Endres Dominique, Perlov Evgeniy, Stich Oliver, Tebartz van Elst Ludger
Section for Experimental Neuropsychiatry, Department of Psychiatry & Psychotherapy, Medical Center, University of Freiburg, Hauptstr. 5, 79104, Freiburg, Germany.
Department of Neurology, Medical Center, University of Freiburg, Breisacher Str. 64, 79106, Freiburg, Germany.
BMC Psychiatry. 2016 Jun 6;16:184. doi: 10.1186/s12888-016-0897-3.
Hashimoto's encephalopathy is a neuropsychiatric disease with symptoms of cognitive impairment, stroke-like episodes, seizures, and psychotic or affective symptoms associated with autoimmune thyroiditis and excellent steroid responsiveness; therefore, it is also called "steroid responsive encephalopathy associated with autoimmune thyroiditis" (SREAT).
We present the case of a 50-year-old woman who developed a first-onset depressive syndrome with predominant cognitive impairment and inability to work. Antidepressive treatment and cognitive behavioral therapy over two years were unsuccessful. Neurological examination was unremarkable. Serum analysis showed increased thyroid peroxidase and thyroglobulin antibodies. Cerebrospinal fluid protein and albumin quotient were increased. Magnetic resonance imaging depicted unspecific, supratentorial white matter lesions and frontal accentuated brain atrophy. Electroencephalography was normal. Neuropsychological testing for attentional performance was below average. High-dose intravenous treatment with methylprednisolone over 5 days and oral dose reduction over 3 weeks led to the sustained improvement of clinical symptoms. Following discharge from the hospital, the patient returned to work, and 6.5 months after the start of therapy, no neuropsychological deficit remained.
This case report illustrates that SREAT might present with purely depressive symptoms, thus mimicking classical major depression. In such cases, corticosteroid therapy may be an effective treatment option.
桥本脑病是一种神经精神疾病,具有认知障碍、类中风发作、癫痫发作以及与自身免疫性甲状腺炎相关的精神病性或情感症状,且对类固醇反应良好;因此,它也被称为“自身免疫性甲状腺炎相关性类固醇反应性脑病”(SREAT)。
我们报告一例50岁女性,首次出现以认知障碍为主且无法工作的抑郁综合征。两年的抗抑郁治疗和认知行为疗法均未成功。神经系统检查无异常。血清分析显示甲状腺过氧化物酶和甲状腺球蛋白抗体升高。脑脊液蛋白和白蛋白商数升高。磁共振成像显示非特异性幕上白质病变和额叶明显脑萎缩。脑电图正常。注意力表现的神经心理学测试低于平均水平。5天的大剂量静脉注射甲泼尼龙治疗及3周的口服剂量递减导致临床症状持续改善。出院后,患者恢复工作,治疗开始6.5个月后,神经心理学缺陷消失。
本病例报告表明,SREAT可能仅表现为抑郁症状,从而酷似典型的重度抑郁症。在这种情况下,皮质类固醇治疗可能是一种有效的治疗选择。