| Literature DB >> 28219562 |
Sophie Georgin-Lavialle1, Aziz Guellich2, Jean-François Deux3, David Buob4, Thibaud Damy5.
Abstract
Light-chain-related amyloidosis is a systemic disease characterized by continuous accumulation of insoluble fibrillar proteins in different organs. Cardiac involvement is frequent in this condition. However, atypical presentations and unusual amyloid deposits localization may be encountered making the diagnosis challenging. We present here a case of a light-chain-related pericardial amyloidosis without evidence of myocardial involvement and emphasize the difficulty and importance of amyloidosis typing before starting treatment.Entities:
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Year: 2017 PMID: 28219562 DOI: 10.1016/j.athoracsur.2016.08.108
Source DB: PubMed Journal: Ann Thorac Surg ISSN: 0003-4975 Impact factor: 4.330