A Case of Primary Mediastinal Leiomyosarcoma in Which Long-Term Survival Was Achieved

Ann Thorac Cardiovasc Surg. 2020 Apr 20;26(2):95-99. doi: 10.5761/atcs.cr.18-00041. Epub 2018 Mar 30.

Abstract

Introduction: Primary leiomyosarcomas (LMS) of the mediastinum are extremely rare malignant mesenchymal tumors developing from soft tissues or great vessels. We present a case of a primary leiomyosarcoma of the middle mediastinum in which long-term survival was achieved.

Case report: A 77-year-old man presented to us for examination with an extrapleural sign in his upper mediastinum on chest X-ray. Computed tomography (CT) revealed a well-circumscribed mass in the middle mediastinum. Thoracoscopic resection of the mediastinal tumor and immunohistological findings, which were positive for smooth muscle actin (SMA), HHF-35, vimentin, and desmin confirmed primary leiomyosarcoma. It recurred twice with solid right pulmonary metastases, which were resected. He was followed-up for a total of 9 years and 6 months from the first surgery with no signs of recurrence after his last surgery.

Conclusion: Surgical resection of both the primary tumor and pulmonary metastases remains the mainstay of treatment of primary leiomyosarcomas.

Keywords: leiomyosarcoma; mediastinal tumor; pulmonary metastasis.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Humans
  • Leiomyosarcoma / diagnostic imaging
  • Leiomyosarcoma / secondary
  • Leiomyosarcoma / surgery*
  • Lung Neoplasms / diagnostic imaging
  • Lung Neoplasms / secondary
  • Lung Neoplasms / surgery*
  • Male
  • Mediastinal Neoplasms / diagnostic imaging
  • Mediastinal Neoplasms / pathology
  • Mediastinal Neoplasms / surgery*
  • Metastasectomy*
  • Pneumonectomy*
  • Thoracoscopy*
  • Time Factors
  • Treatment Outcome