| Literature DB >> 11003297 |
W A Simoens1, L van den Hauwe, E Van Hedent, F Warson, R Demaeseneer, D Williams, A M De Schepper.
Abstract
We report a case of a primary amyloidoma of the skull base. Plain radiography and CT showed a lytic, highly destructive lesion with multiple scattered calcifications within. MR imaging revealed that the tumor was isoto hypointense to muscle on T1-weighted images and extremely hypointense on T2-weighted images. In contrast to two previous reports, marked enhancement after the administration of contrast material was absent. Bone amyloidomas are very rare and are frequently misinterpreted as chondrosarcomas.Entities:
Mesh:
Year: 2000 PMID: 11003297 PMCID: PMC7974035
Source DB: PubMed Journal: AJNR Am J Neuroradiol ISSN: 0195-6108 Impact factor: 3.825