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Myeloid neoplasm associated with PDGFRB rearrangement

MONDO:0015690

A rare, malignant, neoplastic disease characterized by clonal proliferation of myeloid and/or lymphoid precursors harboring rearrangements in the PDGFRB gene, in the blood, bone marrow and often other tissues as well (spleen, lymph nodes, skin, etc.). It usually presents as chronic myelomonocytic leukemia with eosinophilia, chronic eosinophilic leukemia, atypical chronic myelogenous leukemia, juvenile myelomonocytic leukemia, myelodysplastic syndrome, acute myeloid leukemia or acute lymphoblastic leukemia. Patients usually present with anemia, leukocytosis, monocytosis, eosinophilia and/or splenomegaly, or systemic symptoms, such as fever, sweating and/or weight loss.

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

1836 clinical trials for this condition and its sub-types, 1 tagged with Myeloid neoplasm associated with PDGFRB rearrangement itself.

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