Informação da revista
Vol. 37. Núm. 9.
Páginas 793-795 (setembro 2018)
Partilhar
Partilhar
Baixar PDF
Mais opções do artigo
Vol. 37. Núm. 9.
Páginas 793-795 (setembro 2018)
Image in Cardiology
Open Access
Left pericardial defect: A rare cause of chest pain
Defeito do pericárdio esquerdo: uma causa rara de dor torácica
Visitas
4972
Ana Rita Pereiraa,
Autor para correspondência
pereira.anaritaf@gmail.com

Corresponding author.
, Ana Rita Almeidaa, Inês Cruza, Luís Rocha Lopesb,c,d, Isabel Joãoa, Hélder Pereiraa
a Cardiology Department, Hospital Garcia de Orta, Almada, Portugal
b Barts Heart Centre, Barts Health NHS Trust, London, United Kingdom
c Institute of Cardiovascular Science, University College London, London, United Kingdom
d Centro Cardiovascular, Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal
Este item recebeu

Under a Creative Commons license
Informação do artigo
Texto Completo
Baixar PDF
Estatísticas
Figuras (3)
Mostrar maisMostrar menos
Material adicional (1)
Texto Completo

Congenital pericardial defects are extremely rare with a reported incidence of <1 in 10000 and a male:female ratio of 3:1. Most patients are asymptomatic and diagnosis is usually incidental. Symptomatic patients present a range of non-specific symptoms, meaning that imaging is crucial for diagnosis.

A 46-year-old woman was referred to our department with symptoms of palpitations and atypical chest pain. Clinical examination found a palpable apical impulse on the midaxillary line. Electrocardiogram revealed sinus rhythm with a heart rate of 90 bpm, left anterior fascicular block and incomplete right bundle branch block. Chest X-ray (Figure 1) revealed levoposition and a “teardrop” appearance of the heart, superimposition of the right cardiac border over the spine, a prominent main pulmonary artery and a translucent area between the heart and the diaphragm.

Figure 1.

Chest X-ray showing marked levoposition and a “teardrop” appearance (dashed white line) of the cardiac silhouette, loss of right heart border due to superimposition over the spine (A), prominent main pulmonary artery (B) and translucent area between the diaphragm and the heart (C).

(0.28MB).

Unusual transthoracic echocardiographic windows were required, which showed paradoxical ventricular septal motion, cardiac hypermobility and apparent right ventricular dilation (Figure 2).

Figure 2.

Transthoracic echocardiogram images. (A) Parasternal long-axis view, bi-dimensional mode. (B) Parasternal long-axis view, M-mode, showing paradoxical septal motion. (C) Parasternal short-axis view of the base, showing apparent right ventricular dilation.

(0.15MB).

Systemic-to-pulmonary shunt, arrhythmogenic cardiomyopathy and congenital pericardial defect were considered as possible diagnoses.

As the echocardiographic images were suboptimal, cardiac magnetic resonance imaging (MRI) was performed (Figure 3), confirming leftward displacement of the heart (Figure 3A) and hypermobility (Video 1). Absence of left ventricular pericardium and pericardial fat (Figure 3B and C) and interposition of lung tissue between the great vessels (Figure 3D) were also observed. This last finding is considered a specific diagnostic sign (for some authors even a pathognomonic sign) of congenital pericardial defect.

Figure 3.

Cardiac MRI images. (A-D) Steady-state free precession images. (A) Axial image showing left and posterior heart displacement. (B) Axial image displaying non-visualization of the pericardium and pericardial fat around the left ventricle (between the white arrows). (C) Coronal image showing absence of the pericardium and pericardial fat around the left ventricle and great vessels (between the white arrows), with lung tissue interposition in the several recesses where the pericardium is usually found. (D) Axial image showing lung tissue in the aorto-pulmonary window (white arrow), which is considered a pathognomonic sign of this condition. (E) T1-weighted axial image with no abnormalities, particularly, fat tissue deposition. (F) Delayed gadolinium-enhanced axial image with no macroscopic areas of myocardial fibrosis/necrosis.

(0.35MB).

Therefore, our patient was diagnosed with complete defect of the left pericardium, which is the most common type described in the literature. As it is a form with good prognosis, no treatment was given and the patient was kept under regular follow-up.

Conflicts of interest

The authors have no conflicts of interest to declare.

Appendix A
Supplementary material

The following are the supplementary material to this article:

(3.6MB)

Copyright © 2018. Sociedade Portuguesa de Cardiologia
Baixar PDF
Idiomas
Revista Portuguesa de Cardiologia
Opções de artigo
Ferramentas
Material Suplementar
en pt

Are you a health professional able to prescribe or dispense drugs?

Você é um profissional de saúde habilitado a prescrever ou dispensar medicamentos

Ao assinalar que é «Profissional de Saúde», declara conhecer e aceitar que a responsável pelo tratamento dos dados pessoais dos utilizadores da página de internet da Revista Portuguesa de Cardiologia (RPC), é esta entidade, com sede no Campo Grande, n.º 28, 13.º, 1700-093 Lisboa, com os telefones 217 970 685 e 217 817 630, fax 217 931 095 e com o endereço de correio eletrónico revista@spc.pt. Declaro para todos os fins, que assumo inteira responsabilidade pela veracidade e exatidão da afirmação aqui fornecida.