Search tips
Search criteria 


Logo of jcarultraJournal of Cardiovascular UltrasoundJournal of Cardiovascular UltrasoundAim and ScopeInstructions to AuthorArchive
J Cardiovasc Ultrasound. 2009 September; 17(3): 96–98.
Published online 2009 September 30. doi:  10.4250/jcu.2009.17.3.96
PMCID: PMC2889377

A Case of Right Atrial Aneurysm Incidentally Found in Old Age


Right atrial aneurysm is a rare abnormality of unknown origin. Approximately half of patients with right atrial aneurysm show no symptoms. Right atrial aneurysm is usually detected by chance at any time between fetal and adult life and can be associated with atrial arrhythmia and systemic embolism. The diagnosis of right atrial aneurysm can be established with echocardiography, computed tomography (CT) or magnetic resonance imaging (MRI). Because of thromboembolic risk, aneurysmectomy is usually recommended. We review the case report of a 69-year-wold woman with right atrial appendiceal aneurysm, whose diagnosis was established by echocardiography and CT angiography.

Keywords: Right atrial aneurysm, Transesophageal echocardiography, CT angiography


Right atrial aneurysm is a rare disease such that fewer than 60 cases have been reported worldwide.1) In South Korea, only three pediatric cases and no adult cases have been reported.2),3) Right atrial aneurysm predominantly results from a congenital extension of the right atrium; however, its cause has not yet been clarified. In about half of the reported cases, an abnormal finding on thoracic radiography was found incidentally while patients were asymptomatic. These cases can be diagnosed by echocardiography, CT and MRI. If no treatment is carried out, the risk of complications such as arrhythmia and thromboembolism will increase; therefore, medical or surgical treatment is recommended. The following describes the case report of an asymptomatic patient diagnosed with right atrial aneurysm at 69 years of age by echocardiography and CT angiography.


A 69-year-old normally healthy female visited a neighborhood hospital because of intermittent shoulder pain that had started several months earlier, and an abnormality was detected incidentally via thoracic radiography. She was asked to visit a larger hospital and ended up at our hospital. In terms of past history, she had been diagnosed with hypertension three years before and has since been taking antihypertensive medication. Further, her family history showed no specific findings. When she visited our hospital, her blood pressure was 130/70 mmHg, her pulse rate 75 beats per minute, and her body temperature 36.5[degree celsius]. An electrocardiogram showed 80 beats of normal sinus rhythm (Fig. 1); supraventricular arrhythmia was not found during 24-hour Holter monitoring, and no specific finding was found. However, a thoracic X-ray taken when the patient visited the hospital showed an outstanding heart shadow on the right lower cardiac border, but no abnormality finding was found in the lung parenchyma (Fig. 2). We performed transthoracic echocardiography (TTE) and transesophageal echocardiography (TEE) to evaluate the etiology of cardiomegaly. The size of the left atrium and of both ventricles of the heart were normal on the TTE, and the left ventricular ejection fraction (LVEF) was 72%. No abnormality was found in the structure and function of the valves, and abnormal wall motion was not observed. The TTE showed a cystic mass in the right atrial appendage without ultrasonic imaging. The mass was found to suppress the right ventricle during the diastolic phase (Fig. 3A); however, there was no significant limitation of blood flow to the right ventricle during the diastole phase. The TEE clearly showed the shape of the mass connected to the right atrium, which enabled the confirmed diagnosis of right atrial aneurysm (Fig. 3B). The TEE detected a spontaneous echo contrast inside the aneurysm, but no thrombus was found (Fig. 3C). On the CT angiogram, a 9.0 cm×5.2 cm×5.0 cm mass was found in the right atrial appendage, but stricture of the coronary arteries was not found (Fig. 4). The patient was asked to undergo right atrial aneurysm resection, but she denied the procedure and instead started anticoagulant therapy. The progress of her ambulatory care had been being followed up.

Fig. 1
ECG shows normal sinus rhythm. ECG: electrocardiography
Fig. 2
Cardiomegaly and right lower cardiac border bulging (arrow tip) was found at Chest PA. Lung parenchyma was normal. PA: posteroanterior.
Fig. 3
A: TTE shows aneurysm of the right atrial appendage producing compression of the right ventricle in diastole phase. B: TEE shows relation of right atrial appendiceal aneurysm and right atrium. C: In TEE, spontaneous echo contrast (arrow tip) swirling ...
Fig. 4
Cardiac coronary MDCT angiography shows 9.0 cm×5.2 cm×5.0 cm aneurysm of the right atrial appendage. MDCT: multi-detector computed tomography, RA: right atrium, RV: right ventricle, LV: left ventricle, AN: aneurysm.


Since the first report of right atrial aneurysm by Bailey in 1955,4) 60 cases have been reported worldwide. In South Korea, there have been three pediatric cases of right atrial aneurysm, with no adult case ever having been reported. The patients ranged in age from 32 weeks' gestation to 75 years at the time of diagnosis. Forty-eight percent of the reported patients had no symptoms, and other patients complained of arrhythmia, palpitations, shortness of breath, and fatigue. Normal sinus rhythm was observed on the electrocardiograms for 53% of the patients, and atrial fibrillation and flutter was observed in about 28%. In some cases, pre-excitation syndrome, junctional rhythm, heart block, supraventricular tachycardia, and so forth were reported,1) but the correlation between atrial aneurysm and arrhythmia has not yet been clarified. Most cases of asymptomatic right atrial aneurysm are discovered by chance as cardiomegaly with thoracic radiography. These cases can be easily diagnosed non-invasively by TTE, CT angiography, and so forth. If the result of diagnosis by the above methods is uncertain, TEE or cardiac MRI may be conducted. In this case, right atrial aneurysm was diagnosed by echocardiography, and CT angiography provided a certain diagnosis. Cardiac MRI was not performed because CT angiography is its equivalent in clarifying the structure of the coronary arteries, in relation to surrounding structures through three-dimensional reconstruction.5) Patients with right atrial aneurysm are known to have a high risk of supraventricular arrhythmia, stroke, and thromboembolisms including pulmonary thromboembolism; these risks have also been reported for left atrial aneurysm.6) Chatrath et al.4) reported that right atrial aneurysm might cause an extended tricuspid annulus due to an extended right atrium as well as tricuspid regurgitation. Therefore, anticoagulant therapy should be started upon diagnosis of right atrial aneurysm in order to prevent such complications. Ultimately, right atrial aneurysm resection should be performed. Since Morrow and Behrendt carried out the first right atrial aneurysm resection in 1968,7) surgical treatment has been reported several times to date. When cardiomegaly is found by chance on the thoracic radiogram of an asymptomatic patient, Ebstein's anomaly, pericardial effusion, pericardial cyst, tumor and so forth must be eliminated as possible causes.8) Whether to perform surgical treatment, for example, right atrial aneurysm resection, or to proceed non-surgically with continuous anticoagulant therapy in a patient with asymptomatic right atrial aneurysm is still considered controversial. However, surgical treatment should be preferentially recommended due to the possible risk of death owing to complications of arrhythmia and thromboembolism.9),10) This particular case is extremely rare, as it is the first instance of right atrial aneurysm found incidentally in old age in South Korea. Even though specific clinical symptoms and arrhythmia were not found, we recommended surgical treatment due to the risk of death from complications. However, she denied the treatment for the reasons of old age and a lack of symptoms. Currently, her progress is being observed with medication.


1. Verma G, Lanjewar CP, Kerkar PG. Idiopathic right atrial aneurysm. J Assoc Physicians India. 2007;55:590–592. [PubMed]
2. Yu YG, Kim JW, Chung SH, Park JJ, Yun TJ, Seo DM, Kim YH, Ko JK, Park IS, Kim JS. Surgical repair of the congenital aneurysm of the right atrium. Korean J Thorac Cardiovasc Surg. 2002;35:56–59.
3. Song JY, Sung JH, Lee JY, Kim SJ, Shim WS, Kim WH, Kim YM. A case of asymptomatic giant right atrial aneurysm. J Korean Pediatr Heart. 2004;7:138–141.
4. Chatrath R, Turek O, Quivers ES, Driscoll DJ, Edwards WD, Danielson GK. Asymptomatic giant right atrial aneurysm. Tex Heart Inst J. 2001;28:301–303. [PMC free article] [PubMed]
5. Lee SP, Kwon DA, Shin DH, Chung JW, Chang HJ, Kim KI, Cho YS, Youn TJ, Chung WY, Chae IH, Choi DJ, Kim CH. A case of congenital left atrial appendage aneurysm. J Kor Soc Echo. 2005;13:80–82.
6. Moon CS, Her MY, Seo WS, Jeong SR, Cho KH, Kim DK, Kim DI, Kim DS. A case of congenital left atrial appendage aneurysm. J Kor Soc Echo. 2002;10:55–59.
7. Morrow AG, Behrendt DM. Congenital aneurysm (diverticulum) of the right atrium. Clinical manifestations and results of the operative treatment. Circulation. 1968;38:124–128. [PubMed]
8. Beder SD, Nihill MR, McnaMara DG. Idiopathic dilation of the right atrium in a child. Am Heart J. 1982;103:134–137. [PubMed]
9. Barberato SH, Barberato MF, Avila BM, Perretto S, Blume Ld Ldo R, Chamma Neto M. Aneurysm of the right atrial appendage. Arq Bras Cardiol. 2002;78:236–241. [PubMed]
10. Zeebregts CJ, Hensens AG, Lacquet LK. Asymptomatic right atrial aneurysm : fotuitous finding and resection. Eur J Cardiothorac Surg. 1997;11:591–593. [PubMed]

Articles from Journal of Cardiovascular Ultrasound are provided here courtesy of Korean Society of Echocardiography