# A Rare Case of Isolated Cardiac Sarcoidosis With Negative Biopsy: Diagnosis by Clinical Criteria

**Authors:** Tiffany Le, John Dayco, Karthik Ramaseshan, Mariam Zunnu Rain, Luis C Afonso

PMC · DOI: 10.7759/cureus.52088 · Cureus · 2024-01-11

## TL;DR

This paper presents a rare case of cardiac sarcoidosis diagnosed using clinical and imaging criteria, even when a biopsy was negative.

## Contribution

The novelty lies in confirming cardiac sarcoidosis diagnosis without a positive biopsy, using clinical and imaging data.

## Key findings

- A case of cardiac sarcoidosis was diagnosed using clinical and imaging criteria despite a negative biopsy.
- The patient's cardiac function improved after treatment with corticosteroids, supporting the diagnosis.
- The case emphasizes the importance of clinical criteria in diagnosing rare conditions like cardiac sarcoidosis.

## Abstract

Cardiac sarcoidosis (CS) is a potentially life-threatening condition that can cause sudden, fatal conduction abnormalities, arrhythmias, and heart failure. The diagnosis of CS is challenging due to nonspecific symptoms and an unclear diagnostic criterion. Although biopsy is the gold standard method, the sensitivity of biopsy is low. About a portion of CS cases are detected through imaging. A unique aspect of our case is that our definitive diagnosis was made based on clinical and imaging criteria alone despite a negative biopsy. Our diagnosis was confirmed further on follow-up with improvement in cardiac function on imaging after a treatment course with corticosteroids. This case highlights the need to have a broad differential and more awareness of this rare etiology and the value of clinical criteria to make a definitive diagnosis.

## Linked entities

- **Diseases:** cardiac sarcoidosis (MONDO:0001707), heart failure (MONDO:0005252)

## Full-text entities

- **Diseases:** arrhythmias (MESH:D001145), CS (MESH:D012507), heart failure (MESH:D006333), conduction abnormalities (MESH:D054537)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10858628/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC10858628/full.md

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Source: https://tomesphere.com/paper/PMC10858628