Eight patients with inflammatory myofibroblastic tumor treated with rigid bronchoscopy
- PMID: 39856620
- PMCID: PMC11759437
- DOI: 10.1186/s12890-025-03476-5
Eight patients with inflammatory myofibroblastic tumor treated with rigid bronchoscopy
Abstract
Background: Pulmonary inflammatory myofibroblastic tumor (IMT) accounts for 0.04-0.7% of all lung tumors, and endobronchial IMT accounts for only 10% of all pulmonary IMTs. Little is known about the therapeutic outcomes of rigid bronchoscopy for endobronchial IMT. Here, we report a case series of eight patients with endobronchial IMT underwent rigid bronchoscopy.
Methods: We retrospectively analyzed eight patients with endobronchial IMT between January 2004 and December 2023.
Results: The median age of our patients was 36 years, and 62.5% were male. Dyspnea was the predominant symptom in cases where the tumor was centrally located (n = 6), whereas hemoptysis was the predominant symptom in peripherally located tumors (n = 2). Most cases had high contrast enhancement and a tumor stalk without bronchial wall invasion on computed tomography (CT) and bronchoscopy. Complete endoscopic resection and laser cauterization via rigid bronchoscopy were possible in five patients. There were only two cases in which tumors remained after the procedure, requiring additional treatment (chemotherapy and surgical resection, respectively). In one patient, surgical resection was performed three weeks after the procedure, and the surgical specimen was free of residual tumor. There was no mortality during the median follow-up duration of 18.8 months.
Conclusions: Endoscopic resection and laser cauterization using rigid bronchoscopy may serve as a safe and effective alternative treatment modality to surgery for patients with endobronchial IMT.
Keywords: Endobronchial inflammatory myofibroblastic tumor; Endoscopic resection; Laser cauterization; Rigid bronchoscopy.
© 2025. The Author(s).
Conflict of interest statement
Declarations. Ethics approval and consent to participate: This study was approved by the Institutional Review Board of Samsung Medical Center (IRB no. 2024-04-098). Informed consent was waived by the IRB because it is a retrospective study, many patients are not being followed up, and it does not contain personal information that can be used to infer individual patients. However, we want to emphasize that we strictly adhered to ethical principles and ensured patient confidentiality throughout the study. Consent for publication: Not applicable. Conflict of interest: None of the authors has a financial relationship with a commercial entity that has an interest in the subject of this manuscript. Clinical trial number: Not applicable.
Figures

References
-
- JE G. Idiopathic myositis involving the extraocular muscles. Ophthalmic Rec. 1903;12:471–8.
-
- Brunn H. Two interesting benign lung tumors of contradictory histopathology: remarks on the necessity for maintaining the chest tumor registry. J Thorac Surg. 1939;9(2):119–31.
-
- Siemion K, Reszec-Gielazyn J, Kisluk J, Roszkowiak L, Zak J, Korzynska A. What do we know about inflammatory myofibroblastic tumors? - a systematic review. Adv Med Sci. 2022;67(1):129–38. - PubMed
-
- Pettinato G, Manivel JC, De Rosa N, Dehner LP. Inflammatory myofibroblastic tumor (plasma cell granuloma). Clinicopathologic study of 20 cases with immunohistochemical and ultrastructural observations. Am J Clin Pathol. 1990;94(5):538–46. - PubMed
MeSH terms
LinkOut - more resources
Full Text Sources
Medical