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[继发性空蝶鞍综合征:三例报告及文献复习]

[Secondary empty sella syndrome: report of three cases and review of the literature].

作者信息

Keyaki A, Makita Y, Nabeshima S, Motomochi M, Itagaki T, Tei T

出版信息

No Shinkei Geka. 1982 Nov;10(11):1189-94.

PMID:7155293
Abstract

Three cases of the secondary empty sella syndrome were reported. Case 1. A 57-year-old female was admitted to our clinic because of recurrent visual disturbance. Fourteen years previously a pituitary adenoma was diagnosed and two courses of radiation therapy was given elsewhere, the total dosage being unknown. Pneumoencephalography revealed air collection in the sellar cavity. Exploratory craniotomy demonstrated an empty sella with downward migration of the optic nerve and chiasm. Case 2. A 40-year-old female was readmitted to our clinic for possible recurrent pituitary adenoma. Three years previously she underwent transsphenoidal surgery and postoperative radiation therapy with a tumor dose of 6,400 rad. She had headache and visual disturbance. Pneumoencephalography showed air extension into the sellar cavity. Case 3. A 50-year-old female was readmitted to our clinic because of general prostration and headache. Ten years previously she received transsphenoidal surgery and postoperative radiation therapy with a tumor dose of 6,650 rad for a pituitary adenoma. Endocrine evaluation revealed a hypopituitarism. Pneumoencephalography showed air extension into the sellar cavity. The etiology of secondary empty sella has not been clarified yet, although the primary empty sella has been considered to result from incomplete development of the diaphragma sellae. We consider that the most important factor should be present in the diaphragma itself. It is conceivable that the diaphragma sellae becomes weak due to 1) compression by the tumor, 2) mechanical injury during operation, 3) radiation effect. Then, these preceding factors might bring about herniation of the optic nerve and chiasm with the diaphragma sellae into the sellar cavity. Therefore, we propose that early diagnosis of pituitary tumor should be important, and that careful packing of the sellar floor at transsphenoidal surgery should be essential to prevent occurrence of the secondary empty sella syndrome.

摘要

报告了3例继发性空蝶鞍综合征。病例1:一名57岁女性因反复出现视力障碍入院。14年前诊断为垂体腺瘤,在其他地方接受了两个疗程的放射治疗,总剂量不详。气脑造影显示蝶鞍腔内有气体聚集。 exploratory开颅手术显示为空蝶鞍,视神经和视交叉向下移位。病例2:一名40岁女性因可能复发的垂体腺瘤再次入院。3年前她接受了经蝶窦手术和术后放射治疗,肿瘤剂量为6400拉德。她有头痛和视力障碍。气脑造影显示气体延伸至蝶鞍腔。病例3:一名50岁女性因全身乏力和头痛再次入院。10年前她因垂体腺瘤接受了经蝶窦手术和术后放射治疗,肿瘤剂量为6650拉德。内分泌评估显示垂体功能减退。气脑造影显示气体延伸至蝶鞍腔。继发性空蝶鞍的病因尚未明确,尽管原发性空蝶鞍被认为是由于鞍膈发育不全所致。我们认为最重要的因素应该存在于鞍膈本身。可以想象,鞍膈由于以下原因而变弱:1)肿瘤压迫;2)手术中的机械损伤;3)放射效应。然后,这些先前的因素可能导致视神经和视交叉与鞍膈一起疝入蝶鞍腔。因此,我们建议垂体肿瘤的早期诊断应该很重要,并且经蝶窦手术时仔细填充鞍底对于预防继发性空蝶鞍综合征的发生至关重要。

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