Opis choroby * EnglishPolish Pobierz sekcję do PDF Definicja 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. Dane Klasyfikacja Choroba Synonimy AML with multilineage dysplasia AML z dysplazją wieloliniową AML with myelodysplasia-related features Acute myeloid leukemia with multilineage dysplasia Kod ORPHA 86845 Kod OMIM 601626 Kod ICD10 C92.8 Kod ICD11 2A60.1 *Źródło Rozszerzony opis choroby Pobierz sekcję do PDF Brak opisu rozszerzonego dla tej choroby. Opracowanie w toku. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl