Suppr超能文献

库欣病的经蝶窦手术:切除的组织决定内分泌结果吗?

Transsphenoidal surgery for Cushing's disease: does what is removed determine the endocrine outcome?

作者信息

Burke C W, Adams C B, Esiri M M, Morris C, Bevan J S

机构信息

Department of Endocrinology, Radcliffe Infirmary, Oxford, UK.

出版信息

Clin Endocrinol (Oxf). 1990 Oct;33(4):525-37. doi: 10.1111/j.1365-2265.1990.tb03890.x.

Abstract

Fifty-seven patients with pituitary-dependent Cushing's syndrome and eight with Nelson's syndrome underwent transsphenoidal pituitary exploration, with removal of macroscopically abnormal tissue in 64 patients and detailed histology of this in 63. The cure rate by stringent criteria 1 month later was 48 (83%) of the 58 with assessable data, who were followed for 225 patient-years. Two patients relapsed later, a rate of one per 112 patient-years of follow-up. In 27% of patients, the macroscopically abnormal tissue removed was histologically indistinguishable from normal pituitary gland but the cure rate was 82%, and a quarter of the patients in this group assessable for recovery of normal ACTH function gained it. Another 53% of biopsies showed corticotroph adenomas, and the cure rate in these was 89% though rather more (69%) recovered normal ACTH function. The remaining 20% of biopsies were consistent with corticotroph hyperplasia. The cure rate varied little whether the lesion was diffuse or localized, whether or not it was in the invasion zone/interlobar cleft, whether or not there was pituitary enlargement, or whether the surgery was radical or selective. Six patients, of whom three are cured, showed surgical or radiological evidence of invasion outside the pituitary fossa. The data are consistent with the idea that pituitary adenoma is merely the end stage of some other process in the corticotrophs, and cure often follows removal of a lesion other than adenoma. Of patients who were permanently cured, 47% regained normal ACTH function within 3 years of operation (none later), 53% remaining ACTH-deficient at 3 years or more. Of all patients 48% acquired gonadotrophin deficiency, 28% have TSH deficiency and 25% permanent diabetes insipidus. All these pituitary function deficits were more common after radical surgery and in patients with normal histology, The literature contains so little objective data on these functions that we cannot say whether the endocrine damage in our patients is exceptional or not.

摘要

57例垂体依赖性库欣综合征患者和8例纳尔逊综合征患者接受了经蝶窦垂体探查术,64例患者切除了肉眼可见的异常组织,其中63例进行了详细的组织学检查。1个月后,按照严格标准,58例有可评估数据的患者中,48例(83%)治愈,这些患者的随访时间为225患者年。2例患者后来复发,随访期间每112患者年复发率为1例。在27%的患者中,切除的肉眼可见异常组织在组织学上与正常垂体腺无法区分,但治愈率为82%,该组中可评估促肾上腺皮质激素(ACTH)功能恢复情况的患者中有四分之一恢复了正常功能。另外53%的活检显示为促肾上腺皮质激素腺瘤,这些患者的治愈率为89%,不过恢复正常ACTH功能的比例更高(69%)。其余20%的活检结果符合促肾上腺皮质激素细胞增生。无论病变是弥漫性还是局限性,是否位于侵袭区/叶间裂,是否存在垂体增大,或者手术是根治性还是选择性的,治愈率变化不大。6例患者有垂体窝外侵袭的手术或影像学证据,其中3例治愈。这些数据与垂体腺瘤仅仅是促肾上腺皮质激素细胞中其他一些过程的终末期这一观点一致,而且治愈通常是在切除腺瘤以外的病变之后。在永久治愈的患者中,47%在术后3年内恢复了正常ACTH功能(之后无复发),53%在3年或更长时间仍存在ACTH缺乏。所有患者中,48%出现促性腺激素缺乏,28%有促甲状腺激素缺乏,25%有永久性尿崩症。所有这些垂体功能缺陷在根治性手术后以及组织学正常的患者中更为常见。文献中关于这些功能的客观数据非常少,以至于我们无法确定我们患者中的内分泌损伤是否异常。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验