Clinical Reasoning: A 69-Year-Old Man With Rapid Cognitive Decline and Abnormal Movements

The differentials for rapidly progressive dementia are broad, encompassing structural, infectious, inflammatory, neoplastic, and neurodegenerative etiologies. The presence of abnormal movements further complicates the diagnostic approach. We describe a 69-year-old man presenting with a diverse array of neurologic symptoms, starting with rapidly progressive cognitive impairment, later developing abnormal movements, sleep disruption, and constitutional symptoms. Despite extensive investigations and empirical treatment, the diagnosis remained elusive until postmortem evaluation. This case highlights the challenges inherent in neurologic diagnostic odysseys, offering insight into the diagnostic reasoning process and unveiling novel clinical findings that may aid earlier recognition of this rare disorder.

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Publication Details

Journal
Neurology
Published
2026-02-09
DOI
https://doi.org/10.1212/wnl.0000000000214686
Primary Topic
Cerebrovascular and genetic disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Clinical Reasoning: A 69-Year-Old Man With Rapid Cognitive Decline and Abnormal Movements

Gareth Zigui Lim, Yi-Roe Tan, Jonathan Yexian Lai, Javier Alegre‐Abarrategui et al.
Neurology
Cerebrovascular and genetic disorders
article

Clinical Reasoning: A 69-Year-Old Man With Rapid Cognitive Decline and Abnormal Movements

Gareth Zigui Lim, Yi-Roe Tan, Jonathan Yexian Lai, Javier Alegre‐Abarrategui, Tianrong Yeo, Leong Gen Yap, Adeline SL Ng, Jia Nee Foo
article en

Abstract

The differentials for rapidly progressive dementia are broad, encompassing structural, infectious, inflammatory, neoplastic, and neurodegenerative etiologies. The presence of abnormal movements further complicates the diagnostic approach. We describe a 69-year-old man presenting with a diverse array of neurologic symptoms, starting with rapidly progressive cognitive impairment, later developing abnormal movements, sleep disruption, and constitutional symptoms. Despite extensive investigations and empirical treatment, the diagnosis remained elusive until postmortem evaluation. This case highlights the challenges inherent in neurologic diagnostic odysseys, offering insight into the diagnostic reasoning process and unveiling novel clinical findings that may aid earlier recognition of this rare disorder.

NeurologyVol. 106(5)
Agency for Science, Technology and Research (SG), Nanyang Technological University (SG), Hammersmith Hospital (GB), Tan Tock Seng Hospital (SG), Duke-NUS Medical School (SG), National Neuroscience Institute (SG)
Imperial College London
Peace, Justice and strong institutions
Openalex Percentile: Top 63%
Cerebrovascular and genetic disorders
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