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Inflammatory myofibroblastic tumor (IMT) is a rare lesion characterized by myofibroblastic proliferation and inflammatory infiltrate, often misdiagnosed as malignancy. Recent studies suggest that IMT may exhibit neoplastic behavior due to recurrences and cytogenetic abnormalities, challenging its classification as purely reactive. The diagnosis relies on histological examination, with treatment typically involving surgical excision and potential adjunct therapies.

Author

Hajar Errahal

Language

EN