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Article type: Research Article
Authors: Abbate, Carloa; * | Trimarchi, Pietro D.b | Inglese, Silviaa | Damanti, Saraha; c | Dolci, Giulia A.M.d | Ciccone, Simonaa | Rossi, Paolo D.a | Mari, Danielaa; c | Arosio, Beatricea; c | Bagarolo, Renzob | Giunco, Fabriziob | Cesari, Matteoa; c
Affiliations: [a] Geriatric Unit, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, Milan, Italy | [b] Fondazione IRCCS Don Carlo Gnocchi, Milan, Italy | [c] Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy | [d] A.S.P. Pio Albergo Trivulzio, Milan, Italy
Correspondence: [*] Correspondence to: Carlo Abbate, Geriatric Unit, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, Via Alfonso Lamarmora 5, 20122 Milan, Italy. Tel.: +39 02 5503 3246; Fax: +39 02 50320735; E-mail: [email protected].
Abstract: Background:Alzheimer’s disease (AD) is a clinically heterogeneous disease. Multiple atypical syndromes, distinct from the usual amnesic phenotype, have been described. In this context, the existence of a right variant of AD (RAD), characterized by enduring visuospatial impairment associated with right-sided asymmetric brain damage, has been proposed. However, to date, this phenotype remains controversial. In particular, its peculiar characteristics and the independence from more prevalent cases (especially the posterior cortical atrophy syndrome) have to be demonstrated. Objective:To explore the existence of focal RAD on the basis of existing literature. Methods:We performed a literature search for the description of atypical AD presentations, potentially evoking cases of focal RAD. To be considered as affected by RAD, the described cases had to present: 1) well documented right-sided asymmetry at neuroimaging; 2) predominant cognitive deficits localizable on the right hemisphere; 3) no specific diagnosis of a known variant of AD. Results:Twenty-one cases were found in the literature, but some of them were subsequently excluded because some features of a different clinical syndrome were overlapped with the clinical features of RAD. Thirteen positive cases, three of them with pathologically confirmed AD, remained. A common right clinical-radiological syndrome, characterized by memory and visuospatial impairment with temporal and parietal involvement, consistently emerged. However, the heterogeneity among the reports prevented a definitive and univocal description of the syndrome. Conclusion:Even if sporadic observations strongly support the existence of a focal RAD, no definitive conclusions can still be drawn about it as an independent condition.
Keywords: Alzheimer’s disease, cognitive manifestations, left right asymmetry, right Alzheimer’s disease, right hemisphere, syndromic diversity, variant of Alzheimer’s disease, visuospatial ORCID: 0000-0002-0368-3834
DOI: 10.3233/JAD-190338
Journal: Journal of Alzheimer's Disease, vol. 71, no. 2, pp. 405-420, 2019
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