| Literature DB >> 20185881 |
Tetsuro Sameshima1, Rokuya Tanikawa, Toshihide Sugimura, Naoto Izumi, Toshitaka Seki, Takahiro Maeda, Toshiyuki Tsuboi, Masaaki Hashimoto, Teruo Kimura, Kazuki Nabeshima.
Abstract
A 51-year-old female presented with a rare case of choroid plexus papilloma originating in the sella turcica manifesting as headaches that was not readily distinguishable preoperatively from pituitary adenoma. Head magnetic resonance imaging revealed a tumor extending from the sella turcica to the suprasellar cistern. The tumor was removed via an endonasal transsphenoidal approach. Histological examination indicated a papillary structure covered with a layer of columnar epithelial cells that resembled normal choroid plexus. These findings, together with immunohistochemistry, led to a diagnosis of choroid plexus papilloma.Entities:
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Year: 2010 PMID: 20185881 DOI: 10.2176/nmc.50.144
Source DB: PubMed Journal: Neurol Med Chir (Tokyo) ISSN: 0470-8105 Impact factor: 1.742