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Journals / Türk Onkoloji Dergisi / 2019 / Cilt: 34 - Sayı: 4

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

Ömer ÖZBUDAK
Hülya DİROL
Pages
302–306
Publication Date
2022-11-04
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Here in, we report a pulmonary IMT case with clinical,radiological, histopathological features, and 2 year follow up results after complete surgical resection.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Inflammatory myofibroblastic tumor (IMT) is a mesenchymal neoplasm.
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Key Findings & Data:So in any organ, IMT hasthe potential of development.
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Conclusion & Impact:Here in, we report a pulmonary IMT case with clinical,radiological, histopathological features, and 2 year follow up results after complete surgical resection.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

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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Cite This Article

ÖZBUDAK, Ö., DİROL, H. (2022). A case of Pulmonary Inflammatory Fibroblastic Tumor with Clinical, Radiological, Histopathological Features and 2-year follow-up Results and Review of the Literature. Türk Onkoloji Dergisi, Cilt: 34 - Sayı: 4, 302–306. https://ajindex.com/articles/655157

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