Document Type
Article
Publication Date
2018
Publication Title
Advances in Respiratory Medicine
DOI
10.5603/ARM.2018.0007
Abstract
Inflammatory myofibroblastic tumors (IMT) of the lung, first reported in 1939, are considered a subset of inflammatory pseudo-tumors. They are a distinctive lesions composed of myofibroblastic spindle cells accompanied by an inflammatory infiltrate of plasma cells, lymphocytes, and eosinophils. IMTs may be benign, invade surrounding structures, undergo malignant transformation, recur or may even metastasize. They can occur due to a genetic mutation or can occur secondary to infectious or autoimmune diseases. Patients may be asymptomatic, or present with cough, hemoptysis, dyspnea, pleuritic pain, constitutional symptoms or pneumonia. In this article we review the pathophysiology, genetics, clinical presentation, imaging findings of IMT of the lung. We also discuss the various surgical and non-surgical treatment options and the prognosis associated with this disease.
Recommended Citation
Khatri, A., Agrawal, A., Sikachi, R. R., Mehta, D., Sahni, S., & Meena, N. (2018). Inflammatory Myofibroblastic Tumor of the Lung. Advances in Respiratory Medicine, 86 (1), 27-35. https://doi.org/10.5603/ARM.2018.0007
Publisher's Statement
Originally published in Advances in Respiratory Medicine, 86(1), 27-35. The original material can be found here.
Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 4.0 International License.
