Volume 36, Issue 11 pp. 2361-2366
Case Series

Cardiac Myxoma: A Rare Case Series of 3 Patients and a Literature Review

Haiyan Wang MD

Corresponding Author

Haiyan Wang MD

Department of Ultrasound, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan, Shandong Province, China

Address correspondence to Haiyan Wang, MD, Department of Ultrasound, Shandong Provincial Qianfoshan Hospital, Shandong University, No. 16766 Jingshi Rd, 250014, Jinan, Shandong Province, China. E-mail: [email protected]Search for more papers by this author
Quan Li MD

Quan Li MD

Department of Cardiac Surgery, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan, Shandong Province, China

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Minghua Xue MS

Minghua Xue MS

Department of Ultrasound, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan, Shandong Province, China

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Pengzhan Zhao MS

Pengzhan Zhao MS

Department of Ultrasound, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan, Shandong Province, China

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Jing Cui MD

Jing Cui MD

Pathology, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan, Shandong Province, China

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First published: 27 May 2017
Citations: 23

This research was supported by the Projects of Medical and Health Technology Development Program in Shandong Province (2016WS0483).

Abstract

Myxoma is the most common tumor in the heart. A typical myxoma is relatively straightforward to diagnose. However, certain cardiac myxomas have rare features. We report three extremely rare cases of cardiac myxoma. One case involved a myxoma that originated from the annulus of the tricuspid after valvuloplasty, one case involved myxomas associated with left atrial thrombus and severe mitral stenosis, and the third case involved myxoma combined with severe calcification. All three cases were diagnosed by echocardiography and pathology. We also review clinical presentations and diagnostic characteristics of cardiac myxomas.

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