Rathke's cleft cyst with pituitary apoplexy: case report

被引：38

作者：

Nishioka, H ^{[1
]}

Ito, H ^{[1
]}

Miki, T ^{[1
]}

Hashimoto, T ^{[1
]}

Nojima, H ^{[1
]}

Matsumura, H ^{[1
]}

机构：

[1] Tokyo Med Univ, Dept Neurosurg, Shinjuku Ku, Tokyo 1600023, Japan

来源：

NEURORADIOLOGY | 1999年 / 41卷 / 11期

关键词：

pituitary tumor; cyst Rathke's cleft; pituitary apoplexy; magnetic resonance imaging;

D O I：

10.1007/s002340050851

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

We report a Rathke's cleft cyst which presented as pituitary apoplexy, a rare presentation. A 46-year-old woman suffered sudden headache and visual loss. T1-weighted MRI3 weeks after this apoplectic episode demonstrated a cystic lesion between the anterior and posterior lobes of the pituitary, with some high-signal material layering in it, The mass showed spontaneous regression on an image 3 weeks later. Trans-sphenoidal surgery confirmed the diagnosis of a Rathke's cleft cyst with a haematoma within it.

引用

页码：832 / 834

页数：3

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