[冰冻素相关周期性发热综合征(CAPS)表现为早发性痴呆,缺乏典型的复发性发热或皮疹:病例报告]。

Q4 Medicine Clinical Neurology Pub Date : 2024-06-27 Epub Date: 2024-05-25 DOI:10.5692/clinicalneurol.cn-001956
Tomone Taneda, Mizuki Takahashi, Maiko Umeda, Yoshitaka Umeda, Mutsuo Oyake, Ryuta Nishikomori, Nobuya Fujita
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引用次数: 0

摘要

本院收治了一名 54 岁的男性患者,他拥有大学学位,因渐进性痴呆症已有两年病史。他患有家族性感音神经性听力损失,从 30 多岁起就开始接受癫痫治疗。入院时,他出现了严重的痴呆和帕金森症,但没有发烧或皮疹。全身炎症明显,CSF细胞计数和IL-6水平分别升高至53/μl和307 ‍pg/ml。脑部磁共振成像显示弥漫性脑萎缩。更详细的病史资料显示,他童年时曾患类风湿性关节炎,20多岁时曾患无菌性脑膜炎。自身炎症性疾病的基因检查显示,NLRP3 基因发生了复合杂合突变,导致低温蛋白相关周期性发热综合征(CAPS)。该病例属于非典型 CAPS,表现为早发性进行性痴呆,没有反复发热或荨麻疹样疹子,而这些症状通常在这种疾病中出现。
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[Cryopyrin-associated periodic fever syndrome (CAPS) presenting as early-onset dementia, lacking typical recurrent fever or skin rash: a case report].

A 54-year-old man with a university degree was admitted to our hospital because of a two-year history of progressive dementia. He had familial sensorineural hearing loss and had been treated for epilepsy since his 30s. On admission, he showed severe dementia and parkinsonism without fever or skin rash. Systemic inflammation was evident, and the CSF cell count and IL-6 level were elevated to 53/μl and 307 ‍pg/ml, respectively. Brain MRI demonstrated diffuse brain atrophy. More detailed anamnesis revealed a history of rheumatoid arthritis in childhood and aseptic meningitis in his 20s. Genetic examination for autoinflammatory diseases demonstrated compound heterozygotic mutations in the NLRP3 gene, causing cryopyrin-associated periodic fever syndrome (CAPS). This case was atypical CAPS presenting as early-onset progressive dementia, without recurrent fever or urticaria-like eruption which are usually seen in this disease.

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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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