Inflammatory Myofibroblastic Tumor of the Lung: An Extremely Rare Condition in Adults
- PMID: 31970041
- PMCID: PMC6970563
- DOI: 10.7759/cureus.6432
Inflammatory Myofibroblastic Tumor of the Lung: An Extremely Rare Condition in Adults
Abstract
Inflammatory myofibroblastic tumors (IMTs) of the lung were first reported in 1939. The most common site of predilection is the lungs of the pediatric population. They are extremely rare in adults, constituting less than 1% of adult lung tumors. They are mesenchymal neoplasms that may arise in the soft tissues of almost every organ. IMTs often arise from excessive inflammatory response, and as the name implies, they are composed of myofibroblastic spindle cells accompanied by an inflammatory infiltrate of plasma cells, lymphocytes, and eosinophils.
Keywords: inflammatory myofibroblastic tumor; inflammatory pseudotumor; lung tumors; pseudotumor.
Copyright © 2019, Al-Obaidi et al.
Conflict of interest statement
The authors have declared that no competing interests exist.
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