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Congenital complete absence of the left pericardium: a rare cause of chest pain or pseudo-right heart overload

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TLDR
Congenital defects of the pericardium are rare and poorly known cardiac malformations and are usually incidentally diagnosed.
Abstract
Background Congenital defects of the pericardium are rare and poorly known cardiac malformations. Most of them are left-sided and asymptomatic and are usually incidentally diagnosed. Aims To describe the clinical, electrocardiographic, and imaging features of total absence of the left pericardium. Methods and Results We report the cases of 3 patients who have been seen in our institution with a diagnosis of total congenital absence of the pericardium. All of them complained of precordial pain; one of them experienced disabling symptoms that justified surgical intervention. All of them had previously been suspected to have an atrial septal defect because of the echocardiographic appearance of right ventricular volume overload. Electrocardiogram, chest x-ray, echocardiography, and magnetic resonance imaging of the heart consistently showed remarkably similar features including leftward displacement, increased mobility, and interposition of lung tissue between the heart and other intrathoracic structures. Conclusion Congenital absence of the left pericardium should be known by clinicians as a possible differential diagnosis of chest pain or pseudo-right heart overload. Copyright © 2010 Wiley Periodicals, Inc.

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Citations
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Journal ArticleDOI

Multimodality Imaging for the Assessment of Pericardial Diseases

TL;DR: Multimodality imaging has significantly facilitated the diagnosis and long-term management of patients with pericardial diseases and the role of these imaging modalities in overall prognosis and prevention remains to be investigated.
Journal ArticleDOI

Congenital Absence of the Pericardium

TL;DR: The purpose of this review is to highlight the common clinical and multimodality imaging features associated with this anomaly and suggest a management algorithm.
Journal ArticleDOI

Congenital Abnormalities of the Pericardium

TL;DR: This work reviews the presentation, diagnosis, and management of congenital absence of the pericardium,pericardial cysts, and diverticula and a summary of multimodality imaging features is provided.
Journal ArticleDOI

Congenital absence of the pericardium and its mimics

TL;DR: Cases of pericardial absence are presented that show isolated right- and left-sided defects, as well as entities in the differential diagnosis, which may be isolated or associated with complex heart disease.
Journal ArticleDOI

Bronchogenic cyst associated with pericardial defect: Case report and review of the literature

TL;DR: The case of a 32-year-old man with a partial defect of the left pericardium and a bronchogenic cyst arising from the border of thepericardial defect is described.
References
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Journal ArticleDOI

Isolated congenital absence of the pericardium: clinical presentation, diagnosis, and management

TL;DR: Isolated CAP has a common presentation pattern with periodic stabbing chest pain mimicking coronary artery disease, and Symptomatic patients with the complete form may benefit from pericardioplasty.
Journal ArticleDOI

Echocardiography in congenital and acquired absence of the pericardium. An echocardiographic mimic of right ventricular volume overload.

M N Payvandi, +1 more
- 01 Jan 1976 - 
TL;DR: It is concluded that absence of the pericardium results in echocardiographic abnormalities which mimic those seen in right ventricular volume overload which may be due to altered cardiac position and motion within the thorax resulting from loss of normalPericardial restraint.
Journal ArticleDOI

Congenital absence of the pericardium: Echocardiography as a diagnostic tool

TL;DR: Between 1982 and 1992, 10 patients who underwent echocardiography at the Mayo Clinic were found to have congenital absence of the pericardium.
Journal ArticleDOI

Congenital defect of the pericardium

TL;DR: The morbid anatomy and histopathology is described as found at necropsy on a 7-year-old coloured girl who suffered from partial defect of the pericardium with prolapse and partial incarceration of the cardiac apex.
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