Bochicchio D, Losa M, Buchfelder M
Institute of Endocrine Sciences, Ospedale Maggiore IRCCS, Milan, Italy.
J Clin Endocrinol Metab. 1995 Nov;80(11):3114-20. doi: 10.1210/jcem.80.11.7593411.
Hypercortisolism attributable to hypersecretion of ACTH by a pituitary adenoma is an uncommon and progressively lethal disease. Because of its rarity, it has been difficult to collect a large series of patients in order to identify the prognostic factors influencing the outcome after transsphenoidal surgery. We conducted a multicenter, retrospective analysis of the early and late results of surgical treatment of Cushing's disease. Files of patients with Cushing's disease who underwent transsphenoidal surgery between 1975 and 1990 were collected from 25 institutions throughout Europe. Data from 668 of 716 patients were suitable for statistical analyses. Surgical mortality was 1.9%, and major morbidity occurred in 97 patients (14.5%). Clinical and biochemical remission of Cushing's disease after surgery occurred in 510 cases (76.3%). Identification of the tumor by neuroradiological imaging or at operation with histopathological corroboration was associated with remission of hypercortisolism. Recurrence of the disease occurred in 65 (12.7%) of 510 patients in remission after surgery at a mean time of 39.3 months (range 6-104 months). The distribution of the recurrences did not show any apparent plateau or cluster throughout the follow-up period. Low postoperative steroid levels, absence of cortisol response to CRH, and the need for long-term glucocorticoid substitution therapy were all associated with a high probability of long-term remission. Our study demonstrates that transsphenoidal surgery is a safe and effective treatment for patients with Cushing's disease. However, after successful surgery there is a steady increase in the percentage of recurrences, which continues with time. Patients who after operation had hypoadrenocorticism and needed long-term glucocorticoid substitution therapy had the lowest risk of relapse.
由垂体腺瘤分泌促肾上腺皮质激素过多引起的皮质醇增多症是一种罕见且逐渐致命的疾病。由于其罕见性,很难收集到大量患者以确定影响经蝶窦手术后预后的因素。我们对库欣病手术治疗的早期和晚期结果进行了多中心回顾性分析。从欧洲各地的25家机构收集了1975年至1990年间接受经蝶窦手术的库欣病患者的病历。716例患者中的668例数据适合进行统计分析。手术死亡率为1.9%,97例患者(14.5%)发生了严重并发症。手术后库欣病的临床和生化缓解发生在510例(76.3%)。通过神经放射学成像或手术时经组织病理学证实识别肿瘤与皮质醇增多症的缓解相关。510例手术后缓解的患者中有65例(12.7%)疾病复发,平均复发时间为39.3个月(范围6 - 104个月)。在整个随访期间,复发的分布没有显示出任何明显的平台期或聚集现象。术后类固醇水平低、对促肾上腺皮质激素释放激素无皮质醇反应以及需要长期糖皮质激素替代治疗均与长期缓解的高概率相关。我们的研究表明,经蝶窦手术是治疗库欣病患者的一种安全有效的方法。然而,成功手术后复发率稳步上升,且随时间持续。术后患有肾上腺皮质功能减退症且需要长期糖皮质激素替代治疗的患者复发风险最低。