以强直为表现的与自身免疫性甲状腺炎相关的脑病:一例报告和文献复习。

IF 1.3 4区 医学 Q3 PSYCHIATRY
Hossam Tharwat Ali, Farah Riyad Mohamed, Ahmed Khaled Al-Ghannami, Ana Leticia Fornari Caprara, Jamir Pitton Rissardo
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引用次数: 0

摘要

脑病可与自身免疫性疾病相关,如自身免疫性甲状腺炎,并可表现为广泛的神经精神表现。然而,它很少表现为紧张症。我们报告一例中年女性桥本甲状腺炎伴紧张症。还包括对以前类似案例的文献综述,突出了重要的观点。一名48岁的女性因紧张症状在前5天恶化而被送往急诊科。据报道,类似的情况在3个月前发生并自行缓解。检查时,患者表现出不配合和无反应。她表现出典型的紧张症症状,在布什-弗朗西斯紧张症评定量表上得了21分。常规检查在正常范围内,除了C反应蛋白水平升高和红细胞沉降率升高。计算机断层扫描、磁共振成像和脑脊液分析均正常。脑电图显示弥漫性Δθ范围减慢,无癫痫样放电。服用洛拉西泮,但并未控制紧张症状。重新评估显示甲状腺肿胀,甲状腺过氧化物酶抗体水平升高。因此,开始静脉注射甲基强的松龙,并在4小时内完全缓解紧张症状。患者出院后,每天服用1 mg/kg的泼尼松。在随访中,患者继续表现出紧张症状的完全缓解。值得注意的是,该患者在该紧张性发作6个月后出现甲状腺功能减退,为此开具了50mcg/d的左旋甲状腺素处方。与自身免疫性甲状腺炎相关的脑病在甲状腺功能正常的病例中最初可表现为紧张性症状。主要的治疗方法是类固醇,它可以完全缓解紧张症状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Catatonia as the Presentation of Encephalopathy Associated With Autoimmune Thyroiditis: A Case Report and Literature Review.

Encephalopathy can be associated with autoimmune disorders such as autoimmune thyroiditis, and it can present with a wide range of neuropsychiatric manifestations. However, it rarely presents with catatonia. We present the case of a middle-aged female with Hashimoto's thyroiditis presenting with catatonia. A literature review of previous similar cases highlighting significant points is also included. A 48-year-old female presented to the emergency department with catatonic symptoms that had worsened over the previous 5 days. A similar condition was reported to have occurred and resolved spontaneously 3 months earlier. On examination, the patient appeared uncooperative and unresponsive. She showed typical symptoms of catatonia, with a score of 21 points on the Bush-Francis Catatonia Rating Scale. Routine tests were within normal ranges except for an elevated level of C-reactive protein and an elevated erythrocyte sedimentation rate. Computed tomography, magnetic resonance imaging, and cerebrospinal fluid analysis were all normal. An electroencephalogram showed diffuse delta-theta range slowing with no epileptiform discharges. Lorazepam was initiated but did not control the catatonic symptoms. Re-evaluation revealed thyroid swelling and elevated levels of thyroperoxidase antibodies. IV methylprednisolone was therefore initiated and produced complete resolution of the catatonic symptoms in 4 hours. The patient was discharged and prescribed prednisone 1 mg/kg daily. At follow-up, the patient continued to show complete resolution of the catatonic symptoms. It is noteworthy that the patient developed hypothyroidism 6 months after this catatonic episode for which levothyroxine 50 mcg/d was prescribed. Encephalopathy associated with autoimmune thyroiditis can initially present with catatonic symptoms in euthyroid cases. The mainstay of treatment is steroids which result in complete resolution of the catatonic symptoms.

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来源期刊
CiteScore
2.30
自引率
10.50%
发文量
159
审稿时长
>12 weeks
期刊介绍: Journal of Psychiatric Practice® seizes the day with its emphasis on the three Rs — readability, reliability, and relevance. Featuring an eye-catching style, the journal combines clinically applicable reviews, case studies, and articles on treatment advances with practical and informative tips for treating patients. Mental health professionals will want access to this review journal — for sharpening their clinical skills, discovering the best in treatment, and navigating this rapidly changing field. Journal of Psychiatric Practice combines clinically applicable reviews, case studies, and articles on treatment advances with informative "how to" tips for surviving in a managed care environment.
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