Cardiac Sarcoidosis: A Contemporary Concept of Forgotten Granulomatosis Publisher



Avagimyan A¹ ; Mkrtchyan L² ; Bairamyan T³ ; Jndoyan Z⁴ ; Navasardyan G⁵ ; Ginosyan K⁶ ; Aznauryan A⁷ ; Sahakyan K⁷ ; Ionov A⁸ ; Pavluchenko I⁹ ; Gogiashvili L¹⁰ ; Shafie D¹¹ ; Sarrafzadegan N¹² Show Affiliations
Source: ARYA Atherosclerosis Published:2023

Abstract

Sarcoidosis is a complex multisystem inflammatory granulomatous disease that can affect any organ, with a wide range of clinical presentations. A significant number of patients with systemic sarcoidosis may also have cardiac involvement. Clinical manifestations of cardiac sarcoidosis can include various rhythm and conduction disturbances, as well as heart failure. The structure of sarcoid granulomas is similar to that of tuberculous granulomas, but in contrast, they lack caseous necrosis. Tissue changes in sarcoidosis tissues depend on the stage of development of the disease, progressing from pathological process: macrophage-lymphocytic infiltration to epithelioid cell granuloma formation, and fibrosis. Granulomas can be found in any part of the myocardium, with the most common locations being the free wall of the left ventricle, the basal part of the interventricular septum, and the interatrial septum. Vasculopathy of the pulmonary circulation and coronary arteries is often observed. Advancements in diagnostic imaging techniques, such as computer tomography and magnetic resonance imaging, have facilitated the verification of cardiac sarcoidosis. This article presents an analysis of updated information on cardiac sarcoidosis by a multidisciplinary working group. © 2023, Isfahan University of Medical Sciences(IUMS). All rights reserved.