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About a challenging mediastinal tumor.
Mona Mlika1, Emna Braham2, Rim Hamrouni2
1Department of Pathology, Abderrahman Mami Hospital, Tunis, Tunisia mlika.zorgati.mona@hotmail.com.
Asian Cardiovascular & Thoracic Annals
|June 13, 2015
Summary
Mediastinal hemangiomas are rare tumors. Surgical treatment was successful in 5 patients, with 2 experiencing neurologic symptoms due to neuroforaminal extension.
Area of Science:
- Thoracic surgery
- Vascular tumors
- Diagnostic challenges in oncology
Background:
- Mediastinal hemangiomas represent a rare subset of mediastinal tumors, comprising approximately 0.5% of all cases.
- These vascular tumors present diagnostic difficulties due to nonspecific clinical and radiological findings.
- Neuroforaminal extension is a rare but significant complication.
Purpose of the Study:
- To review a single institution's 10-year experience with mediastinal hemangiomas.
- To highlight the clinical presentation, diagnostic challenges, and surgical outcomes.
- To assess the impact of neuroforaminal extension on patient presentation and management.
Main Methods:
- Retrospective analysis of 5 patients diagnosed with mediastinal hemangiomas over a 10-year period.
- Review of clinical records, radiological imaging, and surgical outcomes.
- Focus on cases with neurologic signs attributed to neuroforaminal extension.
Main Results:
- Five cases of mediastinal hemangiomas were identified and surgically treated.
- Two patients presented with neurologic signs secondary to neuroforaminal extension of the tumor.
- All 5 patients underwent successful surgical resection without postoperative complications.
- Follow-up ranged from 9 months to 2 years, showing no recurrence.
Conclusions:
- Mediastinal hemangiomas, though rare, require surgical intervention.
- Early diagnosis and surgical management are crucial for favorable outcomes.
- Neuroforaminal extension can cause significant neurologic deficits, emphasizing the need for thorough evaluation.

