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      Myocardial Involvement in Patients With Histologically Diagnosed Cardiac Sarcoidosis: A Systematic Review and Meta‐Analysis of Gross Pathological Images From Autopsy or Cardiac Transplantation Cases

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          Abstract

          Background

          In patients with suspected cardiac sarcoidosis, late gadolinium enhancement on cardiovascular magnetic resonance imaging and/or 18F‐fluorodeoxyglucose uptake on positron emission tomography are often used to reach a clinical diagnosis of cardiac sarcoidosis. On the basis of data from the imaging literature of clinical cardiac sarcoidosis, no specific features of myocardial involvement are regarded as pathognomonic for cardiac sarcoidosis. Thus, a diagnosis of cardiac sarcoidosis is challenging to make. There has been no systematic analysis of histologically diagnosed cardiac sarcoidosis for patterns of myocardial involvement. We hypothesized that certain patterns of myocardial involvement are more frequent in histologically diagnosed cardiac sarcoidosis.

          Methods and Results

          We performed a systematic review and meta‐analysis of gross pathological images from the published literature of patients with histologically diagnosed cardiac sarcoidosis who underwent autopsy or cardiac transplantation. Thirty‐three eligible articles provided images of 49 unique hearts. Analysis of these hearts revealed certain features of myocardial involvement in >90% of cases: left ventricular (LV) subepicardial, LV multifocal, septal, and right ventricular free wall involvement. In contrast, other patterns were seen in 0% to 6% of cases: absence of gross LV myocardial involvement, isolated LV midmyocardial involvement, isolated LV subendocardial involvement, isolated LV transmural involvement, absence of septal involvement, or isolated involvement of only one LV level.

          Conclusions

          In this systematic review and meta‐analysis of histologically diagnosed cardiac sarcoidosis, we identified certain features of myocardial involvement that occurred frequently and others that occurred rarely or never. These patterns could aid the interpretation of cardiovascular magnetic resonance imaging and positron emission tomography imaging and improve the diagnosis and the prognostication of patients with suspected cardiac sarcoidosis.

          Abstract

          See Editorial Patel et al

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          Most cited references48

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          Systematic review of patients presenting with suspected myocardial infarction and nonobstructive coronary arteries.

          Myocardial infarction with nonobstructive coronary arteries (MINOCA) is a puzzling clinical entity with no previous evaluation of the literature. This systematic review aims to (1) quantify the prevalence, risk factors, and 12-month prognosis in patients with MINOCA, and (2) evaluate potential pathophysiological mechanisms underlying this disorder.
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            The WASOG Sarcoidosis Organ Assessment Instrument: An update of a previous clinical tool.

            A Case Control Etiology of Sarcoidosis Study (ACCESS) sarcoidosis organ assessment instrument has been used for more than a decade to establish uniform standards for the probability of sarcoidosis organ involvement. The ACCESS instrument has become increasingly outdated as new technologies have been developed. Furthermore, the ACCESS instrument failed to address all possible organs involved with sarcoidosis. For these reasons, the World Association of Sarcoidosis and Other Granulomatous Diseases (WASOG) developed a new sarcoidosis organ assessment instrument.
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              Fourth Universal Definition of Myocardial Infarction (2018)

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                Author and article information

                Contributors
                cshenoy@umn.edu
                Journal
                J Am Heart Assoc
                J Am Heart Assoc
                10.1002/(ISSN)2047-9980
                JAH3
                ahaoa
                Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
                John Wiley and Sons Inc. (Hoboken )
                2047-9980
                09 May 2019
                21 May 2019
                : 8
                : 10 ( doiID: 10.1002/jah3.2019.8.issue-10 )
                : e011253
                Affiliations
                [ 1 ] Cardiovascular Division Department of Medicine University of Minnesota Medical School Minneapolis MN
                [ 2 ] Section of Cardiology Department of Medicine University of Illinois at Chicago Chicago IL
                Author notes
                [*] [* ] Correspondence to: Chetan Shenoy, MBBS, University of Minnesota Medical Center, 420 Delaware St SE, MMC 508, Minneapolis, MN 55455. E‐mail: cshenoy@ 123456umn.edu
                Article
                JAH34071
                10.1161/JAHA.118.011253
                6585321
                31070111
                ca5346d4-b0da-4219-95b4-6ddab2adf3be
                © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 22 October 2018
                : 08 February 2019
                Page count
                Figures: 2, Tables: 4, Pages: 11, Words: 7840
                Categories
                Systematic Review and Meta‐analysis
                Systematic Review and Meta‐analysis
                Custom metadata
                2.0
                jah34071
                21 May 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.3 mode:remove_FC converted:23.05.2019

                Cardiovascular Medicine
                autopsy,cardiac sarcoidosis,cardiac transplantation,late gadolinium enhancement,myocardial structure,phenotype,prognosis,magnetic resonance imaging (mri),nuclear cardiology and pet,diagnostic testing,cardiomyopathy

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