[Incidental diagnosis of cor triatriatum sinister in a young woman]

Rita Cristina Myriam Intravaia1, Michele Massimo Gulizia1

  • 1U.O.C. Cardiologia con UTIC, Azienda di Rilievo Nazionale e Alta Specializzazione "Garibaldi", P.O. "Garibaldi-Nesima", Catania.

Giornale Italiano Di Cardiologia (2006)
|May 27, 2026
PubMed

Insights

Cor triatriatum sinister (CTS) is a rare congenital heart defect where a membrane divides the left atrium. Echocardiography is key for diagnosing CTS in adults and guiding management, even in asymptomatic cases.

Area of Science:

  • Cardiology
  • Congenital Heart Disease
  • Cardiac Imaging

Background:

  • Cor triatriatum sinister (CTS) is a rare congenital heart defect, affecting 0.1-0.4% of cases.
  • It is characterized by a fibromuscular septum dividing the left atrium into two chambers.
  • Diagnosis in adulthood is uncommon, often incidental.

Purpose of the Study:

  • To report a case of incidentally diagnosed Cor triatriatum sinister in a 37-year-old woman.
  • To highlight the role of echocardiography in diagnosis and risk stratification.
  • To discuss the management of asymptomatic CTS in adults.

Main Methods:

  • Transthoracic echocardiography (TTE) for initial assessment.
  • Transesophageal echocardiography (TEE) for detailed characterization.
  • Classification using the Loeffler criteria.

Main Results:

  • Incidental diagnosis of CTS in a 37-year-old woman presenting with chest pain.
  • TTE revealed a left intra-atrial membrane; TEE confirmed no significant hemodynamic impact.
  • Patient classified as Loeffler group III due to membrane patency and non-significant gradient.
  • No significant associated cardiac anomalies were identified.

Conclusions:

  • Echocardiography is crucial for diagnosing and assessing the hemodynamic significance of CTS in adults.
  • Asymptomatic patients with non-obstructive CTS generally have a favorable prognosis.
  • Long-term arrhythmia monitoring is recommended due to risks of atrial fibrillation and cardioembolic events.

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