Thoracic Research and Practice
Poster Presentation

Primary Thoracic Wall Leiomyosarcoma: A Case Report

1.

Department of Thoracic Surgery, Gazi University School of Medicine, Ankara, Turkey

2.

Department of Pathology, Gazi University School of Medicine, Ankara, Turkey

Thorac Res Pract 2019; 20: Supplement 308-308
DOI: 10.5152/TurkThoracJ.2019.308
Read: 1171 Downloads: 674 Published: 08 August 2019

Leiomyosarcomas (LMS) are rare malignant tumors that are mesenchymal in origin. leimyosarcomas constitutes 7% of soft tissue sarcomas. LMS is usually found in the retroperitoneum and extremities, in adults aged 50-70 years whereas chest-wall LMS is rare. 58 years old, male patient was evaluated for right-sided thorax wall lump. The computed tomography (CT) scan of chest reveald a right-sided mass 11.5x8.7x12.8 cm in size which was continuous laterally to the 4th-8th rib and cause a minimal defect in the 5th costal cortex, with intrathoracic extension through between the 5th and 6th intercostal space. PET-BT scan didn’t show any extrathoracic spread. 3rd, 4th, 5th, 6th and 7th ribs were resected with wide negative margin. After that, thoracal wall reconstruction was performed by using 3 titanium bars and prolene mesh. Post-op period was unremarkable. The pathology of the patient was reported as leiomyosarcoma,11 cm in diameter with a high mitotic index. Primary Leiomyosarcomas of the chest wall are rare tumors. Currently, the best option for local control of the tumor is surgical resection with wide negative margin.

Files
EISSN 2979-9139