De Paepe L, Abs R, Verlooy J, Clemens A, Smets R M, Louis P, Martin J J
Department of Endocrinology, University of Antwerp, Belgium.
J Neurol Sci. 1993 Feb;114(2):152-5. doi: 10.1016/0022-510x(93)90290-f.
A male patient is reported with benign intracranial hypertension, who presented with three periods of partial pituitary deficiency, corresponding to episodes of headaches and papilledema. No radiological signs of the empty sella syndrome were observed. Since benign intracranial hypertension has been implicated in the development of the empty sella syndrome, it is postulated that the endocrine deficiency syndrome encountered in the empty sella syndrome can be provoked by chronic intracranial hypertension in itself and is not necessarily secondary to the anatomical changes occurring in the sellar region.
报告了一名患有良性颅内高压的男性患者,该患者出现了三个阶段的部分垂体功能减退,与头痛和视乳头水肿发作相对应。未观察到空蝶鞍综合征的放射学征象。由于良性颅内高压与空蝶鞍综合征的发生有关,因此推测空蝶鞍综合征中出现的内分泌缺乏综合征可能由慢性颅内高压本身引起,不一定继发于蝶鞍区发生的解剖学改变。