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Cerebral Amyloid Angiopathy or Frontotemporal Dementia? A Case Study | OMICS International| Abstract
ISSN: 2161-0460

Journal of Alzheimers Disease & Parkinsonism
Open Access

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  • Case Study   
  • J Alzheimers Dis Parkinsonism 2017, Vol 7(5): 373
  • DOI: 10.4172/2161-0460.1000373

Cerebral Amyloid Angiopathy or Frontotemporal Dementia? A Case Study

Thomas Benke1*, Christoph Scherfler1, Elfriede Karner1, Florian Dazinger2 and Evelin Donnemiller3
1Clinic of Neurology, Medical University of Innsbruck, Austria
2Department of Neuroradiology, Medical University of Innsbruck, Austria
3Department of Nuclear Medicine, Medical University of Innsbruck, Austria
*Corresponding Author : Thomas Benke, Klinik fur Neurologie, Medizinische Universitat Innsbruck, Anichstr. 35, A-6020 Innsbruck Osterreich, Austria, Tel: +43 512 504 81176, Email: thomas.benke@i-med.ac.at

Received Date: Aug 31, 2017 / Accepted Date: Sep 04, 2017 / Published Date: Sep 11, 2017

Abstract

A 67 year old patient developed progressive behavioral abnormalities and executive dysfunction corresponding to the diagnosis of behavioral variant of frontotemporal dementia (bvFTD). Unexpectedly, MRI showed multiple vascular ischemic and hemorrhagic lesions as typically found in sporadic cerebral amyloid angiopathy (SCAA). Based on clinical, laboratory and imaging findings the diagnosis of possible SCAA was made. SCAA may represent another important differential diagnosis among the various underlying disease pathologies of the bvFTD syndrome.

Keywords: Behavioral variant frontotemporal dementia; Cerebral amyloid angiopathy; Behavioral abnormalities; Dysexecutive syndrome

Citation: Benke T, Karner E, Scherfler C, Dazinger F, Donnemiller E (2017) Cerebral Amyloid Angiopathy or Frontotemporal Dementia? A Case Study. J Alzheimers Dis Parkinsonism 7: 373. Doi: 10.4172/2161-0460.1000373

Copyright: © 2017 Benke T, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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