Alicia R. Khan , Jacob Carolan , Mario J. Rullo , Kelly L. Hamilton , Tamara Movsesova , Barsegh A. Barseghian , Pauline Tsai , Jennifer F. Schreiber
{"title":"与自身免疫性甲状腺炎相关的类固醇反应性脑病(SREAT)表现为恶性兴奋性紧张症:一种新的临床表现","authors":"Alicia R. Khan , Jacob Carolan , Mario J. Rullo , Kelly L. Hamilton , Tamara Movsesova , Barsegh A. Barseghian , Pauline Tsai , Jennifer F. Schreiber","doi":"10.1016/j.psycr.2023.100198","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Hashimoto Encephalopathy, more accurately known as Steroid Responsive Encephalopathy associated with Autoimmune Thyroiditis (SREAT), is an exceedingly rare and often controversial diagnosis that, when present, manifests as encephalopathy with a variety of other potential symptoms in the setting of elevated antithyroid peroxidase antibody and/or antithyroglobulin antibody. Its manifestations can include encephalopathy, seizures, myoclonus, hallucinations, stroke-like findings, and more.</p></div><div><h3>Patient case</h3><p>We present the case of a 39-year-old transgender man with autistic spectrum disorder and depression, initially presumed to be in acute psychiatric decompensation, later found to have elevated levels of anti-thyroid peroxidase antibodies, who responded well to plasma exchange (PLEX) and rituximab. On initial psychiatric admission, the patient had symptoms of suicidal ideation, confusion, and agitation. He showed little improvement on medications such as quetiapine, olanzapine, valproate, and bupropion. Due to worsening agitation and cognitive impairment, he required further medical and neurological evaluation. He later had an episode deemed to be a likely seizure. This workup included electroencephalogram (EEG), MRI Brain, and lumbar puncture, yet all were unremarkable. Laboratory values were notable for elevated serum anti-thyroid peroxidase (TPO) antibodies of 661 U/mL. The patient received intravenous high-dose steroids with transient improvement. He eventually responded dramatically to plasmapheresis and rituximab. At his post-discharge follow up, he had returned to his cognitive baseline. He successfully resumed his job and has since remained at his functional baseline.</p></div><div><h3>Conclusion</h3><p>This case is the first to our knowledge to characterize a novel presentation of SREAT mimicking malignant excited catatonia. In such cases, if initial response to glucocorticoid treatment is equivocal, plasma exchange may be an effective treatment option.</p></div>","PeriodicalId":74594,"journal":{"name":"Psychiatry research case reports","volume":"3 1","pages":"Article 100198"},"PeriodicalIF":0.0000,"publicationDate":"2023-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2773021223000962/pdfft?md5=cdc8a3c10578a58e5aaea2427b16d459&pid=1-s2.0-S2773021223000962-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Steroid-Responsive Encephalopathy associated with Autoimmune Thyroiditis (SREAT) presenting as malignant excited catatonia: A novel clinical presentation\",\"authors\":\"Alicia R. Khan , Jacob Carolan , Mario J. Rullo , Kelly L. Hamilton , Tamara Movsesova , Barsegh A. Barseghian , Pauline Tsai , Jennifer F. Schreiber\",\"doi\":\"10.1016/j.psycr.2023.100198\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Hashimoto Encephalopathy, more accurately known as Steroid Responsive Encephalopathy associated with Autoimmune Thyroiditis (SREAT), is an exceedingly rare and often controversial diagnosis that, when present, manifests as encephalopathy with a variety of other potential symptoms in the setting of elevated antithyroid peroxidase antibody and/or antithyroglobulin antibody. Its manifestations can include encephalopathy, seizures, myoclonus, hallucinations, stroke-like findings, and more.</p></div><div><h3>Patient case</h3><p>We present the case of a 39-year-old transgender man with autistic spectrum disorder and depression, initially presumed to be in acute psychiatric decompensation, later found to have elevated levels of anti-thyroid peroxidase antibodies, who responded well to plasma exchange (PLEX) and rituximab. On initial psychiatric admission, the patient had symptoms of suicidal ideation, confusion, and agitation. He showed little improvement on medications such as quetiapine, olanzapine, valproate, and bupropion. Due to worsening agitation and cognitive impairment, he required further medical and neurological evaluation. He later had an episode deemed to be a likely seizure. This workup included electroencephalogram (EEG), MRI Brain, and lumbar puncture, yet all were unremarkable. Laboratory values were notable for elevated serum anti-thyroid peroxidase (TPO) antibodies of 661 U/mL. The patient received intravenous high-dose steroids with transient improvement. He eventually responded dramatically to plasmapheresis and rituximab. At his post-discharge follow up, he had returned to his cognitive baseline. He successfully resumed his job and has since remained at his functional baseline.</p></div><div><h3>Conclusion</h3><p>This case is the first to our knowledge to characterize a novel presentation of SREAT mimicking malignant excited catatonia. In such cases, if initial response to glucocorticoid treatment is equivocal, plasma exchange may be an effective treatment option.</p></div>\",\"PeriodicalId\":74594,\"journal\":{\"name\":\"Psychiatry research case reports\",\"volume\":\"3 1\",\"pages\":\"Article 100198\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-11-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2773021223000962/pdfft?md5=cdc8a3c10578a58e5aaea2427b16d459&pid=1-s2.0-S2773021223000962-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Psychiatry research case reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2773021223000962\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Psychiatry research case reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2773021223000962","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Steroid-Responsive Encephalopathy associated with Autoimmune Thyroiditis (SREAT) presenting as malignant excited catatonia: A novel clinical presentation
Background
Hashimoto Encephalopathy, more accurately known as Steroid Responsive Encephalopathy associated with Autoimmune Thyroiditis (SREAT), is an exceedingly rare and often controversial diagnosis that, when present, manifests as encephalopathy with a variety of other potential symptoms in the setting of elevated antithyroid peroxidase antibody and/or antithyroglobulin antibody. Its manifestations can include encephalopathy, seizures, myoclonus, hallucinations, stroke-like findings, and more.
Patient case
We present the case of a 39-year-old transgender man with autistic spectrum disorder and depression, initially presumed to be in acute psychiatric decompensation, later found to have elevated levels of anti-thyroid peroxidase antibodies, who responded well to plasma exchange (PLEX) and rituximab. On initial psychiatric admission, the patient had symptoms of suicidal ideation, confusion, and agitation. He showed little improvement on medications such as quetiapine, olanzapine, valproate, and bupropion. Due to worsening agitation and cognitive impairment, he required further medical and neurological evaluation. He later had an episode deemed to be a likely seizure. This workup included electroencephalogram (EEG), MRI Brain, and lumbar puncture, yet all were unremarkable. Laboratory values were notable for elevated serum anti-thyroid peroxidase (TPO) antibodies of 661 U/mL. The patient received intravenous high-dose steroids with transient improvement. He eventually responded dramatically to plasmapheresis and rituximab. At his post-discharge follow up, he had returned to his cognitive baseline. He successfully resumed his job and has since remained at his functional baseline.
Conclusion
This case is the first to our knowledge to characterize a novel presentation of SREAT mimicking malignant excited catatonia. In such cases, if initial response to glucocorticoid treatment is equivocal, plasma exchange may be an effective treatment option.