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Neuropsychiatric systemic lupus erythematosus presenting as bipolar I disorder with catatonic features.

机译:神经精神系统性红斑狼疮,表现为双极性I型障碍,伴有强音特征。

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BACKGROUND: The American College of Rheumatology has defined 19 neuropsychiatric syndromes associated with systemic lupus erythematosus (SLE) involving the central, peripheral, and autonomic nervous systems. Neuropsychiatric manifestations of lupus (NPSLE) have been shown to occur in up to 95% of pediatric patients with SLE. OBJECTIVE: The authors describe a 15-year-old African American young woman with a family history positive for bipolar I disorder and schizophrenia, who presented with symptoms consistent with an affective disorder. METHOD: The patient was diagnosed with Bipolar I disorder with catatonic features and required multiple hospitalizations for mood disturbance. Two years after her initial presentation, the patient was noted to have a malar rash and subsequently underwent a full rheumatologic work-up, which revealed cerebral vasculitis. RESULTS: NPSLE was diagnosed and, after treatment with steroids, the patient improved substantially and no longer required further psychiatric medication or therapy. CONCLUSION: Given the especially high prevalence of NPSLE in pediatric patients with lupus, it is important for clinicians to recognize that neuropsychiatric symptoms in an adolescent patient may indeed be the initial manifestations of SLE, as opposed to a primary affective disorder.
机译:背景:美国风湿病学院已经定义了19种与系统性红斑狼疮(SLE)相关的神经精神综合征,涉及中枢,周围和自主神经系统。狼疮(NPSLE)的神经精神病学表现已显示在多达95%的SLE小儿患者中。目的:作者描述了一个15岁的非洲裔美国年轻妇女,她的家族史对双相性I型障碍和精神分裂症呈阳性,其症状与情感障碍一致。方法:该患者被诊断为患有双相性I障碍,具有强直性特征,需要因精神障碍多次住院。初次就诊后两年,该患者被发现患有黄斑皮疹,随后接受了全面的风湿病检查,发现了脑血管炎。结果:诊断为NPSLE,类固醇治疗后,患者明显好转,不再需要进一步的精神科药物或疗法。结论:鉴于小儿狼疮患者的NPSLE患病率特别高,因此临床医生必须认识到,与原发性情感障碍相反,青春期患者的神经精神症状确实可能是SLE的最初表现。

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