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[Senile systemic amyloidosis: definition, diagnosis, why thinking about?].

Authors :
Damy T
Mohty D
Deux JF
Rosso J
Benhaiem N
Lellouche N
Sabbah L
Guendouz S
Tissot CM
Rappeneau S
Pongas D
Bodez D
Krypciak S
Guellich A
Dubois-Randé JL
Hittinger L
Lefaucheur JP
Jaccard A
Planté-Bordeneuve V
Source :
Presse medicale (Paris, France : 1983) [Presse Med] 2013 Jun; Vol. 42 (6 Pt 1), pp. 1003-14. Date of Electronic Publication: 2013 May 11.
Publication Year :
2013

Abstract

Senile systemic amyloidosis (SSA) is characterized by infiltration of amyloid transthyretin fibrils in the myocardium. SSA occurs mainly (but not always) in elderly men. SSA leads to hypertrophic and/or restrictive cardiomyopathy complicated by conduction disturbances, atrial arrhythmia and systemic embolization (stroke…). That is why SSA needs a special care and to be diagnosed. Cardiac SSA diagnosis needs to exclude two other forms of cardiac amyloidosis: AL amyloidosis (light chain) and hereditary transthyretin amyloidosis (genetic testing). Scintigraphic 99mTc-DPD heart retention is observed in cardiac amyloidosis. DPD heart retention is more frequent in cardiac transthyretin amyloidosis than in cardiac AL amyloidosis. Specific treatments of cardiac TTR amyloidosis are in development.<br /> (Copyright © 2013. Published by Elsevier Masson SAS.)

Details

Language :
French
ISSN :
2213-0276
Volume :
42
Issue :
6 Pt 1
Database :
MEDLINE
Journal :
Presse medicale (Paris, France : 1983)
Publication Type :
Academic Journal
Accession number :
23669316
Full Text :
https://doi.org/10.1016/j.lpm.2013.03.004