| Literature DB >> 29607872 |
Yoshihito Iijima1, Hirohiko Akiyama1, Yuki Nakajima1, Hiroyasu Kinoshita1, Tomomi Hirata1.
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.Entities:
Keywords: leiomyosarcoma; mediastinal tumor; pulmonary metastasis
Mesh:
Year: 2018 PMID: 29607872 PMCID: PMC7184031 DOI: 10.5761/atcs.cr.18-00041
Source DB: PubMed Journal: Ann Thorac Cardiovasc Surg ISSN: 1341-1098 Impact factor: 1.520