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Diagnosis of cardiac sarcoidosis: histological evidence vs. imaging
Shinichi Kurashima1, Takeshi Kitai1, Andrew Xanthopoulos2
1Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, Suita, Japan.
Insights
Diagnosing cardiac sarcoidosis (CS) is challenging due to low biopsy detection rates. Current criteria, including Heart Rhythm Society and Japanese Circulation Society guidelines, offer different approaches, with advanced imaging aiding clinical diagnosis but requiring careful interpretation.
Area of Science:
- Cardiology
- Immunology
- Medical Imaging
Background:
- Cardiac sarcoidosis (CS) has a poor prognosis, necessitating early and accurate diagnosis.
- Endomyocardial biopsy has a low detection rate, complicating CS diagnosis.
- Current diagnostic criteria, including Heart Rhythm Society (HRS) and Japanese Circulation Society (JCS) guidelines, have limitations.
Purpose of the Study:
- To review the advantages and disadvantages of current CS diagnostic criteria.
- To discuss the role of advanced imaging in CS diagnosis.
- To highlight the significance of clinical manifestations and extracardiac findings in CS.
Main Methods:
- Comparison of HRS and JCS diagnostic guidelines for CS.
- Evaluation of multimodality imaging techniques (cardiac MRI, PET) in CS diagnosis.
- Analysis of clinical presentation and histological findings in CS.
Main Results:
- HRS criteria's reliance on histology can lead to missed diagnoses.
- JCS guidelines incorporate advanced imaging for clinical CS diagnosis.
- Clinical CS diagnosis shows promise but requires careful validation.
- Phenotyping based on clinical and extracardiac findings is crucial.
Conclusions:
- Accurate CS diagnosis remains challenging, balancing imaging and histology.
- Advanced imaging improves detection, but histological confirmation is often desired.
- Comprehensive phenotyping is essential for effective CS management.
Introduction:
The prognosis for cardiac sarcoidosis (CS) remains unfavorable. Although early and accurate diagnosis is crucial, the low detection rate of endomyocardial biopsy makes accurate diagnosis challenging.
Areas Covered:
The Heart Rhythm Society (HRS) consensus statement and the Japanese Circulation Society (JCS) guidelines are two major diagnostic criteria for the diagnosis of CS. While the requirement of positive histology for the diagnosis in the HRS criteria can result in overlooked cases, the JCS guidelines advocate for a group of 'clinical' diagnoses based on advanced imaging, including cardiovascular magnetic resonance and 18F-fluorodeoxyglucose positron emission tomography, which do not require histological evidence. Recent studies have supported the usefulness of clinical diagnosis of CS. However, other evidence suggests that clinical CS may sometimes be inaccurate. This article describes the advantages and disadvantages of the current diagnostic criteria for CS, and typical imaging and clinical courses.
Expert Opinion:
The diagnosis of clinical CS has been made possible by recent developments in multimodality imaging. However, it is still crucial to look for histological signs of sarcoidosis in other organs in addition to the endomyocardium. Additionally, phenotyping based on clinical manifestations such as heart failure, conduction abnormality or ventricular arrhythmia, and extracardiac abnormalities is clinically significant.
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