Apollo Medicine

CASE REPORT
Year
: 2017  |  Volume : 14  |  Issue : 4  |  Page : 234--237

An intriguing case of rapidly progressive dementia: Creutzfeldt–Jakob Disease


Dinesh Chaudhari1, Pushpendra Nath Renjen2, Dhruv Zutshi3, Kamal Ahmad4, Abhas Kumar6 
1 DNB Internal Medicine, Institute of Neurosciences/Internal Medicine, Indraprastha Apollo Hospitals, New Delhi, India
2 Sr. Consultant Neurologist and Academic Coordinator, Institute of Neurosciences, Indraprastha Apollo Hospitals, New Delhi, India
3 Consultant Neurologist, Institute of Neurosciences, Indraprastha Apollo Hospitals, New Delhi, India
4 Consultant Physician, Institute of Neurosciences, Indraprastha Apollo Hospitals, New Delhi, India

Correspondence Address:
Pushpendra Nath Renjen
C-85, Anand Niketan, New Delhi - 110 021
India

Although no formal definition exists for what constitutes a rapidly progressive dementia (RPD), generally we use the term when dementia occurs in <1–2 years from illness onset, but more commonly over weeks to months. Prion diseases are the prototypical causes of RPD, but reversible causes of RPD might mimic prion disease and should always be considered in a differential diagnosis. We report the case of a 65-year-old male with progressive dementia and typical neurologic symptoms, myoclonic jerks, and magnetic resonance imaging findings of Creutzfeldt–Jakob disease (CJD). This case highlights the need for a high index of suspicion to diagnose CJD.


How to cite this article:
Chaudhari D, Renjen PN, Zutshi D, Ahmad K, Kumar A. An intriguing case of rapidly progressive dementia: Creutzfeldt–Jakob Disease.Apollo Med 2017;14:234-237


How to cite this URL:
Chaudhari D, Renjen PN, Zutshi D, Ahmad K, Kumar A. An intriguing case of rapidly progressive dementia: Creutzfeldt–Jakob Disease. Apollo Med [serial online] 2017 [cited 2023 Jan 27 ];14:234-237
Available from: https://apollomedicine.org/article.asp?issn=0976-0016;year=2017;volume=14;issue=4;spage=234;epage=237;aulast=Chaudhari;type=0