Description
Title: lung inflammation-related myofibroblastic tumor
Abstract: IMTs, or inflammatory myofibroblastic tumors, are a subset of inflammatory pseudo-tumors and were first described in the lung in 1939. Myofibroblastic spindle cells make up the distinctive lesions, which are accompanied by an inflammatory infiltrate of eosinophils, lymphocytes, and psoriasis cells. IMTs can be benign, invade nearby structures, transform into cancer, recur, or even metastasize. They may develop as a result of an inherited disorder or as a complication of autoimmune or infectious diseases. Patients could be asymptomatic or show signs of pneumonia, hemoptysis, dyspnea, pleuritic pain, cough, or dyspnea. We examine the pathophysiology, genetics, clinical manifestation, and imaging findings of IMT of the lung in this article. We also go over the different surgical and non-surgical treatment options as well as the outlook for this disease.
Keywords: inflammatory myofibroblastic tumor of the lung (IMT), inflammatory pseudo-tumor (IPT), pulmonary neoplasm, ALK,bronchoscopy
Paper Quality: SCOPUS / Web of Science Level Research Paper
Subject: Advances in Respiratory Medicine
Writer Experience: 20+ Years
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