Myocarditis and endomyocardial biopsy: achieving consensus diagnosis on 100 cases
Zhen A Lu1, Mary Christine Aubry2, John T Fallon3
1Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Insights
Diagnosing myocarditis using histopathology remains challenging, even for experts. Achieving consensus is difficult, especially for borderline cases, highlighting the need for clearer diagnostic criteria.
Area of Science:
- Cardiovascular Pathology
- Histopathology
- Immunohistochemistry
Background:
- Myocarditis diagnosis relies on histopathology benchmarks like the Dallas Criteria and European Society of Cardiology criteria.
- The European Society of Cardiology criteria incorporate immunohistochemistry for CD3+ T cells and CD68+ macrophages.
- Consistency in applying these criteria for myocarditis diagnosis on endomyocardial biopsy (EMB) is not well understood.
Purpose of the Study:
- To assess the consistency and diagnostic confidence of international cardiovascular experts in diagnosing myocarditis from endomyocardial biopsies.
- To evaluate the challenges in diagnosing myocarditis, particularly borderline cases, using existing histopathological criteria.
Main Methods:
- 100 digitally scanned heart biopsy slides (myocarditis, non-myocarditis, borderline) were reviewed by eight blinded international experts.
- Experts rendered diagnoses and provided confidence scores without clinical history.
- Inter-expert agreement and consensus were analyzed after individual review and group discussion.
Main Results:
- Full initial agreement was observed in 37 cases, with moderate consensus in 35 cases.
- Consensus was reached on 90% of cases after discussion.
- Diagnostic confidence was highest for myocarditis, lowest for borderline cases, with significant differences across categories (P < 10^-50).
Conclusions:
- Histopathological diagnosis of myocarditis, especially with subtle inflammation, is challenging for experts.
- Borderline cases present significant difficulties in achieving diagnostic consensus.
- Improved, more granular criteria, clear immunohistochemistry integration, and refined nomenclature are needed for consistent myocarditis diagnosis.
Abstract:
The two histopathology benchmarks used to diagnose myocarditis are the Dallas Criteria, developed in 1984 and the European Society of Cardiology criteria, developed in 2013, which added immunohistochemistry for the detection of CD3+ T cells (lymphocytes) and CD68+ macrophages. Despite their near universal acceptance, the extent to which pathologists use these criteria or their own criteria to consistently render the diagnosis of myocarditis on endomyocardial biopsy (EMB) is unknown. We digitally scanned slides from 100 heart biopsies, including a trichrome stain and immunostaining, that were chosen as representative of myocarditis, non-myocarditis, and borderline myocarditis, as diagnosed per one institution's use of the Dallas Criteria. Eight blinded international cardiovascular experts were asked to render diagnoses and offer a confidence score on each case. No clinical histories were shared. There was full initial agreement across all experts on 37 cases (16 myocarditis and 21 non-myocarditis) and moderate consensus on 35 cases. After individual inquiries and group discussion, consensus was reached on 90 cases. Diagnostic confidence was highest among the myocarditis diagnoses, lowest for borderline cases, and significantly different between the three diagnostic categories (myocarditis, borderline myocarditis, non-myocarditis; P-value=8.49 × 10-57; ANOVA). Diagnosing myocarditis, particularly in cases with limited inflammation and injury, remains a challenge even for experts in the field. Intermediate cases, termed "borderline" in the Dallas Criteria, represent those for which consensus is particularly hard to achieve. To increase consistency for the histopathologic diagnosis of myocarditis, we will need more specifically defined criteria, more granular descriptions of positive and negative features, clarity on how to incorporate immunohistochemistry findings, and improved nomenclature.
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