A rare presentation of leiomyosarcoma metastasis to the cervical spine: A case report and a brief review

Author:

Koruga Nenad12,Rončević Alen1,Koruga Anamarija Soldo23,Rajc Jasmina24,Flam Josipa25,Rotim Tatjana26,Turk Tajana26,Škiljić Sonja27,Cesarik Marijan8,Paun Tomislav8

Affiliation:

1. Department of Neurosurgery, University Hospital Center Osijek, Osijek, Croatia

2. Faculty of Medicine, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia

3. Department of Neurology, University Hospital Center Osijek, Osijek, Croatia

4. Department of Pathology and Forensic Medicine, University Hospital Center Osijek, Osijek, Croatia

5. Department of Oncology, University Hospital Center Osijek, Osijek, Croatia

6. Department of Diagnostic and Interventional Radiology, University Hospital Center Osijek, Osijek, Croatia

7. Department of Anesthesiology and Critical Care, University Hospital Center Osijek, Osijek, Croatia

8. Department of Neurology, Požega County Hospital, Požega, Požeško-Slavonska, Croatia.

Abstract

Background: Leiomyosarcoma (LMS) is a rare malignancy that originates from smooth muscle. The most common sites of metastases include the lungs, liver, kidney, and skin. Notably, metastases of LMS to the central nervous system/or spine are extremely rare. When a cervical spinal LMS lesion was encountered, the patient successfully underwent gross total tumor resection with negative margins. Case Description: A 63-year-old female had undergone an anterior cervical C5–C7 diskectomy and fusion 18 years ago and resection of a retroperitoneal LMS 3 years ago. She newly presented with right-sided numbness and pain of 2 months duration that correlated with a focal right-sided C5-level hemiparesis (i.e., 4/5 motor strength). When the cervical magnetic resonance demonstrated a right-sided C5 intralaminar mass with extension into the C5–C6 foramen, she underwent posterior tumor resection; pathologically, this proved to be an LMS metastasis. Respectively, 1- and six months postoperatively, follow-up magnetic resonance imaging scans showed no tumor recurrence; she tolerated adjuvant oncological treatment accompanied by physical therapy. However, in one postoperative year, the lesion recurred, and she is presently under consideration for additional surgical management. Conclusion: Gross total surgical resection is the first line of treatment for patients with metastatic LMS. Here, a patient with a C5 laminar/C5–C6 foraminal bony LMS metastasis underwent posterior tumor resection accompanied by adjuvant oncological treatment but exhibited disease recurrence within one postoperative year.

Publisher

Scientific Scholar

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