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原发性空蝶鞍综合征与良性颅内高压

Primary empty sella syndrome and benign intracranial hypertension.

作者信息

Davis S, Tress B, King J

出版信息

Clin Exp Neurol. 1978;15:248-57.

PMID:756018
Abstract

Two patients presenting with headache and radiological features of an enlarged sella turcica were found to have the primary empty sell syndrome. Whilst under observation, 1 patient developed papilloedema and was shown to have benign intracranial hypertension. The second patient also had raised intracranial pressure. A relationship between the empty sella syndrome and benign intracranial hypertension has previously been reported and it is suggested that in a patient with a congenitally incompetent diaphragma sella, chronically raised intracranial pressure caused herniation of the subarachnoid space into the sella turcica. Subsequently, sella turcica enlargement and remodelling occurs, sometimes with endocrine, visual and other sequelae. The clinical, radiological and CT scan features of the empty sella syndrome are discussed and the indications for major radiological studies are considered.

摘要

两名表现为头痛及蝶鞍增大影像学特征的患者被诊断为原发性空蝶鞍综合征。在观察期间,1例患者出现视乳头水肿,显示患有良性颅内高压。第二例患者也有颅内压升高。此前已有报道空蝶鞍综合征与良性颅内高压之间的关系,提示对于先天性鞍隔缺损的患者,慢性升高的颅内压可导致蛛网膜下腔疝入蝶鞍。随后,蝶鞍增大并重塑,有时会出现内分泌、视觉及其他后遗症。本文讨论了空蝶鞍综合征的临床、影像学及CT扫描特征,并考虑了主要影像学检查的适应证。

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