A Case of Myxofibrosarcoma in an Unusual Thoracic Location
Document Type
Article
Publication Title
Case reports in oncology
Abstract
Myxofibrosarcoma is a soft tissue neoplasm composed of malignant fibroblasts with a myxoid matrix. It is commonly found in patients during their 6th through 8th decades of life with a slight male predominance. Myxofibrosarcomas are classified as low- to high-grade tumors that are differentiated by hypercellularity, variation of mitotic activity and degree of necrosis. The most common sites are the extremities (77%) and trunk (12%), with the retroperitoneum and mediastinum being very rare. In this case report, we describe a patient presenting with myxofibrosarcoma of the mediastinum, a rare site for the development of myxofibrosarcoma. This case of primary mediastinal myxofibrosarcoma appears to be only the second described in the English-language literature.
First Page
39
Last Page
44
DOI
10.1159/000442875
Publication Date
1-1-2016
Recommended Citation
Gopalratnam, Kavitha; Rodriguez, Jose A.; Woodson, Kevin A.; and Folman, Robert, "A Case of Myxofibrosarcoma in an Unusual Thoracic Location" (2016). Critical Care. 83.
https://scholar.bridgeporthospital.org/critical_care/83
Identifier
26933417 (pubmed); PMC4748782 (pmc); 10.1159/000442875 (doi); cro-0009-0039 (pii)