Myeloid neoplasm associated with PDGFRA rearrangement

MONDO:0015689

A rare, malignant, neoplastic disease characterized by clonal proliferation of myeloid and/or lymphoid precursors harboring rearrangements in the PDGFRA gene, in the blood, bone marrow and often other tissues as well (spleen, lymph nodes, skin, etc.). It usually presents as chronic eosinophilic leukemia or, less commonly, as acute myeloid leukemia or T-lymphoblastic leukemia with eosinophilia. Patients usually present with eosinophilia, anemia, thrombocytopenia, neutrophilia, splenomegaly, lymphadenopathy, fever, sweating and/or weight loss. Tissue infiltration by eosinophils can manifest with skin rash, erythema, cough, neurological alterations, gastrointestinal symptoms or, rarely, endomyocardial fibrosis and restrictive cardiomyopathy.

Also known as: myeloid and lymphoid neoplasms associated with PDGFRA rearrangement, myeloid and lymphoid neoplasms with PDGFRA rearrangement, myeloid/lymphoid neoplasms with PDGFRA rearrangement, myeloid/lymphoid neoplasm associated with PDGFRA rearrangement

1843 clinical trials for this condition and its sub-types, 1 tagged with Myeloid neoplasm associated with PDGFRA rearrangement itself.

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