Department of Hematology, Endocrinology and Metabolism, Faculty of Medicine, Niigata University, Niigata, Japan.
Department of Neurology, Brain Research Institute, Niigata University, Niigata, Japan.
Neuropsychiatr Dis Treat. 2014 Sep 15;10:1763-7. doi: 10.2147/NDT.S70611. eCollection 2014.
Endogenous Cushing's syndrome is an endocrine disease resulting from chronic exposure to excessive glucocorticoids produced in the adrenal cortex. Although the ultimate outcome remains uncertain, functional and morphological brain changes are not uncommon in patients with this syndrome, and generally persist even after resolution of hypercortisolemia. We present an adolescent patient with Cushing's syndrome who exhibited cognitive impairment with brain atrophy. A 19-year-old Japanese male visited a local hospital following 5 days of behavioral abnormalities, such as money wasting or nighttime wandering. He had hypertension and a 1-year history of a rounded face. Magnetic resonance imaging (MRI) revealed apparently diffuse brain atrophy. Because of high random plasma cortisol levels (28.7 μg/dL) at 10 AM, he was referred to our hospital in August 2011. Endocrinological testing showed adrenocorticotropic hormone-independent hypercortisolemia, and abdominal computed tomography demonstrated a 2.7 cm tumor in the left adrenal gland. The patient underwent left adrenalectomy in September 2011, and the diagnosis of cortisol-secreting adenoma was confirmed histologically. His hypertension and Cushingoid features regressed. Behavioral abnormalities were no longer observed, and he was classified as cured of his cognitive disturbance caused by Cushing's syndrome in February 2012. MRI performed 8 months after surgery revealed reversal of brain atrophy, and his subsequent course has been uneventful. In summary, the young age at onset and the short duration of Cushing's syndrome probably contributed to the rapid recovery of both cognitive dysfunction and brain atrophy in our patient. Cushing's syndrome should be considered as a possible etiological factor in patients with cognitive impairment and brain atrophy that is atypical for their age.
内源性库欣综合征是一种由肾上腺皮质产生的慢性暴露于过多糖皮质激素引起的内分泌疾病。尽管最终结果仍不确定,但患有这种综合征的患者通常会出现功能性和形态学脑改变,并且这些改变通常在高皮质醇血症缓解后仍持续存在。我们报告了一例伴有脑萎缩的库欣综合征青少年患者,该患者表现出认知障碍。一名 19 岁的日本男性因行为异常(如乱花钱或夜间游荡)就诊于当地医院,持续了 5 天。他患有高血压和 1 年的圆脸病史。磁共振成像(MRI)显示明显弥漫性脑萎缩。由于上午 10 点时随机血浆皮质醇水平较高(28.7μg/dL),他于 2011 年 8 月被转至我院。内分泌检查显示促肾上腺皮质激素非依赖性皮质醇增多症,腹部计算机断层扫描显示左侧肾上腺有 2.7cm 肿瘤。患者于 2011 年 9 月接受了左肾上腺切除术,组织学证实为皮质醇分泌腺瘤。他的高血压和库欣样特征消退。行为异常不再观察到,他被归类为 2012 年 2 月因库欣综合征引起的认知障碍治愈。术后 8 个月进行的 MRI 显示脑萎缩逆转,随后的病程平稳。总之,发病年龄较轻和库欣综合征持续时间较短可能导致我们患者的认知功能障碍和脑萎缩迅速恢复。在认知障碍和脑萎缩不典型的患者中,应考虑库欣综合征为可能的病因。