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

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

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.

Original languageEnglish
Pages (from-to)87-91
Number of pages5
JournalGeneral Thoracic and Cardiovascular Surgery
Volume70
Issue number1
DOIs
StatePublished - 2022/01

Keywords

  • Carney complex
  • Cryoablation for myxoma
  • Recurrent of cardiac myxoma

ASJC Scopus subject areas

  • Surgery
  • Pulmonary and Respiratory Medicine
  • Cardiology and Cardiovascular Medicine

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