Young-onset frontotemporal dementia with FUS pathology. Issue 2 (11th December 2020)

• Record Type: Journal Article
• Authors: Gowell, Matthew; Baker, Ian; Ansorge, Olaf; Husain, Masud
• Is Part Of: Practical neurology. Volume 21:Issue 2(2021)
• Page Start: 149
• Page End: 152
• Publication Date: 2020-12-11
• Subjects: dementia -- neuropsychology -- histopathology -- behavioural disorder; Neurology -- Periodicals; 616.8005
• DOI: 10.1136/practneurol-2020-002730
• Languages: English
• ISSNs: 1474-7758

Abstract

Abstract : Frontotemporal dementia (FTD) is an uncommon cause of behavioural change in adults under the age of 50. A 44-year-old man presented with progressive neuropsychiatric disturbance characterised by social withdrawal, apathy, loss of empathy, motor stereotypies and hyperorality. Cognitive testing identified severe impairment, including executive dysfunction. MR scan of the brain showed bilateral symmetrical frontal atrophy. There was no relevant family history, and targeted genetic testing for FTD-associated variants in MAPT, GRN and C9orf72 genes proved negative. He became more withdrawn with disinhibited behaviour; his condition progressively worsened and he died 6 years later. The pathological diagnosis was frontotemporal lobar degeneration with fused-in-sarcoma (FUS) pathology, a rare sporadic cause of FTD, accounting for only 5%–10% of cases, its characteristic features including very young onset, motor stereotypies and hyperorality.