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Benign Endobronchial Tumors: A Clinicopathologic Review
Joshua E Insler1, Christopher W Seder2, Karina Furlan3
1Rush Medical College of Rush University Medical Center, Rush University Medical Center, Chicago, IL, United States.
Benign endobronchial tumors, though rare, are often diagnosed via endobronchial resection. These well-defined lesions can cause obstructive symptoms, but treatment yields excellent survival outcomes.
Area of Science:
- Pulmonology
- Thoracic Surgery
- Pathology
Background:
- Benign endobronchial tumors are uncommon and challenging to diagnose due to nonspecific symptoms and vague imaging.
- Accurate diagnosis and effective treatment are crucial for managing these rare airway lesions.
Purpose of the Study:
- To review the clinical, radiologic, and pathologic features of benign endobronchial tumors.
- To analyze diagnostic methods and treatment strategies for these tumors.
- To evaluate patient outcomes and survival rates following treatment.
Main Methods:
- Retrospective analysis of 28 patients with biopsy-proven benign endobronchial tumors from 1993-2018.
- Review of clinicopathologic and radiologic data, focusing on treatment modalities and survival.
- Data collection on tumor types, presenting symptoms, imaging findings, and surgical interventions.
Main Results:
- Hamartoma was the most frequent type (37%), followed by lipoma (19%).
- Common symptoms included cough (58%), shortness of breath (44%), and hemoptysis (15%).
- Endobronchial resection was the preferred diagnostic and therapeutic approach, with no reported deaths.
Conclusions:
- Benign endobronchial tumors typically present as well-defined submucosal or pedunculated lesions.
- These tumors can lead to post-obstructive complications, necessitating timely intervention.
- Endobronchial resection is the optimal strategy for diagnosis and treatment, ensuring favorable patient survival.
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