- Case Report
- Open Access
Use of cardiovascular magnetic resonance in the evaluation of a giant right atrial appendage aneurysm: a case report and review of the literature
BMC Research Notes volume 10, Article number: 681 (2017)
Right atrial appendage aneurysms are rare entities that may have significant clinical consequences. When co-existing with atrial fibrillation, patients are at risk of developing pulmonary or paradoxical systemic emboli.
An elderly patient presented to medical attention with symptoms of acute diverticulitis. On abdominal computed tomography, a massively enlarged right atrial appendage aneurysm was discovered incidentally. The aneurysm caused marked compression of the right ventricle and contained an area of hypoenhancement concerning for an intraluminal thrombus. Gadolinium-enhanced cardiovascular magnetic resonance was performed and first-pass perfusion images demonstrated that the area of hypoenhancement was in fact poorly mixing blood. The patient was therefore managed medically.
Right atrial appendage aneurysms are infrequently encountered cardiac abnormalities. In the literature, surgery has been offered to patients who are young, symptomatic, or have evidence of thrombotic disease, although whether this practice pattern is associated with superior clinical outcomes is unclear. In the present case, gadolinium-enhanced cardiovascular magnetic resonance imaging was used to exclude the presence of intraluminal thrombus in an elderly patient, which helped orient the patient’s treating team towards medical—rather than surgical—therapy.
Right atrial appendage (RAA) aneurysms are abnormal dilatations of the RAA that are associated with dysplasia and fibrosis of the atrial tissue [1, 2]. They are rarely reported in the literature and are less frequently encountered compared to other cardiac aneurysms . A literature review published in 2014 found that the highest prevalence of RAA aneurysms was in the third decade of life, with cases noted from the perinatal period to 72 years of age . Since this review was published, however, there have been several additional pediatric cases reported [5,6,7,8,9].
RAA aneurysms are typically asymptomatic and are often discovered incidentally. The most common clinical findings in patients with symptomatic RAA aneurysms are persistent atrial tachyarrhythmia [5, 10,11,12,13,14] and dyspnea [6, 15]. Less frequently encountered findings are outlined in Table 1. While RAA aneurysms have been found in patients with atrial septal defects [7, 10, 12, 13, 16], ventricular septal defects, spontaneous pneumothoraces , left atrial appendage aneurysms, and tricuspid/mitral regurgitation , there is currently no clear etiological relationship between RAA aneurysms and these pathologies.
As RAA aneurysms are often diagnosed in the context of atrial fibrillation, the development of intraluminal thrombosis and subsequent pulmonary or paradoxical systemic embolism is of concern [17, 18]. Thrombus formation is as an indication in the literature for surgical resection of RAA aneurysms [17, 18]. However, the differentiation of an intraluminal thrombus from flow stasis is not always straightforward, especially when using echocardiography and contrast-enhanced computed tomography (CT) alone. We therefore present the use of cardiovascular magnetic resonance (CMR) to characterize a massive intraluminal hypodensity/filling defect in a patient with a RAA aneurysm found on CT.
An elderly patient between 50–70 years of age (details obscured to protect patient privacy) presented to medical attention with increasing left lower quadrant pain and nausea over 3 days. Relevant past medical history was significant for atrial fibrillation, diabetes mellitus, and hypertension. Family history, medications, and allergies were non-contributory.
Contrast-enhanced abdominal CT showed active sigmoid diverticulitis. The patient was put on bowel rest and was treated with intravenous hydration and antibiotics. Incidentally, on the superior aspect of the scan field, a massively enlarged RAA (10.0 × 6.0 cm) was noted causing marked mass effect on the right ventricle (RV) (Fig. 1). A large region of hypoenhancement (7.6 × 3.0 cm) was also identified at the tip of the RAA. Given the patient’s history of arrhythmia, the treating team was concerned about the presence of an intraluminal thrombus.
A cardiology consult was obtained and the patient was sent for echocardiography. Echocardiography similarly revealed an enlarged RAA that compressed the RV and contained an echogenic density at its tip. Right ventricular systolic pressure was 24 mmHg and the right ventricular inner diameter was mildly elevated at 3.6 cm. Doppler showed mild tricuspid and pulmonary valve insufficiency with normal flow rates. A normal left ventricular ejection fraction (55%) with concentric left ventricular hypertrophy was observed.
Cardiovascular magnetic resonance (CMR) (1.5 T, Philips Ingenia Imaging System®, Philips Healthcare®) imaging was subsequently performed. Balanced turbo field-echo (BTFE) short axis (sax) showed aneurysmal dilation of the RAA measuring 10.5 × 7.5 × 5.5 cm with a wide ostium of 3.6 × 3.6 cm. There was a lack of contractility of the aneurysm noted and evidence of significant compression of the right ventricular free wall during the cardiac cycle (see Fig. 2 or Additional file 1). Assessment of left and right global systolic functions using Simpson’s method in the short axis orientation revealed a normal left ventricular ejection fraction of 62% and a normal right ventricular ejection fraction of 57%.
Multiple CMR sequences showed a difference in signal between the blood pool contained within the RAA and the rest of the cardiac chambers (Fig. 3). Balanced fast field echo using SENSE technique (sB-FFE) showed that the contents of the RAA aneurysm was of lower signal intensity than the bright blood signal in the ventricles. T1-spin echo (T1-SE) images obtained without fat saturation demonstrated that the contents of the RAA aneurysm were of intermediate signal intensity as opposed to the dark blood signal in the RV. The signal intensity did not change with fat saturation. T2-weighted short-tau inversion relaxation (STIR) showed high signal intensity in the RAA in contrast to the dark blood pool in the ventricles. Finally, post-contrast sax images showed that the signal in RAA aneurysm was similar to that of the ventricular blood pools.
First-pass perfusion axial images were obtained following the administration of 25 mL of IV gadolinium contrast agent (Multihance®) (Additional file 2 and Fig. 4). The cine showed progressive mixing of the RAA aneurysm contents with contrast material until complete opacification. The signal abnormality on CT, echocardiography, and CMR was therefore concluded to have been caused by slow-mixing blood. Given the patient’s advanced age and the lack thrombotic disease, the patient was managed medically with anticoagulation.
RAA aneurysms are rare clinical entities. In the present case, gadolinium-enhanced CMR was used to exclude an aneurysmal thrombosis and orient the treating team towards medical management. To the best of the authors’ knowledge, this is first published case where CMR was used to direct therapy in such a context.
Echocardiography is the initial investigation of choice in the workup of cardiac abnormalities. It is inexpensive, widely available and minimally invasive. Echocardiography plays a particularly important role in the pediatric population, where the radiation exposure of CT scans and the long scan times of CMR are of particular concern . Indeed, agitated saline echocardiography has been used to differentiate RAA aneurysms from pericardial effusions in the neonate  and fetal ultrasound has been used to detect RAA aneurysms in the prenatal period [2, 9, 16]. Compared to CT and CMR, however, echocardiography has a poorer ability to differentiate RAA aneurysms from similarly-appearing anomalies  such as pericardial cysts , Ebstein’s anomaly , cor triatriatum , epicardial and pericardial fat lesions, and coronary aneurysms.
CT and CMR are both highly specific for the detection of RAA aneurysms . CT offers the benefit of a faster capture time, but it exposes patients to ionizing radiation and nephrotoxic contrast agents. Filling defects can be assessed on CT with delayed phase scanning 1–2 min after contrast administration, but this study is difficult to protocol in advance unless the operator is already aware of the defect.
CMR offers superior anatomical resolution and the ability to observe delayed blood mixing over time with cine imaging. CMR also has the ability to evaluate the function of the RV and to observe any mass effect exerted on the heart during the cardiac cycle. Presently, the use of CMR to assess RAA aneurysms in the literature has been limited; CMR was used in only 8 of 22 published English-language case reports (see Table 2 for a summary of published findings). This is likely due to the relatively recent emergence of the technology and its limited availability. Regardless, CMR can be invaluable in characterizing such cardiac abnormalities.
In present case, the treating team opted to pursue medical management once the area of hypoenhancement within the RAA aneurysm was characterized as slow flow by CMR. This conservative approach has been supported in the literature for patients who are asymptomatic and elderly [1, 6, 8]. Conversely, in patients who are younger, symptomatic, or who have evidence of thrombosis, surgical excision appears to be the preferred therapy [2, 5, 12,13,14,15]; a Cox-maze procedure may also be performed to treat concomitant arrhythmias [10, 14]. The rarity of RAA aneurysms makes it difficult to determine whether such an intervention confers a survival benefit, however .
The interaction of RAA aneurysms with other comorbidities merits mention. The patient in the present case also suffered from diverticulitis, a condition which may be treated medically or surgically. Such a scenario calls into question how other diseases should be managed in the context of RAA aneurysms, especially those that require surgery. Unfortunately, there is a paucity of data available in the literature to guide clinicians. The presence of a RAA aneurysm in and of itself does not appear to be a contraindication to surgery. However, if the aneurysm is large enough to affect cardiac output, contribute to outflow tract obstruction, or cause valvular regurgitation , then these comorbidities must be taken into consideration. For example, if the patient is preload dependent due to the impairment of ventricular function, this should be considered in the patient’s perioperative fluid management. If the patient presents in heart failure, inotropes and a monitored setting should be considered to maintain adequate post-operative tissue perfusion. In the present case, given the patient’s preserved biventricular function and minimal regurgitation, few peri-operative modifications would have been necessary. A pre-operative medical consultation would nonetheless have been recommended.
In conclusion, we present the use of CMR to characterize a giant RAA aneurysm containing an area of hypoenhancement on CT that was concerning for a massive thrombus. Multiplanar, multisequential gadolinium-enhanced CMR—including first-pass perfusion cine imaging—was used to characterize this area as slow flow and the patient was managed medically. Despite the rarity of this condition, future studies should be directed towards determining whether surgical management is of benefit compared to medical management.
acute marginal branch
balanced turbo field-echo
cardiac magnetic resonance
left ventricular ejection fraction
magnetic resonance imaging
right atrial appendage
right coronary artery
balanced fast field echo using SENSE technique
short-tau inversion recovery
T1 spin echo
Barberato SH, Barberato MF, Avila BM, Perretto S, Blume LD, Chamma Neto M. Aneurysm of the right atrial appendage. Arq Bras Cardiol. 2002;78(2):236–41.
Tejero-Hernandez MA, Espejo-Perez S, Suarez-de-Lezo-Cruz-Conde J. Congenital aneurysm of the right atrial appendage in a newborn: a rare anomaly. Rev Esp Cardiol (Engl Ed). 2012;65(1):99–100.
Aryal MR, Hakim FA, Ghimire S, et al. Left atrial appendage aneurysm: a systematic review of 82 cases. Echocardiography. 2014;31(10):1312–8.
Aryal MR, Hakim FA, Giri S, et al. Right atrial appendage aneurysm: a systematic review. Echocardiography. 2014;31(4):534–9.
Fang Z, Zeng L, Chen Y, Cui K. Paroxysmal atrial fibrillation originating from giant right atrial appendage aneurysm. Eur Heart J. 2015;36(46):3300.
Toufan M, Pourafkari L, Akbarzadeh F, Nader ND. A case of right atrial appendage aneurysm mimicking a pericardial cyst on echocardiogram. Echo Res Pract. 2014;1(1):K5–8.
Tunks RD, Malysz J, Clark JB. Neonatal management of a giant right atrial appendage aneurysm. Circulation. 2015;132(19):e226–8.
Xu YF, Yu F, Mao F, Ye XW, Ruan XZ, Zhang S. A case of right atrial appendage aneurysm in a 62-year-old man. Echocardiography. 2014;31(6):E191–4.
Cardiel Valiente L, Orden Rueda C, Ayerza Casas A, Palanca Arias D, Jimenez Montanes L. Right (atrial) appendage enlargement: prenatal diagnosis and postnatal follow up. An Pediatr (Barc). 2016;84(6):337–9.
Guaricci AI, Tarantini G, Basso C, et al. Images in cardiovascular medicine. Giant aneurysm of the right atrial appendage in a 39-year-old woman. Circulation. 2007;115(7):e194–6.
Sevimli S, Gundogdu F, Aksakal E, Arslan S, Gurlertop Y, Senocak H. A rare congenital anomaly: biatrial appendage aneurysm with atrial and ventricular septal defect. Echocardiography. 2007;24(9):987–90.
Corti F, Sciuchetti JF, Ferro O, Porta F, Redaelli M, Paolini G. Symptomatic right atrial appendance aneurysm: diagnosis and resection. J Cardiovasc Med. 2008;9(3):314–6.
Mizui S, Mori K, Kuroda Y. Ectopic atrial tachycardia due to aneurysm of the right atrial appendage. Cardiol Young. 2001;11(2):229–32.
Nakahara T, Minakata K, Yamazaki K, Funamoto M, Sakata R. Bilateral atrial appendage aneurysms associated with atrial fibrillation. Asian Cardiovasc Thorac Ann. 2014;22(3):347–9.
Gulati A, Gheta R, Chan CF, et al. Longitudinal follow-up of a right atrial appendage aneurysm by cardiac magnetic resonance imaging. Circulation. 2011;123(20):2289–91.
Ishii Y, Inamura N, Kayatani F. Congenital aneurysm of the right atrial appendage in a fetus. Pediatr Cardiol. 2012;33(7):1227–9.
Sondhi P, Wardhan H, Pandit N, Nath RK. A rare case of asymptomatic giant right atrial appendage aneurysm. J Am Coll Cardiol. 2013;61(1):104.
Contreras AE, Courtis JA, Brenna EJ, Amuchastegui M, Amuchastegui LM. Giant aneurysm of the right atrial appendage. Echocardiography. 2010;27(1):95–6.
Kurata A, Shishido-Hara Y, Hosaki A. Extremely enlarged right atrial appendage in paediatric idiopathic pulmonary hypertension. Acta Cardiol. 2010;65(4):483–5.
Yoon JW, Kim HJ, Lee SH, et al. A case of right atrial aneurysm incidentally found in old age. J Cardiovasc Ultrasound. 2009;17(3):96–8.
Duran NE, Erturk E, Gunduz S, Ozkan M. Aneurysm of the right atrial appendage in an elderly patient. Turk Kardiyol Dern Ars. 2009;37(2):122–4.
Le Ven F, Orhan E, Jobic Y. Aneurysm of right atrial appendage in a young patient. Arch Cardiovasc Dis. 2010;103(10):559–60.
LS contributed to manuscript preparation and revision. KS participated in case selection, preparation of CT and CMR images, and manuscript revision. EM participated in manuscript preparation and revision. FS, JF, and RC contributed to case selection, figure preparation, and manuscript revision. All authors take responsibility for their contributions. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Availability of data and materials
Consent for publication
The authors were unfortunately unable to contact the patient to obtain consent for publication of this case report despite numerous attempts (as verified by author KS). All scans have been anonymized and no clinical images (i.e. non-radiological) have been included. Only minimal patient data has been included to protect patient privacy.
Ethics approval and consent to participate
No funding was received for the draft of this manuscript.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Additional file 1. Balanced turbo field-echo cine in short axis view. The size and position of the right atrial appendage aneurysm is shown in relation to the right ventricle. Note how the right atrial appendage aneurysm compresses and deforms the right ventricle throughout the cardiac cycle.
Additional file 2. First pass perfusion cine of the right atrial appendage aneurysm in axial plane following the administration of IV gadolinium. Following the administration of 25 mL of IV gadolinium contrast agent (Multihance®), there is progressive and complete enhancement of the RAA aneurysm. This indicates that the area of hypoenhancement found on contrast-enhanced computed tomography was slow-flowing blood, rather than a thrombus.
About this article
Cite this article
Sivakumaran, L., Sayegh, K., Mehanna, E. et al. Use of cardiovascular magnetic resonance in the evaluation of a giant right atrial appendage aneurysm: a case report and review of the literature. BMC Res Notes 10, 681 (2017). https://doi.org/10.1186/s13104-017-3046-2
- Right atrial appendage aneurysm
- Cardiovascular magnetic resonance (CMR)
- Congenital heart anomaly