Ömer ÖZBUDAK, Hülya DİROL

A case of Pulmonary Inflammatory Fibroblastic Tumor with Clinical, Radiological, Histopathological Features and 2-year follow-up Results and Review of the Literature

Inflammatory myofibroblastic tumor (IMT) is a mesenchymal neoplasm. So in any organ, IMT hasthe potential of development. The most common sites that it arises are the lungs. It can occur in anyage, but predominantly in children and adolescents. The etiology is not known. It is poorly understoodon genetic and molecular level either. Clinical symptoms and radiological features are nonspecific inpulmonary IMT, can imitate lung cancer or tuberculosis. Diagnosis is based on histopathologic or immunohistochemical evaluation. The biological behavior is highly unpredictable, rarely metastase, frequently re-occure. Therapeutic approach rely mainly on complete surgical resection although there isno guideline for the treatment or follow-up. Here in, we report a pulmonary IMT case with clinical,radiological, histopathological features, and 2 year follow up results after complete surgical resection.

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