Bidaki Reza, Zarei Mina, Mirhosseini S M Mahdy, Moghadami Samar, Hejrati Maral, Kohnavard Marjan, Shariati Behnam
Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
Adv Biomed Res. 2012;1:61. doi: 10.4103/2277-9175.100182. Epub 2012 Aug 28.
Wilson's disease (WD) or hepatolenticular degeneration is an inherited neurodegenerative disorder of copper metabolism (autosomal recessive, chromosome13). Psychiatric disorders in WD include dementia, characterized by mental slowness, poor concentration, and memory impairment. Symptoms may progress rapidly, especially in younger patients, but are more often gradual in development with periods of remission and exacerbation. Delusional disorder and schizophrenia-like psychosis are rare forms of psychiatric presentation. In this report, the patient with WD presented by psychosis symptoms and treated mistaken as schizophrenia for almost ten years. Although he has treated with antipsychotics, he had periods of remissions and relapses and never was symptoms free. Since psychosis can be the manifestation of medical diseases such as WD, overall view of these patients is necessary and medical diseases should be considered as a differential diagnosis.
威尔逊病(WD)或肝豆状核变性是一种遗传性铜代谢神经退行性疾病(常染色体隐性遗传,位于13号染色体)。WD中的精神障碍包括痴呆,其特征为思维迟缓、注意力不集中和记忆障碍。症状可能迅速进展,尤其是在年轻患者中,但更常见的是在发展过程中逐渐出现,伴有缓解期和加重期。妄想障碍和精神分裂症样精神病是精神症状的罕见表现形式。在本报告中,该WD患者以精神病症状就诊,被误诊为精神分裂症近十年。尽管他接受了抗精神病药物治疗,但病情有缓解期和复发期,从未完全无症状。由于精神病可能是WD等医学疾病的表现,因此对这些患者进行全面评估是必要的,应将医学疾病视为鉴别诊断。