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Keeling, I.M., Oberwalder, P., Anelli-Monti, M., Schuchlenz, H., Demel, U., Tilz, G.P., Rehak, P. and Rigler, B. (2002) Cardiac Myxomas: 24 Years of Experience in 49 Patients. European Journal of Cardio-Thoracic Surgery, 22, 971-977.
https://doi.org/10.1016/S1010-7940(02)00592-4

has been cited by the following article:

• TITLE: Cardiac Myxoma: 10 Years Study of Presentations, Resection and Outcome

  AUTHORS: Vinod Bhan, Sri Satyavathi, Kanchumarti Sudhakar Rao, Velam Vanajakshamma

  KEYWORDS: Cardiac Myxoma, Dyspnea, Trans-Septal Approach

  JOURNAL NAME: World Journal of Cardiovascular Surgery, Vol.11 No.10, October 29, 2021

  ABSTRACT: Background: Cardiac myxoma is a very rare heart tumor which presents as life threatening mass in cardiac chamber. The tumor may present with vague symptoms which can lead to delay in diagnosis. Methods: 22 patients underwent complete excision of intracardiac myxoma between January 2011 and December 2020. Majority of the patients were females (60%) with mean age of 48.9 years who presented with symptoms of dyspnea on exertion. 3 patients had significant complications due to myxoma. 2 presenting with tumor embolism and limb ischemia while 1 patient presented with pulmonary edema. All patients were diagnosed by echocardiography which helped in evaluation of size and extent of tumor. Majority of patients underwent trans-septal biatrial approach for tumor excision. Results: 95% of patients survived the operation. The mean tumor size excised was 5.0 ± 1.6 cm in the largest diameter. 11 patients had sessile tumor while 1 patient had dumb bell tumor occupying both atria. 15 patients were surviving the operation while 2 deaths happened after 6 years of surgery. Conclusion: Cardiac myxomas are rare tumors which can cause severe systemic and cardiac symptoms in patients. Early diagnosis and immediate surgical management give excellent early and long-term results.