Sakaguchi H, Inoue D, Kataoka K, Koshiyama H, Aoki N, Nakao K
Department of Internal Medicine, Hyogo Prefectural Amagasaki Hospital, Japan.
Endocr J. 1996 Aug;43(4):417-22. doi: 10.1507/endocrj.43.417.
We here describe two patients with empty sella syndrome who had variable and abnormal ACTH and cortisol secretory profiles. The patients are a 58-year old male and a 41-year old female, both of whom were neurotic. In both cases, low-dose dexamethasone suppression tests (1 mg, p.o., overnight) caused variable responses, such as a paradoxical increase, insufficient decrease or normal decrease in ACTH and cortisol depending on the period when they were performed. The circadian rhythm of ACTH and cortisol also showed variable patterns. Abdominal CT showed slight enlargement of both adrenal glands. Adrenal scintigraphy after dexamethasone suppression (3 mg, p.o., 7 days) revealed uptake into both adrenal glands. MRI of the brain indicated empty sella, but failed to show evidence of pituitary adenoma. It remains to be elucidated whether these secretory profiles of ACTH and cortisol in the two cases are only to be regarded as secondary changes associated with neurosis, as reported in depression or alcoholism, or the two cases share some pathogenetic mechanism with cyclic Cushing disease.
我们在此描述两名患有空蝶鞍综合征的患者,他们的促肾上腺皮质激素(ACTH)和皮质醇分泌模式各异且异常。这两名患者分别是一名58岁男性和一名41岁女性,两人均患有神经症。在这两例病例中,低剂量地塞米松抑制试验(口服1毫克,隔夜)引起了不同的反应,例如ACTH和皮质醇出现反常增加、下降不足或正常下降,这取决于进行试验的时间段。ACTH和皮质醇的昼夜节律也呈现出不同模式。腹部CT显示双侧肾上腺略有增大。地塞米松抑制(口服3毫克,7天)后的肾上腺闪烁显像显示双侧肾上腺均有摄取。脑部MRI显示为空蝶鞍,但未显示垂体腺瘤的证据。这两例病例中ACTH和皮质醇的这些分泌模式究竟仅应被视为与神经症相关的继发性变化(如在抑郁症或酒精中毒中所报道的),还是这两例病例与周期性库欣病有某些共同的发病机制,仍有待阐明。