Cited by 119Viral Infections and Immunology ResearchSarcoidosis and Beryllium Toxicity ResearchVasculitis and related conditions

Idiopathic giant cell myocarditis and cardiac sarcoidosis

Blauwet, Lori A., Cooper, Leslie T.·2013·Heart Failure Reviews

Abstract

Idiopathic giant cell myocarditis (GCM) and cardiac sarcoidosis (CS) are rare disorders that cause cardiomyopathy, often with ventricular arrhythmias or heart block. Infection, autoimmune processes, and genetics have all been implicated in the pathogenesis of these diseases, but the etiology for both diseases is likely a complex multifactorial process. Both GCM and CS are generally progressive despite treatment with standard heart failure and arrhythmia therapies. Making the diagnosis of GCM or CS on initial clinical presentation is possible in only a small percentage of patients, so myocardial tissue diagnosis is required. The use of multiple noninvasive imaging modalities may aid in diagnosis and assessment of response to treatment. Establishing the diagnosis of GCM or CS early is crucial, as tailored immunosuppressive treatment may significantly alter the clinical course of these patients. The prognosis of patients with GCM is poor, while the prognosis for patients with CS varies according to degree of left ventricular dysfunction.

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Crossref · 10.1007/s10741-012-9358-3

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3 of 3 references verified0 citation errors · 0 not checkable

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  • Up to 20% of giant cell myocarditis cases are associated with existing autoimmune disorders such as inflammatory bowel disease, thyroiditis, and thymoma.

    “with up to 20% of giant cell myocarditis cases associated with existing autoimmune disorders such as inflammatory bowel disease, thyroiditis, and thymoma.”

    From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [29]

  • Giant cell myocarditis and eosinophilic necrotizing myocarditis are traditionally classified as autoimmune myocarditis due to their strong association with existing autoimmune conditions.

    “Giant cell myocarditis and eosinophilic necrotizing myocarditis are traditionally classified as autoimmune myocarditis due to their strong association with existing autoimmune conditions”

    From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [29]

  • Sarcoidosis is a systemic autoimmune syndrome characterized by nonnecrotizing granulomas in various organs including the lung and heart.

    “Sarcoidosis is a systemic autoimmune syndrome characterized by the formation of nonnecrotizing granulomas, a histological hallmark, found in various organs including the lung and heart.”

    From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [29]

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Authors
Blauwet, L. A., & Cooper, L. T.
Affiliations
Mayo Clinic (US)
Corresponding author
Blauwet, Lori A.
Venue
Heart Failure Reviews
Published
2012-10-31
Volume
18
Issue
6
Pages
733-746
ISSN
  • 1382-4147 (ISSN-L)
  • 1573-7322
OpenAlex
W2023589834
Cited by
119
References
3
Citations by year
2026: 6 · 2025: 7 · 2024: 10 · 2023: 11 · 2022: 10 · 2021: 14 · 2020: 9 · 2019: 8 · 2018: 7 · 2017: 10 · 2016: 11 · 2015: 9 · 2014: 7
FWCI
3.25
Type
journal article
Language
en
Open access
closed
Locations
  • Heart Failure Reviews (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Viral Infections and Immunology Research
  • Health Sciences › Medicine › Physiology › Sarcoidosis and Beryllium Toxicity Research
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Vasculitis and related conditions
Keywords
cardiac sarcoidosis, cardiomyopathy, ventricular arrhythmias, atrioventricular block, pathogenesis, noninvasive cardiac imaging, immunosuppressive therapy, prognosis, left ventricular dysfunction
MeSH terms
Cardiac Conduction System Disease, Arrhythmias, Cardiac, Biopsy, Needle, Contrast Media, Female, Heart Conduction System, Humans, Immunohistochemistry, Immunotherapy, Male, Cardiomyopathies, Myocarditis, Prognosis, Radiographic Image Enhancement, Sarcoidosis, Tomography, X-Ray Computed, Echocardiography, Doppler, Giant Cells, Magnetic Resonance Imaging, Cine, Rare Diseases, Positron-Emission Tomography, Brugada Syndrome, Multimodal Imaging

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