| Literature DB >> 21277480 |
J-M Perotin1, G Deslee, D Perdu, V Cahn, P Validire, S Rubin, P Magdeleinat, O Toubas, F Lebargy.
Abstract
Mediastinal liposarcomas (LPS) are rare tumours. We report a case of primary myxoid LPS in a 22-year-old woman suffering from cough, dyspnoea on exercise and asthenia for 3 weeks. Thoracic MRI showed a large tumour on the right side. After neoadjuvant chemotherapy, a complete resection was performed, followed by adjuvant thoracic irradiation. Eighteen months after the diagnosis, no sign of recurrence was detected. Mediastinal LPS include a heterogeneous group of bulky tumours, the progression of which depends on the histological type. The prognosis is dominated by the operability of the tumour. Adjuvant therapies are not established.Entities:
Mesh:
Year: 2011 PMID: 21277480 DOI: 10.1016/j.rmr.2010.05.019
Source DB: PubMed Journal: Rev Mal Respir ISSN: 0761-8425 Impact factor: 0.622