# Complete Left-Sided Pericardial Congenital Absence

**Authors:** Petar Kalaydzhiev, Anelia Partenova, Radostina Ilieva, Kamelia Genova, Elena Kinova

PMC · DOI: 10.3390/reports7020048 · Reports · 2024-06-20

## TL;DR

This paper reports a rare case of complete left-sided pericardial absence in a 36-year-old male, highlighting the challenges in diagnosis and the importance of advanced imaging techniques.

## Contribution

The paper presents a detailed case of complete left-sided pericardial absence with insights into diagnostic challenges and imaging findings.

## Key findings

- ECG showed poor R-wave progression and repolarization abnormalities in leads V1–V4.
- Echocardiography revealed an unusual heart position and raised suspicion of a left-to-right shunt.
- Cardiac MRI confirmed complete left-sided pericardial absence.

## Abstract

Background: Congenital absence of pericardium is a rare cardiac disorder with a reported incidence of less than 1 in 10,000. Although most of the cases are of little clinical significance, some of them are associated with serious complications, including risk of herniation and strangulation or coronary artery compression. Detailed Case Description: We report a case of a 36-year-old male referred for routine cardiovascular examination. He had a medical history of a heart murmur since childhood. Electrocardiogram (ECG) revealed sinus rhythm, normal axis, poor R-wave progression in the precordial leads and repolarization abnormalities with negative T waves in leads V1–V4. On 2D transthoracic echocardiography (TTE), an unusual heart position was noted with poor image quality from the standard acoustic windows. The parasternal long axis view gave the impression of right ventricular dilatation. The findings raised the suspicion of left to right shunt and possible atrial septal defect. For further evaluation, the patient was referred for cardiac magnetic resonance which demonstrated complete left-sided absence of the pericardium. Discussion: Due to indistinct and atypical symptoms and lack of clinical awareness, pericardial congenital absence is frequently misdiagnosed. Patients may complain of atypical chest pain. Patient’s history and physical examination are often nonspecific. In cases with complete pericardial absence, ECG findings may include right axis deviation, right bundle block and sinus bradycardia. Echocardiography findings are also not characteristic, but some may raise the clinical suspicion of this diagnosis. The imaging modalities of choice are computed tomography and cardiac magnetic resonance. Treatment depends on the type of defect and clinical symptoms.

## Full-text entities

- **Diseases:** repolarization abnormalities (MESH:D000014), cardiac disorder (MESH:D006331), sinus bradycardia (MESH:D012804), Congenital absence of pericardium (MESH:D000757), heart murmur (MESH:D006337), herniation (MESH:D004677), chest pain (MESH:D002637), axis deviation (MESH:C566610), right ventricular dilatation (MESH:C566255), coronary artery compression (MESH:D003324), right bundle block (MESH:D002037), atrial septal defect (MESH:D006344)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12225519/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12225519/full.md

## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12225519/full.md

---
Source: https://tomesphere.com/paper/PMC12225519