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- W4379375369 abstract "Inflammatory myofibroblastic tumors (IMT) are rare borderline tumors with a variable histological appearance that may mimic multiple mesenchymal tumors. We present a rare case of a challenging abdominal mass discovered in a premature newborn. The histopathology showed a bland myofibroblastic proliferation associated with an inflammatory infiltrate that was positive for smooth muscle actin and desmin but negative for anaplastic lymphoma kinase (ALK) protein. The diagnosis of an ALK-negative IMT was established. The tumor was partially resected. After six months of follow-up, the residual tumor remained stable, and the patient was asymptomatic. The correct diagnosis and subsequent treatment of ALK-negative IMT require appropriate histopathological, immunohistochemical, and sometimes genetic examination. Further research has to be conducted to help clinicians make an appropriate treatment plan." @default.
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- W4379375369 date "2023-06-27" @default.
- W4379375369 modified "2023-09-26" @default.
- W4379375369 title "ALK-Negative Inflammatory Myofibroblastic Tumor: A Challenging Case in a Premature Newborn" @default.
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- W4379375369 doi "https://doi.org/10.3233/npm-230007" @default.
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