[Cryopyrin-associated periodic fever syndrome (CAPS) presenting as early-onset dementia, lacking typical recurrent fever or skin rash: a case report].
Tomone TanedaMizuki TakahashiMaiko UmedaYoshitaka UmedaMutsuo OyakeRyuta NishikomoriNobuya FujitaPublished in: Rinsho shinkeigaku = Clinical neurology (2024)
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.
Keyphrases
- early onset
- mild cognitive impairment
- late onset
- cognitive impairment
- rheumatoid arthritis
- multiple sclerosis
- single cell
- emergency department
- genome wide
- white matter
- healthcare
- magnetic resonance imaging
- resting state
- case report
- gene expression
- soft tissue
- computed tomography
- interstitial lung disease
- systemic sclerosis
- dna methylation
- drug induced
- disease activity
- systemic lupus erythematosus
- idiopathic pulmonary fibrosis
- brain injury
- acute care
- ankylosing spondylitis
- diffusion weighted imaging
- newly diagnosed