Article

lock Open Access lock Peer-Reviewed

5

Views

CASE REPORT

Congenital Aneurysm of the Right Atrium: Two Cases Report

Halyna MeloI; Fernando MoraesI; Cleusa LapaI; Carlos R. MoraesI

DOI: 10.21470/1678-9741-2018-0047

INTRODUCTION

Congenital aneurysm or enlargement of the right atrium is a rare condition. It was firstly described and surgically corrected by Bailey[1] in 1955. In an extensive survey of the international literature from 1955 to 1988, Binder et al.[2] found 60 reported cases of right atrial aneurysm from which only 17 (28%) had been submitted to surgical treatment. Subsequently, sporadic cases have been described, including one of our experience[3-6]. In this article, we not only present another case, but probably more relevant, we describe the late results (17 years) of the surgery in the previously reported child.

CASES REPORT

Case 1 - A 14-months-old female patient was submitted to surgical excision of a right atrial aneurysm on March 30, 1999[3]. The diagnosis of congenital heart disease had been suspected by ultrasonography during fetal life. She was admitted to the emergency room of our institution presenting a paroxysmal supraventricular tachycardia which subsided with digoxin. Subsequently, she presented several episodes of arrhythmia. Physical examination was normal. Chest X-rays showed marked cardiomegaly. The electrocardiogram was normal. Echocardiogram demonstrated a massively dilated right atrium without any intracardiac abnormalities. Cineangiography confirmed the presence of a large aneurysm on the right atrium. Surgery was performed through a median sternotomy and normothermic cardiopulmonary bypass. The entire right atrium body was aneurismatic, but the atrial appendage was normal. The aneurysm was resected as much as necessary to simulate a normal-sized right atrium. The resected tissue measured 11 x 6 cm. The remaining right atrium was closed with a continuous 6-0 Prolene suture. The postoperative course was uneventful. She is now a 19-years-old health woman who had a normal pregnancy a year ago bearing a normal child. No episode of arrhythmia has occurred. Chest X-rays (Figure 1A), electrocardiogram, and echocardiogram are normal.

Fig. 1 - Chest X- rays of cases 1 and 2. Case 1: (a) Normal post-operative chest X-ray 17 years after surgery. Case 2: (b) Pre-operative chest X-ray showing marked cardiomegaly. (c) Normal post-operative chest X-ray.

Case 2 - A 14-years-old male patient who had been diagnosed intra-uterus with congenital aneurysm of the right atrium was referred to our institution for surgical treatment. He had symptoms of frequent palpitations. Physical examination was normal, except for a systolic murmur grade 3/6 heard at the tricuspid area. The electrocardiogram was normal. The chest X-ray showed enlargement of the cardiac area (Figure 1B). Echocardiogram revealed aneurysmal dilatation of the right atrium and moderate tricuspid regurgitation. On November 24th, 2016, the patient underwent surgical correction (Figure 2). Under conventional cardiopulmonary bypass, the right atrial aneurysm was resected. The tricuspid valve was normal, but the annulus was dilated and a ring annuloplasty was performed. The postoperative course was uneventful. Chest X-ray (Figure 1C) and echocardiogram are normal.

Fig. 2 - Intraoperative photographs of case 2. (a) View after the median sternotomy. (b) After establishment of extracorporeal circulation, the aneurysm sac is empty. (c) The resected right atrial tissue. (d) Heart after correction.

DISCUSSION

Congenital aneurysm of the right atrium also called idiopathic dilatation or congenital enlargement of the right atrium is rare. In our institution, over a period of 30 years (1987-2017), during which more than 23.000 cardiac operations have been performed, we have seen only 2 cases of such anomaly.

Right atrial aneurysms have been documented from neonatal to adult life[2]. In our cases, the suspicion of a cardiac anomaly was made during ultrasonography at gestation. Patients with right atrial aneurysms may be asymptomatic, but more frequently, as in our 2 children, they present supraventricular arrhythmias. This is probably the result of severe atrial dilatation since patients regained normal sinus rhythm after surgical removal of the aneurysm. Another possible complication is the formation of mural thrombus in the right atrium[2]. Massive dilatation of the right atrium may be associated with tricuspid annular dilatation and regurgitation requiring tricuspid annuloplasty. It did occur in our second patient.

In asymptomatic individuals, the diagnosis is suspected by the presence of cardiomegaly on chest radiography. Echocardiography may be the preferred method of diagnosis excluding other conditions such Ebstein's anomaly, pericardial effusion, pericardial cysts, and tumors. In a few cases, computed tomography, magnetic resonance imaging, and selective cineangiocardiography may be used to establish definitive diagnosis.

The analyses of the literature show that there is no unified opinion about the treatment of patients with aneurysm of the right atrium. Patients with arrhythmia have been treated surgically. Conservative approach is suggested to asymptomatic patients diagnosed with mild or moderate dilatation. We have advocated surgical treatment to all patients to prevent further dilatation of the right atrium and to avoid unexpected life-threatening complications. Moreover, the procedure has a low surgical risk[3] and the late results of surgery observed in our first patient, 17 years after operation, suggest that resection of the right atrial aneurysm is a curative procedure.

REFERENCES

1. Bailey CP. Surgery of the heart. Philadelphia: Lea and Febiger;1955. p.413-20.

2. Binder TM, Rosenhek R, Frank H, Gwechenberger M, Maurer G,Baumgartner H. Congenital malformations of the right atrium and the coronarysinus: an analysis based on 103 cases reported in the literature and twoadditional cases. Chest. 2000;117(6):1740-8.

3. Moraes F, Santos CL, Lira V, Moraes CR. Congenital aneurysm of theright atrium. Eur J Cardiothorac Surg. 2001;19(6):943-4.

4. Chatrath R, Turek O, Quivers ES, Driscoll DJ, Edwards WD, DanielsonGK. Asymptomatic giant right atrial aneurysm. Texas Heart Inst J.2001;28(4):301-3.

5. Mascio CE, Burkhast HM, Fagan T, Ge S, Behrendt DM. Neonatal rightatrial aneurysm. Ann Thorac Surg. 2005;80(6):2382.

6. Jonavicius K, Lipnevicius A, Sudikiene R, Zurauskas E, LebetkeviciusV, Tarutis V. Surgical repair of a giant congenital right atrial aneurysm: acase report. J Cardiothorac Surg. 2015;10:72.

No financial support.
No conflict of interest.

Authors' roles & responsibilities

HM Substantial contributions to the conception of the work; the acquisition and interpretation of data of the work; furthermore, agreement to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved; final approval of the version to be published

FMN Substantial contributions to the conception of the work; the analysis and interpretation of data for the work; final approval of the version to be published

CL Agreement to be accountable for all aspects of the work in ensuring that questions related to the accuracy and integrity of any part of the work are appropriately investigated and resolved; final approval of the version to be published

CRM Drafting the work and revising it critically for important intellectual content; final approval of the version to be published

Article receive on Sunday, February 18, 2018

CCBY All scientific articles published at rbccv.org.br are licensed under a Creative Commons license

Indexes

All rights reserved 2017 / © 2019 Brazilian Society of Cardiovascular Surgery DEVELOPMENT BY