Hostname: page-component-78c5997874-ndw9j Total loading time: 0 Render date: 2024-11-17T17:27:37.155Z Has data issue: false hasContentIssue false
  • English
  • Français

Familial atrial myxoma

Published online by Cambridge University Press:  18 August 2008

Pin Sun  and
Zhi-Bin Wang
Pin Sun*
Affiliation:
Department of Cardiac Ultrasound, Affiliated Hospital of Medical College, Qingdao University. Qingdao City, Peoples Republic of China
Zhi-Bin Wang
Affiliation:
Department of Cardiac Ultrasound, Affiliated Hospital of Medical College, Qingdao University. Qingdao City, Peoples Republic of China
*
Correspondence to: Pin Sun, Department of Cardiac Ultrasound, Affiliated Hospital of Medical College, Qingdao University. 16 Jiangsu Road, Qingdao City 266003, P. R. China. Tel: 86 532 8584 8885; Fax: 86 532 8291 1999; E-mail: [email protected]
Get access Rights & Permissions [Opens in a new window]

Abstract

The familial variant of cardiac myxoma is known to be an autosomally dominant disease. Early diagnosis, and removal of the tumours, are of great importance. In this regard, echocardiography is considered the simplest and most reliable diagnostic method. We report our experience with echocardiographic diagnosis of a family with atrial myxomas.

Keywords

Hereditaryatrial occupying lesionechocardiography
Type
Brief Report
Information
Cardiology in the Young , Volume 18 , Issue 5 , October 2008 , pp. 525 - 527
Copyright
Copyright © Cambridge University Press 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Gavrielatos, G, Letsas, KP, Pappas, LK, Dedeilias, P, Sioras, E, Kardaras, F. Large left atrial myxoma presented as fever of unknown origin: a challenging diagnosis and a review of the literature. Cardiovasc Pathol 2007; 16: 365–367.CrossRefGoogle Scholar
2. Meng, Q, Lai, H, Lima, J, Tong, W, Quian, Y, Lai, S. Echocardiographic and pathologic characteristics of primary cardiac tumors: a study of 149 cases. Int J Cardiol 2002; 84: 69–75.CrossRefGoogle ScholarPubMed
3. Rogov, KA, Sheremet’eva, GF, Nechaenko, MA. Family myxoma of the heart with metachronic multiple growth. Arkh Patol 2004; 66: 41–44.Google Scholar
4. Alter, P, Grimm, W, Rominger, MB, et al. Right ventricular cardiac myxoma. Diagnostic usefulness of cardiac magnetic resonance imaging. Herz 2005; 30: 663–667.Google Scholar
5. Grebenc, ML, Rosado-de-Christenson, ML, Green, CE, Burke, AP, Galvin, JR. Cardiac myxoma: imaging features in 83 patients. Radiographics 2002; 22: 673–689.CrossRefGoogle ScholarPubMed
6. Casey, M, Mah, C, Merliss, AD, et al. Identification of a novel genetic locus for familial cardiac myxomas and Carney complex. Circulation 1998; 98: 2560–2566.Google Scholar
7. Basson, CT, MacRae, CA, Korf, B, Merliss, A. Genetic heterogeneity of familial atrial myxoma syndromes (Carney complex). Am J Cardiol 1997; 79: 994–995.CrossRefGoogle ScholarPubMed
8. Percell, RL, Henning, RJ, Siddique Patel, M. Atrial myxoma: case report and a review of the literature. Heart Dis 2003; 5: 224–230.Google Scholar
9. Kirklin, JW. The future of cardiac surgery. Heart Dis Stroke 1993; 2: 361–364.Google Scholar
10. Stratakis, CA. Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit (PRKAR1A) in patients with the “complex of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas” (Carney complex). Ann N Y Acad Sci 2002; 968: 3–21.CrossRefGoogle ScholarPubMed