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Left ventricular non-compaction in a patient with Shone's complex

Mehrnoush Toufan1, Lelll Pourafkari1, Aldln Baghbani-Oskouel2

  • 1Department of Cardiology, Cardiovascular Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Turk Kardiyoloji Dernegi Arsivi : Turk Kardiyoloji Derneginin Yayin Organidir
|September 5, 2019
PubMed

Insights

Shone's complex, a rare congenital heart defect with multiple left-sided obstructions, was unusually found in an adult with left ventricular non-compaction cardiomyopathy (NCC). This previously undescribed association highlights a new diagnostic consideration for complex cardiac conditions.

Area of Science:

  • Cardiology
  • Congenital Heart Disease
  • Cardiomyopathy

Background:

  • Shone's complex involves multiple obstructive lesions in the left heart.
  • Congenital cardiac malformations require ongoing research for diagnosis and treatment.

Observation:

  • An adult male presented with palpitations and dyspnea.
  • Echocardiography identified Shone's complex.

Findings:

  • The patient was diagnosed with Shone's complex.
  • Left ventricular non-compaction cardiomyopathy (NCC) was also identified.
  • This co-occurrence of Shone's complex and NCC is novel.

Implications:

  • This case expands the understanding of Shone's complex presentations.
  • It suggests NCC should be considered in adults with Shone's complex.
  • Further research is needed to explore this association and its clinical significance.

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