| Literature DB >> 9285613 |
J C Ouallet1, K Marsot-Dupuch, R Van Effenterre, M Kujas, J M Tubiana.
Abstract
This report describes a patient with von Hippel-Lindau disease who presented with an 8-year history of a slow-growing, locally invasive vascularized lesion of the temporal bone involving the cerebellopontine angle. The mass, studied by computerized tomography scanning and magnetic resonance imaging techniques, was partly cystic in appearance. After removal of the mass, pathological studies confirmed a papillary cystic tumor with characteristics that have been described in tumors with an endolymphatic sac origin. These rare neoplasms constitute a distinct pathological entity and deserve wider recognition.Entities:
Mesh:
Year: 1997 PMID: 9285613 DOI: 10.3171/jns.1997.87.3.0445
Source DB: PubMed Journal: J Neurosurg ISSN: 0022-3085 Impact factor: 5.115