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空蝶鞍综合征合并中枢神经系统囊尾蚴病

Empty sella syndrome associated with central nervous system cysticercosis.

作者信息

Paik K K, Lim S K, Lee H C, Lee E J, Huh K B, Kim D I, Suh J H

出版信息

Korean J Intern Med. 1988 Jul;3(2):128-31. doi: 10.3904/kjim.1988.3.2.128.

Abstract

A 55-year-old woman presented with severe recurrent headache accompanied by dizziness. The brain CT scan showed multiple low-density cystic lesions in the suprasellar and left sylvian cisternae with total empty sell syndrome. The communication between the cisternae and the suprasellar cyst was not verified on the metrizamide CT scan. Treatment with praziquantel resulted in headache inilially and a rise in specific IgG.

摘要

一名55岁女性出现严重复发性头痛并伴有头晕。脑部CT扫描显示鞍上池和左侧外侧裂池有多个低密度囊性病变,伴有完全性空蝶鞍综合征。在甲泛葡胺CT扫描中未证实这些脑池与鞍上囊肿之间存在连通。吡喹酮治疗最初导致头痛,并使特异性IgG升高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/496d/4534961/cd42b6152d55/kjim-3-2-128-6f1.jpg

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本文引用的文献

1
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