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Senile cardiac amyloidosis: Clinical manifestations and non-invasive diagnostic approach
Author(s) -
Dimitrios Varvarousis,
Kali Polytarchou,
Nikolaos Th. Daskalopoulos,
Ioannis Mantas
Publication year - 2017
Publication title -
hellenic journal of cardiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.513
H-Index - 19
eISSN - 2241-5955
pISSN - 1109-9666
DOI - 10.1016/j.hjc.2017.01.006
Subject(s) - medicine , amyloidosis , cardiac amyloidosis , pathology , intensive care medicine
Cardiac amyloidosis (CA) refers to a rare metabolic storage disease with poor prognosis that relies on identification of the amyloid type. In our aging population, wild-type transthyretin amyloidosis (ATTRwt), also known as senile cardiac amyloidosis (SCA), is more common and must be differentiated from other amyloid types. We present a case of SCA diagnosed in a patient with signs and symptoms of congestive heart failure and discuss the clinical features, imaging study findings and the key “red flags” a clinician should evaluate to avoid underdiagnosis of SCA.

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