首页> 美国卫生研究院文献>The Ochsner Journal >Anti–N-Methyl-D-Aspartate Receptor Encephalitis in a Patient With Antithyroid Peroxidase Antibodies and a Parotid Pleomorphic Adenoma
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Anti–N-Methyl-D-Aspartate Receptor Encephalitis in a Patient With Antithyroid Peroxidase Antibodies and a Parotid Pleomorphic Adenoma

机译:抗甲状腺过氧化物酶抗体和腮腺多形性腺瘤患者的抗N-甲基-D-天冬氨酸受体脑炎

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摘要

>Background: Anti–N-methyl-D-aspartate receptor (NMDA-R) encephalitis is an autoimmune disorder first described in 2007. It can cause severe neurologic and psychiatric symptoms, and patients often are misdiagnosed with a primary psychiatric disorder. Anti–NMDA-R encephalitis is an important differential diagnosis of psychosis, as the condition can be treated with the appropriate therapy.>Case Report: A 42-year-old female with a history of hypothyroidism presented for evaluation of agitation and weakness. Six months prior to her presentation at our hospital, she had complained of headache, and neuroimaging showed a small right frontal hyperintensity on fluid-attenuated inversion recovery imaging. Workup was largely unremarkable, and she improved briefly with steroids at the outside institution. She then developed psychiatric symptoms and had 4 admissions to separate inpatient psychiatric facilities. She was tried on various antipsychotic medications and mood stabilizers with no improvement and lost 30 pounds in 3 months. When the patient was transferred to our facility, her neuroimaging was stable, and serum and cerebrospinal fluid were positive for antithyroid peroxidase and NMDA-R antibodies. She was treated with intravenous immunoglobulin (IVIG), high-dose steroids, and rituximab. Positron emission tomography scan revealed a parotid mass that was resected and determined to be a pleomorphic adenoma. The patient improved remarkably to her baseline and was able to return to full duties at work within 6 months. In the 2 years since her initial admission, she has had minor relapses that have responded well to rituximab and IVIG.>Conclusion: This case demonstrates a typical presentation of anti–NMDA-R encephalitis, as well as the challenges that can delay diagnosis. Symptoms vary and are often psychiatric, making these patients difficult to diagnose clinically, and they therefore require thorough investigation. This case illustrates the necessity to be inquisitive and to challenge the diagnosis when a clinical picture is not congruent because an accurate diagnosis is imperative in guiding appropriate treatment.
机译:>背景:抗-N-甲基-D-天冬氨酸受体(NMDA-R)脑炎是一种自体免疫疾病,于2007年首次被描述。它可以引起严重的神经系统和精神病学症状,患者经常被误诊为原发性精神病。抗NMDA-R脑炎是一种重要的精神病鉴别诊断,因为可以通过适当的治疗方法治疗该病。>病例报告:一名具有甲状腺功能减退病史的42岁女性被提出进行评估烦躁和无力。在我们医院就诊前六个月,她主诉头痛,神经影像学表现为液体衰减型反转恢复成像显示右小额额叶高信号。体检情况基本不明显,她在外部机构使用类固醇激素后短暂改善。然后,她出现了精神病症状,并有4次入院以分别住院精神病院。她曾尝试使用各种抗精神病药物和情绪稳定剂,但均无改善,并在3个月内减掉了30磅。当患者转移到我们的设施时,她的神经影像稳定,血清和脑脊液中的抗甲状腺过氧化物酶和NMDA-R抗体呈阳性。她接受了静脉免疫球蛋白(IVIG),大剂量类固醇和利妥昔单抗的治疗。正电子发射断层扫描扫描显示腮腺肿块已切除并确定为多形性腺瘤。患者明显恢复了基线,并在6个月内恢复了工作能力。自首次入院以来的两年内,她出现了轻微复发,对利妥昔单抗和IVIG的反应良好。>结论:该病例显示了抗NMDA-R脑炎的典型表现。可能延误诊断的挑战。症状各不相同,通常是精神病,使这些患者难以临床诊断,因此需要进行彻底检查。这种情况说明,当临床情况不完全一致时,必须进行询问并质疑诊断,因为在指导适当治疗时必须进行准确的诊断。

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