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Inflammatory Myofibroblastic Tumor

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Soft Tissue Tumors
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Abstract

Inflammatory myofibroblastic tumor is a neoplasm of intermediate biological aggressiveness and is classified among the fibroblastic—myofibroblastic tumors. It is also known as plasma cell granuloma, inflammatory myofibrohistiocytic proliferation, omental mesenteric myxoid hamartoma, inflammatory pseudotumor, inflammatory fibrosarcoma, and inflammatory myofibroblastic sarcoma.

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Notes

  1. 1.

    SMA: smooth muscle actin.

  2. 2.

    MSA: muscle-specific actin.

  3. 3.

    HHV8: human herpesvirus 8.

  4. 4.

    ALK-based fusion gene: ALK (anaplastic lymphoma kinase) encodes a receptor tyrosine kinase, which belongs to the insulin receptor superfamily. It plays an important role in the development of the brain. ALK has been found to be rearranged, mutated, or amplified in a series of tumors including anaplastic large cell lymphomas, neuroblastoma, and non-small cell lung cancer.

  5. 5.

    Crizotinib: small molecule tyrosine kinase inhibitor targeting the following: ALK, MET.

  6. 6.

    Alectinib: small molecule tyrosine kinase inhibitor targeting the following: ALK.

  7. 7.

    Ceritinib: small molecule tyrosine kinase inhibitor targeting the following: ALK.

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Correspondence to Simone Mocellin .

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Mocellin, S. (2021). Inflammatory Myofibroblastic Tumor. In: Soft Tissue Tumors . Springer, Cham. https://doi.org/10.1007/978-3-030-58710-9_133

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  • DOI: https://doi.org/10.1007/978-3-030-58710-9_133

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-030-58709-3

  • Online ISBN: 978-3-030-58710-9

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