Diagnosis of Carney complex following multiple recurrent cardiac myxomas

Shigeki Yokoyama*, Kanetsugu Nagao, Akihiko Higashida, Masaya Aoki, Shigeyuki Yamashita, Nobuyuki Fukuda, Toshio Doi, Akio Yamashita, Kazuaki Fukahara, Naoki Yoshimura

*この論文の責任著者

研究成果: ジャーナルへの寄稿学術論文査読

6 被引用数 (Scopus)

抄録

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.

本文言語英語
ページ(範囲)87-91
ページ数5
ジャーナルGeneral Thoracic and Cardiovascular Surgery
70
1
DOI
出版ステータス出版済み - 2022/01

ASJC Scopus 主題領域

  • 外科
  • 呼吸器内科
  • 循環器および心血管医学

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