Inflammatory myofibroblastic tumors (IMTs) are neoplastic mesenchymal proliferations
featuring an inflammatory infiltrate composed primarily of lymphocytes and plasma cells. The …

ALK oncogenic activation mechanisms were characterized in four conventional spindle‐cell
inflammatory myofibroblastic tumours (IMT) and five atypical IMT, each of which had ALK …

Inflammatory myofibroblastic tumor (IMT) is a rare, but distinctive mesenchymal neoplasm
composed of fascicles of bland myofibroblasts admixed with a prominent inflammatory …

Abnormalities of chromosome 2p23 with expression of ALK1 and p80 occur in both
inflammatory myofibroblastic tumor (IMT) and anaplastic large cell lymphoma. This …

Inflammatory myofibroblastic tumors (IMTs) are rare soft tissue tumors occurring primarily in
children and young adults. ALK gene rearrangements have been identified in this neoplasm …

Inflammatory myofibroblastic tumor (IMT) is a relatively rare soft tissue tumor. The reactive
versus neoplastic pathogenesis of this tumor is unresolved. We found clonal chromosome …

Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal proliferation of transformed
myofibroblasts, with a prominent inflammatory cell component, that can mimic other spindle …

Inflammatory myofibroblastic tumor (IMT) is an uncommon mesenchymal neoplasm with a
variable histologic appearance that may mimic other spindle cell processes, particularly …

Inflammatory myofibroblastic tumor (IMT) is a rare childhood neoplasm. The natural history
of this disease is poorly understood. Recently chromosomal rearrangements involving the …

Inflammatory myofibroblastic tumor (IMT) is a neoplasm composed of myofibroblastic spindle
cells and infiltrating inflammatory cells. Cytogenetic analyses have revealed that a subgroup …