| Literature DB >> 18159145 |
Yoshiteru Miyajima1, Hidehiro Oka, Satoshi Utsuki, Koji Kondo, Kimitoshi Sato, Kiyotaka Fujii.
Abstract
An 88-year-old man presented with Rathke's cleft cyst (RCC) manifesting as complete cavernous sinus syndrome. He had no headache, endocrinological symptom, or blood abnormality. Neuroimaging revealed a cystic intrasellar lesion with lateral extension. The patient underwent surgery by a transsphenoidal approach. Histological examination revealed squamous and cuboidal epithelium. The diagnosis was RCC. RCC is rarely symptomatic, but enlargement and compression of the surrounding structures usually causes headache, visual field defects, or symptoms of pituitary dysfunction. The present case shows that RCC may manifest as complete cavernous sinus syndrome.Entities:
Mesh:
Year: 2007 PMID: 18159145 DOI: 10.2176/nmc.47.576
Source DB: PubMed Journal: Neurol Med Chir (Tokyo) ISSN: 0470-8105 Impact factor: 1.742