Amantadine-induced psychosis in Wilson disease.

Satish Suhas, Gaurav Kumar Singh, Vanteemar S Sreeraj, Ganesan Venkatasubramanian
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Abstract

Wilson disease is a rare genetic disorder of copper metabolism causing hepatic dysfunction and neuro-psychiatric manifestations. While psychosis in Wilson disease is uncommon, it can occur, especially with certain medications. We describe a 40-year-old woman diagnosed with Wilson disease who developed psychotic symptoms following the initiation and dose escalation of amantadine, a drug commonly used to treat parkinsonism associated with the disorder. Her symptoms included delusions of persecution, irritability and anomalous self-experiences such as 'made' phenomena, which are typically seen in schizophrenia. The psychosis resolved after discontinuing amantadine, without worsening her neurological symptoms. This underscores the importance of monitoring for psychiatric side-effects, particularly Schneiderian first-rank symptoms, in patients with Wilson disease being treated with amantadine. The findings suggest a probable adverse drug reaction, highlighting the need for careful evaluation and dose adjustments in such complex clinical cases.

金刚烷胺诱发的威尔逊氏精神病。
威尔逊病是一种罕见的铜代谢遗传性疾病,可导致肝功能障碍和神经精神表现。虽然威尔逊病的精神病并不常见,但也有可能发生,尤其是在服用某些药物时。我们描述了一名被诊断患有威尔森氏病的 40 岁女性,她在开始服用金刚烷胺并加大剂量后出现了精神病症状,金刚烷胺是一种常用于治疗与该疾病相关的帕金森氏症的药物。她的症状包括迫害妄想、易激惹和反常的自我体验,如 "制造 "现象,这是精神分裂症的典型症状。停用金刚烷胺后,她的精神病症状得到缓解,但神经系统症状并未恶化。这凸显了对接受金刚烷胺治疗的威尔逊病患者进行精神病副作用监测的重要性,尤其是施耐德一级症状。研究结果表明这可能是一种药物不良反应,强调了在这种复杂的临床病例中进行仔细评估和剂量调整的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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