- Case report
- Open Access
- Open Peer Review
Atypical atrial myxomas in two asymptomatic patients: a case report
© Charokopos et al; licensee BioMed Central Ltd. 2009
- Received: 24 July 2009
- Accepted: 8 September 2009
- Published: 8 September 2009
Atypical cardiac myxomas are a rare occurrence and may present with a variety of clinical manifestations depending on the morphology and location.
Two cases of cardiac myxomas atypically located in asymptomatic patients, diagnosed by transthoracic and transoesophageal echocardiography, are presented. In the first case a myxoma is located under the anterior mitral valve leaflet and in the second case a myxoma is located in the right atrium.
We emphasize the leading role of transthoracic and transoesophageal echocardiography in the diagnosis of intracavitary cardiac tumours.
- Mitral Valve
- Rheumatic Heart Disease
- Right Atrium
- Cardiac Myxoma
- Atrial Myxoma
Myxoma is the most common primary cardiac neoplasm and accounts for approximately one-half of all primary cardiac tumours. A left atrial myxoma was first described in a post-mortem examination in 1845. The specific signs and symptoms produced by a cardiac myxoma depend on its anatomic location. Approximately 75% of these tumours arise from the left atrium and 18% from the right atrium. The few remaining tumours originate from atypical sites such as left or right ventricle and valves [1–3].
We report two cases of atypical cardiac myxomas (originating from mitral valve and the right atrium), which were diagnosed by means of transthoracic (TTE) and transoesophageal echocardiography (TOE).
A 30- year-old man was admitted to our hospital with a history of hypertension. He had no history of cardiac symptoms, syncope or fever, and his past medical history was unremarkable.
The appearance of the LV mass was consistent with a myxoma arising from an atypical location. The patient was referred for surgical excision of the mass. Pathologic examination confirmed the diagnosis of myxoma. At 6-month follow-up, the patient was asymptomatic, and a TTE was within normal limits.
The mass was removed surgically and pathologic examination confirmed that it was a myxoma. A follow-up transthoracic echocardiogram was within normal limits. The patient was doing well 10 months after surgery.
Clinically, intracavitary tumours present with a dyad of clinical signs comprising obstruction and embolization . Dominating symptoms and signs relate to tumour location, which seems to be the main factor predicting obstructive sequelae and influencing embolic sites. Based on this concept, left atrial myxomas commonly cause mitral valve obstruction mimicking symptoms of rheumatic heart disease , while right-sided myxomas, being extremely rare, may present with nonspecific signs and symptoms, including right heart failure secondary to RV outflow tract obstruction . Although various clinical signs and symptoms produced by cardiac myxomas have been reported in the literature, asymptomatic giant cardiac myxomas of the right atrium, such as the one described in our second patient are very rare .
Echocardiography has made a profound impact on the diagnosis and management of cardiac myxomas. With M-mode and two-dimensional echocardiography the preoperative diagnosis of this pathology has increased to 90% . Even though TTE studies usually yield adequate images for the diagnosis of cardiac tumors, the use of TOE may offer valuable assistance in patients with poor acoustic windows by virtue of confirming tumor attachment site and dimensions, detecting other masses, and defining any obstruction to flow [2, 8]. With TOE we particularly evaluated the posterior left atrial wall, which often is not well displayed on TTE examination . Especially in case of left atrial myxomas associated with mitral stenosis, TOE can fairly easy discriminate an atrial thrombus from a myxoma.
Although echocardiography is the modality of choice in screening for cardiac masses, magnetic resonance imaging (MRI) and electron-beam computed tomography (EBCT) provide additional information about tissue characteristics and allow an excellent overview of the cardiac and paracardiac morphology. The advantage of these techniques is that they provide sectional views of cardiac and thoracic structures without superposition in any plane [1, 9–11].
About 75% of myxomas originate in the left atrium (LA) while 15-20% of them are located in the RA. The usual site of attachment is the area of the fossa ovalis in the LA . However, myxomas can be found in atypical locations, arising from the posterior or anterior LA wall or the atrial appendage . Rarely myxomas originate from the ventricle (3-4%) arising from the mitral valve. Atypical locations and multiple myxomas occur most frequently in cases of familial myxomatosis . Mitral valve myxomas may be localized to the anterior mitral leaflet, posterior mitral leaflet or mitral annulus. Usually the tumour is localized to the atrial-lower pressure side of the mitral valve [3, 12–14].
The treatment of choice for myxomas is surgical removal. Operative mortality ranges from 0% to 3% in multiple series. Recurrence rates are between 1% and 3% for sporadic myxomas, as a result of incomplete resection, versus 12% for familial myxomas .
In conclusion echocardiography is of primary importance, among the non-invasive diagnostic tools. It has facilitated the ante-mortem diagnosis of cardiac myxomas even if the patient is asymptomatic and the myxoma arises from an atypical location, as it was observed in our two patients.
Written informed consent was obtained at first visit from all patients for publication of this case report and all accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
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