Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000019.xml
Fortschr Neurol Psychiatr 2023; 91(06): 262-274
DOI: 10.1055/a-2055-4496
DOI: 10.1055/a-2055-4496
Fort- und Weiterbildung
Seltene Demenzerkrankungen: Frontotemporale Demenz
Rare Dementias: Frontotemporal Dementia
Abstract
Frontotemporal dementias (FTD) are among the rare dementias. Their symptomatology is - compared to the common Alzheimer’s disease - atypical, so that in many cases it takes a long time until a correct diagnosis is made. The following article gives an overview of the clinical symptoms, genetic and neuropathological basis, diagnostics and differential diagnostics and therapy.
Schlüsselwörter
frontotemporale Demenz - nicht-flüssige Aphasie - progrediente - semantische Demenz - primär progrediente AphasienKey words
frontotemporal dementia - non-fluent aphasia - progressive semantic dementia - primary progressive aphasiaPublication History
Article published online:
19 June 2023
© 2023. Thieme. All rights reserved.
Georg Thieme Verlag
Rüdigerstraße 14,70469 Stuttgart,
Germany
-
Literatur
- 1 Diehl-Schmid J. Frontotemporale lobäre Degenerationen. Neurotransmitter 2013; 24: 1-8
- 2 The Lund and Manchester Groups. Clinical and neuropathological criteria for frontotemporal dementia. J Neurol Neurosurg Psychiatry 1994; 57: 416-418
- 3 Rascovsky K, Hodges JR, Knopman D. et al. Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain 2011; 134: 2456-2477
- 4 Gorno-Tempini ML, Hillis AE, Weintraub S. et al. Classification of primary progressive aphasia and its variants. Neurology 2011; 76: 1006-1014
- 5 Kertesz A, Jesso S, Harciarek M. What is semantic dementia?. A cohort study of diagnostic features and clinical boundaries Arch Neurol 2010; 67: 483-489 2010.55
- 6 Josephs KA, Whitwell JL, Knopman DS. et al. Two distinct subtypes of right temporal variant frontotemporal dementia. Neurology 2009; 73: 1443-1450
- 7 Henry ML, Gorno-Tempini ML. The logopenic variant of primary progressive aphasia. Curr Opin Neurol 2010; 23: 633-637
- 8 Sajjadi S, Patterson K, Arnold R. et al. Primary progressive aphasia.A tale of two syndromes and the rest. Neurology 2012; 78: 1670-1677
- 9 Riedl L, Mackenzie IR, Förstl H. et al. Frontotemporal lobar degeneration: current perspectives. Neuropsychiatr Dis Treat 2014; 10: 297-310
- 10 Woolacott I, Rohrer J. The clinical spectrum of sporadic and familial form of frontotemporal dementia. J Neurochem 2016; 138
- 11 Greaves C, Rohrer J. An update on genetic frontotemporal dementia. J Neurol 2019; 266: 2075-2086
- 12 Diehl-Schmid J, Onur O, Kuhn J. et al. Imaging frontotemporal lobar degeneration. Curr Neurol Neurosci Rep 2014; 14: 489
- 13 Otto M, Feneberg E. Anderl-Straub S. Frontotemporale Demenz. Neuropathologie, Diagnostik und Therapie. Klinikarzt 2018; 47: 472-476
- 14 Ducharme S, Dols A, Laforce R. et al. Recommendations to distinguish behavioural variant frontotemporal dementia from psychiatric disorders. Brain 2020; 143: 1632-1650
- 15 Alberici A, Cottini E, Cosseddu M. et al. Suicide risk in frontotemporal lobe degeneration: to be considered, to be prevented. Alzheimer Dis Assoc Disord 2012; 26: 194-196
- 16 Ducharme S, Pearl-Dowler L, Gossink F. et al. The Frontotemporal Dementia versus Primary Psychiatric Disorder (FTD versus PPD) Checklist: A Bedside Clinical Tool to Identify Behavioral Variant FTD in Patients with Late-Onset Behavioral Changes. J Alzheimers Dis 2019; 67: 113-124
- 17 Valente E, Caramelli P, Gambogi L. et al. Phenocopy syndrome of behavioral variant frontotemporal dementia: a systematic review. Alzheimers Res Ther 2019; 11: 30
- 18 Gomez-Tortosa E, Serrano S, Toledo M. et al. Familial benign frontotemporal deterioration with C9ORF72 hexanucleotide expansion. Alzheimers Dement 2014; 10: S284-S289
- 19 Taylor K, Probst A, Miserez A. et al. Clinical course of neuropathologically confirmed frontal-variant Alzheimerʼs disease. Nat Clin Pract Neurol 2008; 4: 226-232
- 20 Levin J, Kurz A, Arzberger T. et al. Differenzialdiagnose und Therapie der atypischen Parkinson-Syndrome. Dtsch Ärztebl 2016; 113: 61-69
- 21 Respondek G, Krey L, Huber M. et al. Neuroprotektive Therapien bei Tauopathien. Nervenarzt 2021; 92: 1227-1238
- 22 Anderl-Straub S, Schuster J, Dorst J. et al. Amyotrophe Lateralsklerose und frontotemporale Demenz – auf dem Weg zu gemeinsamen genspezifischen Therapieansätzen. Nervenarzt 2021; 92: 1219-1226
- 23 Boxer A, Gold M, Feldman H. et al. New directions in clinical trials for frontotemporal lobar degeneration: Methods and outcome measure. Alzheimers Dement 2020; 16: 131-143
- 24 AWMF. S3-Leitlinie Demenzen. AWMF-Register-Nr. 038-013. 2016. Zugriff am 26. April 2022: https://www.awmf.org/leitlinien/detail/ll/038-013.html
- 25 Diehl-Schmid J, Knels C, Danek A. Chronic progressive aphasia. Nervenarzt 2009; 80: 1452-1461