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Robotic Enucleation of Esophageal Leiomyoma
Published on: February 20, 2026
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Rare mediastinal leiomyoma in a child
Zubair Ashraf Hakeem1, Shyam Singh Rathore2, Abdul Wahid2
1Department of Cardiovascular and Thoracic Surgery, Sher-I-Kashmir Institute of Medical Sciences, Soura, Srinagar, Kashmir, India. drhzashraf@yahoo.co.in.
General Thoracic and Cardiovascular Surgery
|September 19, 2016
Summary
Mediastinal leiomyomas, rare tumors arising from smooth muscle, can grow large. This case highlights a huge anterior mediastinal leiomyoma in a child, successfully removed surgically.
Area of Science:
- Thoracic surgery
- Pediatric oncology
- Pathology
Background:
- Mediastinal leiomyomas originate from smooth muscle cells within mediastinal vasculature.
- Typically located in the posterior mediastinum, often associated with the esophagus.
- These tumors are exceptionally rare, particularly in pediatric patients.
Observation:
- A rare case of a massive mediastinal leiomyoma in a 1.5-year-old male child is presented.
- The tumor was situated in the lower anterior mediastinum, causing significant compression.
- Clinical manifestations included cardiac and hepatic compression, and rib cage deformity.
Findings:
- Surgical excision was performed via median sternotomy and a right mini-thoracotomy.
- Histopathological examination confirmed the diagnosis of leiomyoma.
- The tumor's large size and anterior location were notable features.
Implications:
- This case underscores the possibility of large anterior mediastinal leiomyomas in children.
- Highlights the importance of surgical intervention for symptomatic mediastinal masses.
- Contributes to the understanding of rare pediatric thoracic tumors and their management.
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