Berwaerts J J, Verhelst J A, Verhaert G C, Verhaegen A A, Abs R E
Department of Endocrinology, Middelheim Hospital, Antwerp, Belgium.
J Am Geriatr Soc. 1998 Jul;46(7):880-4. doi: 10.1111/j.1532-5415.1998.tb02723.x.
Cushing's syndrome is a rare disorder. The corticotropin (ACTH)-dependent form of this syndrome generally results either from excessive ACTH secretion by a pituitary adenoma or ectopic secretion by a malignant tumor. Theoretically, the latter type can be assumed to occur more frequently in old age as the incidence of malignancy increases.
Diagnostic procedures for these five cases of Cushing's syndrome consisted of 24-hour urinary cortisol excretion, plasma ACTH and serum cortisol levels, oCRH stimulatory test, low-dose and high-dose dexamethasone suppression tests, CT scan or MR imaging of the pituitary region, and bilateral inferior petrosal sinus sampling. Patients were treated with ketoconazole, if possible, and evaluated according to clinical response and 24-hour urinary cortisol excretion.
The five cases presented were selected on the basis of age--75 years or older--from a total of about 100 patients presenting with Cushing's syndrome. In only three cases were signs of hypercorticism found on clinical examination. The other two patients were evaluated for adrenocortical excess because of severe hypokalemia and the fortuitous finding of enlarged adrenal glands on CT scan, respectively.
As a result of endocrine testing, pituitary-dependent Cushing's disease was suspected in three patients and ectopic Cushing's syndrome in two patients. Imaging techniques demonstrated only one pituitary adenoma in the first three patients and a lung tumor in one of the latter two patients. Inferior petrosal sinus sampling confirmed the suspected origin of the Cushing's syndrome in the three patients in which this procedure was performed. All three patients with pituitary-dependent Cushing's disease underwent successful clinical and biochemical treatment with ketoconazole.
Pituitary-dependent Cushing's disease may occur more frequently in patients older than 75 years of age than has previously been assumed. Because surgical treatment is not always easily tolerated by older patients, the steroidogenesis inhibitor, ketoconazole, can be a valuable alternative for the control of hypercorticism.
库欣综合征是一种罕见疾病。该综合征的促肾上腺皮质激素(ACTH)依赖型通常源于垂体腺瘤过度分泌ACTH或恶性肿瘤异位分泌。从理论上讲,随着恶性肿瘤发病率上升,后一种类型在老年人群中可能更常见。
这5例库欣综合征患者的诊断程序包括24小时尿皮质醇排泄量、血浆ACTH和血清皮质醇水平、促肾上腺皮质激素释放激素(oCRH)刺激试验、小剂量和大剂量地塞米松抑制试验、垂体区域的CT扫描或磁共振成像(MR成像)以及双侧岩下窦采血。如有可能,患者接受酮康唑治疗,并根据临床反应和24小时尿皮质醇排泄量进行评估。
这5例患者是从总共约100例库欣综合征患者中,按照年龄在75岁及以上挑选出来的。临床检查仅在3例中发现皮质醇增多症迹象。另外2例患者分别因严重低钾血症和CT扫描偶然发现肾上腺增大而接受肾上腺皮质功能亢进评估。
内分泌检测结果显示,3例患者疑似垂体依赖性库欣病,2例患者疑似异位库欣综合征。成像技术在前3例患者中仅发现1例垂体腺瘤,后2例患者中的1例发现肺部肿瘤。岩下窦采血证实了3例接受该检查的患者库欣综合征的疑似病因。所有3例垂体依赖性库欣病患者均通过酮康唑成功进行了临床和生化治疗。
垂体依赖性库欣病在75岁以上患者中的发生率可能比之前认为的更高。由于老年患者不一定总能耐受手术治疗,类固醇生成抑制剂酮康唑可作为控制皮质醇增多症的一种有价值的替代方法。