplasia-related features
Acute myeloid leukemia with multilineage dysplasia
ORPHA code
86845
OMIM code
601626
ICD10 code
C92.8
ICD11 code
2A60.1

No additional description.

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