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库欣病与原发性空蝶鞍的关联。

The association of Cushing's disease and primary empty sella turcica.

作者信息

Manavela M P, Goodall C M, Katz S B, Moncet D, Bruno O D

机构信息

División Endocrinología, Hospital de Clínicas, Buenos Aires University, Ciudad de Buenos Aires, Argentina.

出版信息

Pituitary. 2001 Aug;4(3):145-51. doi: 10.1023/a:1015310806063.

Abstract

The empty sella turcica is defined as the extension of the subarachnoid space toward the intrasellar region with displacement of the pituitary towards the posteroinferior wall. By autopsy studies, the incidence in the general population is around 20%. The association of Cushing's disease (CD) and empty sella has been infrequently reported. In our group, from a total of 68 patients with CD studied by magnetic resonance imaging (MRI), we found the presence of a primary empty sella syndrome (ESS) in 11 (16%). Of these, 9 had partial and 2 total ESS, and in four of them a microadenoma could be identified. Remission, ascertained by subnormal postoperative cortisol levels in blood and/or urine was obtained in 5 of 6 patients operated on by the transphenoidal route. Following surgery, 2 patients presented cerebrospinal fluid (CSF) leakage, 2 diabetes insipidus, and 2 some form of hypopituitarism, figures apparently higher than in non-ESS patients with CD. Ketoconazole was indicated as second line treatment in 2 patients and as primary therapy in 4, resulting in normal urinary free cortisol (UFC) values, with no complications. The relationship of ESS and CD is probably fortuitous given that the frequency of ESS in the general population is similar. Although in empty sella both surgery and radiotherapy seem to have greater risk of complications, surgery remains the first line treatment. Nevertheless, chronic treatment with ketoconazole could be a useful first choice, particularly when no adenoma is seen, or in those who have contraindications for surgery.

摘要

空蝶鞍被定义为蛛网膜下腔向鞍内区域延伸,同时垂体向鞍后下壁移位。通过尸检研究,普通人群中的发病率约为20%。库欣病(CD)与空蝶鞍的关联鲜有报道。在我们的研究组中,对68例经磁共振成像(MRI)检查的CD患者进行研究,发现11例(16%)存在原发性空蝶鞍综合征(ESS)。其中,9例为部分性ESS,2例为完全性ESS,且在其中4例中可识别出微腺瘤。6例经蝶窦手术的患者中有5例术后血和/或尿皮质醇水平低于正常,从而确定达到缓解。术后,2例患者出现脑脊液(CSF)漏,2例出现尿崩症,2例出现某种形式的垂体功能减退,这些数字明显高于非ESS的CD患者。2例患者将酮康唑作为二线治疗,4例作为一线治疗,结果尿游离皮质醇(UFC)值正常,且无并发症。ESS与CD的关系可能是偶然的,因为普通人群中ESS的发生率相似。尽管在空蝶鞍中,手术和放疗似乎都有更高的并发症风险,但手术仍然是一线治疗方法。然而,酮康唑长期治疗可能是一种有用的首选方法,特别是在未发现腺瘤或有手术禁忌证的患者中。

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