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Diagnosis of Carney complex following multiple recurrent cardiac myxomas.

Authors :
Yokoyama S
Nagao K
Higashida A
Aoki M
Yamashita S
Fukuda N
Doi T
Yamashita A
Fukahara K
Yoshimura N
Source :
General thoracic and cardiovascular surgery [Gen Thorac Cardiovasc Surg] 2022 Jan; Vol. 70 (1), pp. 87-91. Date of Electronic Publication: 2021 Oct 12.
Publication Year :
2022

Abstract

Carney complex is a rare syndrome caused by a genetic mutation leading to multiple endocrine abnormalities and a variety of tumors. Here, we report a case of Carney complex diagnosed due to recurrent multiple myxomas in the right atrium of a patient 16 years after the resection of the primary left atrial myxoma. Surgical excision was performed for the multiple recurrent right atrial tumors under cardiopulmonary bypass. The patient remained complication-free after surgery and was discharged on the 14th day. He was scheduled to continue echocardiographic follow-up and periodic systemic review by an endocrinologist. This case emphasizes the fact that if cardiac myxomas tend to be multiple and recurrent at a relatively young age, the possibility of Carney complex should be considered, even in the absence of any other related feature other than cardiac tumors.<br /> (© 2021. The Author(s).)

Details

Language :
English
ISSN :
1863-6713
Volume :
70
Issue :
1
Database :
MEDLINE
Journal :
General thoracic and cardiovascular surgery
Publication Type :
Academic Journal
Accession number :
34642893
Full Text :
https://doi.org/10.1007/s11748-021-01719-w