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Annals of Clinical and Analytical Medicine

E-ISSN: 2667-663X · Monthly · English

An unusual cause of chest pain: atrial myxoma: A Case Report

Cause of chest pain: atrial myxoma

Abstract

Myxomas are the most common primary tumors of the heart. It usually occurs in the left atrium and ventricle, and rarely in the right atrium.
A middle-age patient presented to our clinic with chest pain and difficulty in breathing. Patient had no previous cardiac history. Contrast-enhanced thorax computed tomography (CT) angiography showed a mass lesion in the right atrium and ventricle. Transthoracic echocardiography performed by the cardiologist of the patient revealed a 58 x12 mm mobile mass extending from the inferior vena cava (IVC) mouth to the top of the tricuspid valve. Transesophageal echocardiography (TEE) was recommended. Transesophageal echocardiography was performed. In the right atrium and in the right ventricle, a moving crescentshaped 12x15 mm lesion extending over the tricuspid valve stretching out to the inferior vena cava bifurcation from the IVC mouth with a crescent-shaped 200x58 mm moving lesion were observed. Histopathological examination of the operation performed by cardiovascular surgery was compatible with myxoma. Myxomas may be asymptomatic in the left atrium, reaching to very large dimensions and rarely present in the right atrium and valve involvement. Cardiac myxomas should be remembered as a rare cause in young patients who come to the emergency department with nonspecific symptoms such as chest pain and shortness of breath.

Keywords

anginamyxomaright atrium

Introduction

70-75% of cardiac tumors are benign. Myxomas are common in primary cardiac tumors and their incidence is between 30 and 50%.1 Approximately 85% of cardiac myxomas are found in the fossa ovalis in the left atrium; 18% are located in the right heart.2 Right atrial myxomas tend to be more solid and broad-based than left atrial myxomas. They sit on the atrial wall or septum with a larger base than the myxomas on the left.3 Diagnosis is made by echocardiography in almost all myxomas.4 Although myxomas mimic many cardiovascular diseases, doubt is the most important point for early diagnosis.5

Case Presentation

A middle-age patient presented to our clinic with chest pain and difficulty in breathing. The patient had no previous cardiac history. The patient stated that these complaints had not occurred before and that the patient had applied because of the occurrence and exacerbation of the last few days. There was no additional disease except hypertension. Physical examination revealed fever of 36.4 ° C; pulse 88 beats/minute; blood pressure was 150/90 mmHg and respiratory rate was 20 / minute. The patient had right apical 2/6 systolic murmur. Hepatosplenomegaly and venous fullness were not observed. Laboratory findings were normal. Electrocardiography revealed normal sinus rhythm. Contrast-enhanced thorax computed tomography (CT) angiography showed a mass lesion in the right atrium and ventricle (Figure 1 and Figure 2). Transthoracic echocardiography performed by the cardiologist of the patient revealed a 58 x12 mm mobile mass extending from the inferior vena cava (IVC) mouth to the top of the tricuspid valve. This mass lesion was thought to be a thrombus. The patient was then evaluated for cardiovascular surgery, and mass and thrombus could not be differentiated. Transesophageal echocardiography (TEE) was recommended. Transesophageal echocardiography was performed; in the right atrium and in the right ventricle, a moving, crescent-shaped 12x15 mm lesion extending over the tricuspid valve stretching out to the inferior vena cava bifurcation from the IVC mouth with a crescent-shaped 200x58 mm moving lesion were observed. This mass lesion was thought to be thrombus. Later, medical treatment was recommended by cardiovascular surgery and hospitalization was planned by the cardiology unit.
Subsequently, the patient was referred to cardiovascular surgery service due to suspicion of a mass lesion caused by the absence of regression in the thrombus. Histopathological examination of the operation performed by cardiovascular surgery was compatible with myxoma. After the operation, anticoagulant treatment was initiated and when the effective INR level was reached, the patient was healed and discharged. Echocardiography was normal in the outpatient follow-up and the patient was recommended to continue the outpatient follow-up.

Discussion

Myxoma is the most common benign cardiac tumor.1 Cardiac myxomas are rarely located in the right heart.2 Valve placement of tumors is rare.6-7 Although the mass was seen in both right atrium and ventricle, tricuspid valve involvement was present in our case and this is a rare condition. The clinic of the patient varies according to the size and location of myxoma.8 As it is seen in the literature, these cases will be asymptomatic or present non-specific symptoms such as hemodynamic disorders, peripheral, cerebral and coronary emboli, fever and fatigue, as well as mitral stenosis-like symptoms such as dyspnea, hemoptysis and chest pain. Meng et al. found that 4% of the cases were asymptomatic.9 Printer et al. in their study, presented only asymptomatic patients suspected of cardiac murmur.10 Our case was admitted to the emergency department with chest pain and dyspnea. Echocardiography plays an important role in the diagnosis, treatment, and follow-up of patients with myxoma. However, CT imaging used for differential diagnosis showed its importance once again in cases like ours where patients present with chest pain and thoracic CT angiography revealed mass lesion.11-12 The primary treatment approach in the treatment of myxoma is surgery. Life expectancy with surgery is close to perfect.13 In our case, we detected the mass by CT and tried to differentiate by transthoracic and transesophageal echocardiography in order to differentiate between thrombus and mass. Then surgical treatment of the patient was planned. Myxomas may be asymptomatic in the left atrium, reaching very large dimensions and rarely present in the right atrium and valve involvement. Cardiac myxomas should be remembered as a rare cause in young patients who come to the emergency department with nonspecific symptoms such as chest pain and shortness of breath.

Declarations

Animal and Human Rights Statement

All procedures performed in this study were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. No animal or human studies were carried out by the authors for this article.

Data Availability

The datasets used and/or analyzed during the current study are not publicly available due to patient privacy reasons but are available from the corresponding author on reasonable request.

Conflict of Interest

None of the authors received any type of financial support that could be considered potential conflict of interest regarding the manuscript or its submission.

Funding

None.

Acknowledgements

The authors appreciate kind support of Katip Çelebi University Atatürk Research and Training Hospital, Department of Emergency Medicine

References

  1. Braunwald E. Heart Disease: A Textbook of Cardiovascular Medicine. WB Saunders Company; 1984:1741-1755.
  2. Bhan A, Mehrotra R, Choudhary SK, et al. Surgical experience with intracardiac myxomas: long-term follow-up. Ann Thorac Surg. 1998;66(3):810-813. doi:10.1016/s0003-4975(98)00591-8
  3. Selvaraj A, Kumar R, Ravikumar E. Surgical management of right atrial myxomas: a 15-year experience with review of the literature. J Cardiovasc Surg (Torino). 1999;40:101-105.
  4. Jelic J, Milicić D, Alfirević I, et al. Cardiac myxoma: diagnostic approach, surgical treatment and follow-up: a twenty years experience. J Cardiovasc Surg (Torino). 1996;37(6 suppl 1):113-117.
  5. Pinede L, Duhaut P, Loire R. Clinical presentation of left atrial cardiac myxoma: a series of 112 consecutive cases. Medicine (Baltimore). 2001;80(3):159-172. doi:10.1097/00005792-200105000-00002
  6. Peters PJ, Reinhardt S. The echocardiographic evaluation of intracardiac masses: a review. J Am Soc Echocardiogr. 2006;19(2):230-240. doi:10.1016/j.echo.2005.10.015
  7. McAllister HA Jr, Fenoglio JJ Jr. Tumors of the Cardiovascular System. 2nd ed. Armed Forces Institute of Pathology; 1978:1-3. Atlas of Tumor Pathology; fascicle 15
  8. Duran NE, Özkan M. Left atrial myxoma with atypical localization. Turk Kardiyol Dern Ars. 2008;36(4):256-258.
  9. Meng Q, Lai H, Lima J, Tong W, Qian Y, Lai S. Echocardiographic and pathologic characteristics of primary cardiac tumors: a study of 149 cases. Int J Cardiol. 2002;84(1):69-75. doi:10.1016/s0167-5273(02)00136-5
  10. Yazici M, Norgaz T, Akdemir R, Albayrak S. Asymptomatic giant left atrial myxoma supplied from right coronary artery in a 65-year-old woman. Int J Cardiol. 2005;101(3):495-496. doi:10.1016/j.ijcard.2004.01.045
  11. Fyke FE III, Seward JB, Edwards WD, et al. Primary cardiac tumors: experience with 30 consecutive patients since the introduction of two-dimensional echocardiography. J Am Coll Cardiol. 1985;5(6):1465-1473.
  12. Ho VB, Hirsch JD. Left atrial myxoma. Mil Med. 2006;171.
  13. Keeling IM, Oberwalder P, Anelli-Monti M, et al. Cardiac myxomas: 24 years of experience in 49 patients. Eur J Cardiothorac Surg. 2002;22(6):971-977. doi:10.1016/s1010-7940(02)00592-4

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How to Cite This Article

Pınar Yeşim Akyol, Adem Çakır, Rezan Karaali, Zeynep Karakaya, Fatih Esad Topal. An unusual cause of chest pain: atrial myxoma: A Case Report. Ann Clin Anal Med 2020;11(6):646-648. doi:10.4328/ACAM.20127

Publication History

Received:
04.02.2020
Accepted:
24.02.2020
Published Online:
08.03.2020
Printed:
01.11.2020