| Literature DB >> 20503065 |
Raman Verma1, Shawn Malone, Christina Canil, Gerard Jansen, Howard Lesiuk.
Abstract
Primary intra-cranial germ-cell tumours (GCT) are rare and it is important to differentiate them histologically as their prognosis and treatment is quite different. Moreover, highly malignant non-germinomatous GCT (NG GCT) comprise a small portion of these tumours with limited data available on appropriate treatment approaches. We present the case of a 22-year-old male with a unique primary skull-based yolk-sac subtype NG GCT with a literature review of current treatment options. To our knowledge, there have not been any previously published reports of a primary yolk-sac tumour arising from the petrous apex.Entities:
Mesh:
Year: 2010 PMID: 20503065 DOI: 10.1007/s11060-010-0215-8
Source DB: PubMed Journal: J Neurooncol ISSN: 0167-594X Impact factor: 4.130