
Cardiac involvement with anti‐mitochondrial antibody‐positive myositis mimicking cardiac sarcoidosis
Author(s) -
Kadosaka Takahide,
Tsujinaga Shingo,
Iwano Hiroyuki,
Kamiya Kiwamu,
Nagai Azusa,
Mizuguchi Yoshifumi,
Motoi Ko,
Omote Kazunori,
Nagai Toshiyuki,
Yabe Ichiro,
Anzai Toshihisa
Publication year - 2020
Publication title -
esc heart failure
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.787
H-Index - 25
ISSN - 2055-5822
DOI - 10.1002/ehf2.12984
Subject(s) - medicine , myositis , myocarditis , cardiomyopathy , sarcoidosis , atrophy , cardiac sarcoidosis , cardiology , myopathy , heart failure , mitochondrial myopathy , pathology , mitochondrial dna , biochemistry , chemistry , gene
Anti‐mitochondrial antibody (AMA)‐positive myositis is an atypical inflammatory myopathy characterized by chronic progressive respiratory muscle weakness, muscular atrophy, and cardiac involvement. Arrhythmias, cardiomyopathy, and myocarditis have been reported as cardiac manifestations. Herein, we present the first report of a patient diagnosed with having AMA‐positive myositis with cardiac involvement mimicking cardiac sarcoidosis.