Population
A 37-year-old woman presenting with shortness of breath and dyspnea, diagnosed with a mediastinal tumor…
Design
Case_report
Follow-up
19 days postoperatively
Authors
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May support surgical feasibility in rare mediastinal sarcomas with SVC syndrome; leaves open need for larger series on outcomes.
This report describes an extremely rare case of low-grade fibromyxoid sarcoma originating in the mediastinum and causing superior vena cava syndrome, which was successfully treated with surgical resection and vascular reconstruction.
Takeda et al. (2000) studied this question.
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