Obsessive‐compulsive disorder as an initial manifestation of anti‐glutamic acid decarboxylase antibody‐associated encephalitis

IF 0.4 Q4 CLINICAL NEUROLOGY Neurology and Clinical Neuroscience Pub Date : 2024-05-17 DOI:10.1111/ncn3.12830
Naoki Yamahara, N. Yoshikura, Akio Kimura, Mayu Sakai, Daisuke Yabe, T. Shimohata
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Abstract

We present the case of a 44‐year‐old woman with type 1 diabetes and anti‐glutamic acid decarboxylase antibody (GAD‐Ab) (6100 U/mL in serum), manifesting as a one‐month history of compulsive writing in her self‐monitoring blood glucose (SMBG) diary and a one‐week history of seizures before admission. On admission, she was diagnosed with GAD‐Ab‐associated encephalitis (GAD‐AE), and compulsive writing consistent with obsessive‐compulsive disorder (OCD) caused by a repetitive and persistent urge to neutralize anxiety manifesting as clearly excessive writing. Immunotherapy, including corticosteroids, azathioprine, and intravenous immunoglobulin, improved her compulsive writing, and seizures disappeared following lacosamide treatment. Two months after discharge, compulsive writing reappeared and the patient was successfully treated with temporary immunotherapy intensification. After a stable period of 2 years, the patient died due to hypoglycemic encephalopathy. Overall, we showed that GAD‐AE may cause OCD.
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作为抗谷氨酸脱羧酶抗体相关脑炎初期表现的强迫症
本病例是一名 44 岁女性患者,患有 1 型糖尿病和抗谷氨酸脱羧酶抗体 (GAD-Ab)(血清中含量为 6100 U/mL),表现为在自我监测血糖 (SMBG) 日记中强迫性书写一个月,入院前有一周的癫痫发作史。入院时,她被诊断为 GAD-Ab相关脑炎(GAD-AE),强迫性书写与强迫症(OCD)一致,是由于反复、持续的中和焦虑的冲动引起的,表现为明显的过度书写。包括皮质类固醇、硫唑嘌呤和静脉注射免疫球蛋白在内的免疫疗法改善了她的强迫性书写,拉科酰胺治疗后癫痫发作也消失了。出院两个月后,强迫性书写再次出现,患者接受了临时加强免疫治疗,并取得了成功。病情稳定两年后,患者因低血糖脑病死亡。总之,我们的研究表明,GAD-AE 可能会导致强迫症。
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76
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