Tabarin A, Navarranne A, Guérin J, Corcuff J B, Parneix M, Roger P
Department of Endocrinology, Hôpital Haut-lévèque, Bordeaux-Pessac, France.
Clin Endocrinol (Oxf). 1991 Jan;34(1):63-9. doi: 10.1111/j.1365-2265.1991.tb01737.x.
Ketoconazole, an imidazole derivative which inhibits adrenal steroidogenesis, has been used with success for the metabolic control of Cushing's disease. Few data are available about the use of ketoconazole in the management of the ectopic ACTH syndrome. We have used ketoconazole in eight patients: four patients with Cushing's disease, two patients with overt and two with occult ectopic ACTH syndrome. Among patients with Cushing's disease, reversible hypoadrenalism occurred once. All had full clinical and biochemical regression of the disease for more than 6 months with 400-1200 mg ketoconazole per day. Patients with ectopic ACTH syndrome received 1200 mg ketoconazole per day for at least 2 months. Partial biochemical regression was observed in two and a secondary escape to adrenal blockade in two others. These findings further indicate that ketoconazole is a valuable tool for the metabolic control of Cushing's disease. On the contrary, in ectopic ACTH syndrome, this aim can be impossible to reach with ketoconazole although the reasons for its ineffectiveness remain to be determined.
酮康唑是一种抑制肾上腺类固醇生成的咪唑衍生物,已成功用于库欣病的代谢控制。关于酮康唑在异位促肾上腺皮质激素(ACTH)综合征管理中的应用,可用数据较少。我们对8例患者使用了酮康唑:4例库欣病患者,2例显性和2例隐匿性异位ACTH综合征患者。在库欣病患者中,可逆性肾上腺功能减退发生过1次。所有患者在每天使用400 - 1200毫克酮康唑的情况下,疾病均实现了完全的临床和生化缓解,持续超过6个月。异位ACTH综合征患者每天接受1200毫克酮康唑治疗至少2个月。观察到2例患者生化指标部分缓解,另外2例出现对肾上腺阻断的继发性抵抗。这些发现进一步表明,酮康唑是库欣病代谢控制的一种有价值的工具。相反,在异位ACTH综合征中,尽管酮康唑无效的原因尚待确定,但使用酮康唑可能无法实现这一目标。