Lindholm J
Department of Neurosurgery NK 2091, Rigshospitalet-University Hospital, Copenhagen, Denmark.
Clin Endocrinol (Oxf). 1992 Feb;36(2):151-9. doi: 10.1111/j.1365-2265.1992.tb00950.x.
To estimate the value of some commonly used tests in diagnosing Cushing's disease and to assess the outcome after treatment.
Follow-up of a consecutive group of patients for 4.1 to 109.6 months, median 34.4.
Forty-six patients assumed to have ACTH dependent hypercorticism (of 50 patients with Cushing's syndrome) were included. Forty-five underwent transsphenoidal neurosurgery. Ten were treated preoperatively with radiotherapy.
Pituitary, adrenal, thyroid and gonadal function, radiology and pituitary histology were evaluated.
One main finding was a significant correlation between the urinary excretion of cortisol before and during administration of dexamethasone. Thus patients with modestly elevated urinary cortisol excretion had an apparently normal suppression. The urinary cortisol values during the dexamethasone test were significantly related to the peak plasma cortisol concentrations at the 30-minute ACTH tests. Computed tomography failed to identify an adenoma in 10 of the 19 patients who were histologically proved to harbour a corticotroph adenoma. At 6 months after radiotherapy, clinical and biochemical improvement was noted in none. Cure was achieved in 36 after neurosurgery. Eventually, adrenalectomy was needed in eight patients. Sixteen patients developed persisting adrenal insufficiency after neurosurgery so that the total number of patients on permanent steroid substitution was 24. Post-operative thyroid and gonadal insufficiency (in men and women of fertile age) was found in 36 and 49%, respectively.
The diagnostic value of measuring the cortisol excretion during dexamethasone administration appears doubtful. The outcome after neurosurgical treatment for Cushing's disease is not entirely satisfactory. Further studies are needed to decide whether adrenalectomy as the first line of therapy should be considered relevant in some patients with Cushing's disease.
评估一些常用检查在库欣病诊断中的价值,并评估治疗后的结果。
对一组连续患者进行4.1至109.6个月的随访,中位数为34.4个月。
纳入了50例库欣综合征患者中46例假定为促肾上腺皮质激素(ACTH)依赖性皮质醇增多症的患者。45例接受了经蝶窦神经外科手术。10例术前接受了放射治疗。
评估垂体、肾上腺、甲状腺和性腺功能、放射学及垂体组织学。
一个主要发现是地塞米松给药前和给药期间尿皮质醇排泄之间存在显著相关性。因此,尿皮质醇排泄轻度升高的患者有明显正常的抑制作用。地塞米松试验期间的尿皮质醇值与30分钟促肾上腺皮质激素试验时的血浆皮质醇峰值浓度显著相关。计算机断层扫描未能在19例经组织学证实患有促肾上腺皮质激素腺瘤的患者中的10例中识别出腺瘤。放疗后6个月,未观察到临床和生化改善。神经外科手术后36例治愈。最终,8例患者需要进行肾上腺切除术。16例患者神经外科手术后出现持续性肾上腺功能不全,因此接受永久性类固醇替代治疗的患者总数为24例。术后甲状腺和性腺功能不全(在育龄男性和女性中)分别在36%和49%的患者中发现。
测量地塞米松给药期间皮质醇排泄的诊断价值似乎存疑。库欣病神经外科治疗后的结果并不完全令人满意。需要进一步研究以确定肾上腺切除术作为一线治疗方法是否应在某些库欣病患者中被视为合理。