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 a rare, but distinctive mesenchymal neoplasm
composed of fascicles of bland myofibroblasts admixed with a prominent inflammatory …

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

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 an uncommon mesenchymal neoplasm with a
variable histologic appearance that may mimic other spindle cell processes, particularly …

Inflammatory myofibroblastic tumor is an intermediate-grade neoplasm with potential for
recurrence and rare metastasis. Rearrangement of the anaplastic lymphoma kinase gene …

Inflammatory myofibroblastic tumor (IMT) is a genetically heterogenous tumor of the viscera
and soft tissues, with multiple molecular features having been demonstrated in this tumor …

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

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