Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2019 Dec 20;11(12):e6432.
doi: 10.7759/cureus.6432.

Inflammatory Myofibroblastic Tumor of the Lung: An Extremely Rare Condition in Adults

Affiliations
Case Reports

Inflammatory Myofibroblastic Tumor of the Lung: An Extremely Rare Condition in Adults

Ammar Al-Obaidi et al. Cureus. .

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.

PubMed Disclaimer

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. CT scan of the chest with contrast
1.3 cm opacity in the right upper lobe (A); 2.3 cm nodule in the right lower lobe and 1.4 cm nodule in the left lower lobe (B) Several additional pulmonary nodules are identified within the left lower lobe and lingula; no significant pleural effusion; no pneumothorax; scattered vascular calcifications
Figure 2
Figure 2. CT/PET scan
A hypermetabolic nodule in the right lower lobe CT/PET: positron emission tomography-computed tomography
Figure 3
Figure 3. The pathology specimen demonstrates the characteristic features, including spindle-shaped cells with a high nucleocytoplasmic ratio, pleomorphic hyperchromatic nuclei, brisk mitosis without atypia and intense inflammatory cell infiltrate, especially plasma cells
Morphology of IMT demonstrated (H&E stain A: 100X magnification and B: 400X magnification), (Immunohistochemical staining C: Kappa 400X magnification and D: Lambda 400X magnification) IMT: inflammatory myofibroblastic tumors; H&E: hematoxylin and eosin

References

    1. Inflammatory myofibroblastic lung tumor transforming into intracranial desmoplastic noninfantile ganglioglioma: a case report and literature review. Wei F, Richard SA, Tan J, et al. Medicine (Baltimore) 2018;97:0. - PMC - PubMed
    1. Clinical and histopathologic correlates and management strategies for inflammatory myofibroblastic tumor of the lung. A case series and review of the literature. Sagar AES, Jimenez CA, Shannon VR. Med Oncol, 35. 2018;102:102. - PubMed
    1. Inflammatory myofibroblastic lung tumor: its birth, its bleeding growth, its difficult diagnosis and its surgical end in a child. Pecoraro L, Clemente M, Tadiotto E, Piacentini G, Pietrobelli A, Degani D. Clin Case Rep. 2018;6:1445–1447. - PMC - PubMed
    1. An unusual cause of haemoptysis in a young male. Barbetakis N, Efstathiou A, Xenikakis T, Konstantinidis H, Fessatidis I. Int Semin Surg Oncol. 2006;3:6. - PMC - PubMed
    1. Inflammatory myofibroblastic tumours: where are we now? Gleason BC, Hornick JL. J Clin Pathol. 2008;61:428–437. - PubMed

Publication types

LinkOut - more resources