Symptomatic Rathke's Cleft Cyst With Cavernous Sinus Syndrome -Case Report-
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- MIYAJIMA Yoshiteru
- Department of Neurosurgery, Kitasato University School of Medicine
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- OKA Hidehiro
- Department of Neurosurgery, Kitasato University School of Medicine
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- UTSUKI Satoshi
- Department of Neurosurgery, Kitasato University School of Medicine
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- KONDO Koji
- Department of Neurosurgery, Kitasato University School of Medicine
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- SATO Kimitoshi
- Department of Neurosurgery, Kitasato University School of Medicine
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- FUJII Kiyotaka
- Department of Neurosurgery, Kitasato University School of Medicine
書誌事項
- タイトル別名
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- —Case Report—
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説明
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.<br>
収録刊行物
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- Neurologia medico-chirurgica
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Neurologia medico-chirurgica 47 (12), 576-578, 2007
一般社団法人 日本脳神経外科学会
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詳細情報 詳細情報について
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- CRID
- 1390001205052890368
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- NII論文ID
- 110006532336
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- NII書誌ID
- AN00358613
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- ISSN
- 13498029
- 04708105
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- PubMed
- 18159145
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- 本文言語コード
- en
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- データソース種別
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- JaLC
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