Diagnosis of Carney complex following multiple recurrent cardiac myxomas.
Diagnosis of Carney complex following multiple recurrent cardiac myxomas.
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DOI:
10.1007/s11748-021-01719-w
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发表时间:
2022-01
影响因子:
1.2
通讯作者:
Yoshimura N
中科院分区:
文献类型:
--
作者:
Yokoyama S;Nagao K;Higashida A;Aoki M;Yamashita S;Fukuda N;Doi T;Yamashita A;Fukahara K;Yoshimura N
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.
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影响因子:
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