Glien A, Moser O, Göke F, Wilhelm K, Gerstner A O H
Klinik und Poliklinik für Hals-, Nasen-, Ohren-Heilkunde/Kopf- und Halschirurgie, Universitätsklinikum Halle (Saale), Ernst-Grube-Str. 40, 06120, Halle (Saale), Deutschland.
HNO. 2012 Dec;60(12):1086-90. doi: 10.1007/s00106-012-2643-6.
Mesenchymal chondrosarcoma (MSC) is a very rare sarcoma that is highly malignant with frequent local recurrences and distant metastases leading to a very poor long-term outcome. It differs from classical chondrosarcomas in that it occurs more often in children and commonly in extraskeletal locations. Hardly any evidence-based recommendations for treatment exist. We present the case of a 9-year old boy (pre- and intraoperative findings and histopathological details) who was initially admitted with the diagnosis of a jugular paraganglioma and discuss this case in the light of the recent literature.