| Literature DB >> 31587935 |
Satoshi Bujo1, Eisuke Amiya2, Toshiya Kojima1, Shintaro Yamada1, Hisataka Maki1, Masato Ishizuka1, Masae Uehara1, Yumiko Hosoya3, Masaru Hatano3, Akatsuki Kubota4, Tatsushi Toda4, Issei Komuro1.
Abstract
We describe a case of anti-mitochondrial antibody-positive myositis associated with cardiovascular involvement. An electrophysiological study (EPS) showed binodal dysfunction, and cardiac magnetic resonance (CMR) imaging revealed left ventricular dysfunction with diffuse, patchy T2 high-intensity areas and late gadolinium enhancement indicative of inflammation and fibrosis. The left ventricular dysfunction was successfully treated with immunosuppressive therapy as documented by CMR. Persistence of conduction system dysfunction was confirmed by EPS, and a pacemaker was implanted. CMR and EPS concisely documented the variable cardiac response to treatment in anti-mitochondrial antibody-positive myositis. We demonstrate the utility of cardiac investigations in this rare disorder.Entities:
Year: 2019 PMID: 31587935 DOI: 10.1016/j.cjca.2019.07.002
Source DB: PubMed Journal: Can J Cardiol ISSN: 0828-282X Impact factor: 5.223