Endres Dominique, Perlov Evgeniy, Riering Anne Nicole, Maier Viktoria, Stich Oliver, Dersch Rick, Venhoff Nils, Erny Daniel, Mader Irina, Tebartz van Elst Ludger
Faculty of Medicine, Department of Psychiatry, Section for Experimental Neuropsychiatry, University of Freiburg, Freiburg, Germany.
Clinic for Psychiatry Luzern, Luzern, Switzerland.
Front Psychiatry. 2017 Apr 21;8:64. doi: 10.3389/fpsyt.2017.00064. eCollection 2017.
Schizophreniform syndromes can be divided into primary forms from polygenic causes or secondary forms due to immunological, epileptiform, monogenic, or degenerative causes. Steroid-responsive encephalopathy associated with autoimmune thyroiditis (SREAT) is a secondary immunological form associated with increased thyroid antibodies, such as antithyroid peroxidase antibodies and shows a good response to corticosteroids.
We present the case of a 41-year-old woman suffering from a schizophreniform syndrome. Starting at the age of 35, she developed psychotic exacerbations with formal thought disorder, acoustic hallucinations, cenesthopathic experiences, and loss of ego boundaries. At the same time, she began to suffer from chronic sexual delusions and olfactory hallucinations, which did not respond to neuroleptic medication. Her levels of antithyroid peroxidase antibodies were slightly increased, and the blood-brain barrier was disturbed. An electroencephalogram (EEG) showed intermittent generalized slowing, and cerebral magnetic resonance imaging (cMRI) depicted mild temporolateral atrophy. High-dose corticosteroid treatment led to convincing improvement of attentional performance and the disappearance of delusions and olfactory hallucinations.
SREAT can mimic typical symptoms of schizophreniform syndromes. The increased titer of antithyroid peroxidase antibodies in combination with the EEG slowing, blood-brain barrier dysfunction, and the cMRI alterations were the basis for suspecting an immunological cause in our patient. Chronic delusions, olfactory hallucinations, and cognitive deficits were successfully treated with corticosteroids. The occurrence of secondary immunological forms of schizophreniform syndromes demonstrates the need for innovative immunosuppressive treatment options.
精神分裂症样综合征可分为由多基因原因引起的原发性形式或由免疫、癫痫样、单基因或退行性原因引起的继发性形式。自身免疫性甲状腺炎相关性类固醇反应性脑病(SREAT)是一种继发性免疫形式,与甲状腺抗体如抗甲状腺过氧化物酶抗体升高有关,对皮质类固醇治疗反应良好。
我们报告一例患有精神分裂症样综合征的41岁女性病例。35岁起,她出现伴有形式思维障碍、幻听、内感性不适及自我界限丧失的精神病性发作。同时,她开始出现慢性性妄想和幻嗅,抗精神病药物治疗无效。她的抗甲状腺过氧化物酶抗体水平略有升高,血脑屏障受到干扰。脑电图(EEG)显示间歇性广泛性减慢,脑磁共振成像(cMRI)显示轻度颞外侧萎缩。高剂量皮质类固醇治疗使注意力明显改善,妄想和幻嗅消失。
SREAT可模仿精神分裂症样综合征的典型症状。抗甲状腺过氧化物酶抗体滴度升高,结合EEG减慢、血脑屏障功能障碍及cMRI改变,是怀疑我们患者存在免疫原因的依据。慢性妄想、幻嗅和认知缺陷通过皮质类固醇治疗成功得到改善。精神分裂症样综合征继发性免疫形式的出现表明需要创新的免疫抑制治疗方案。