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An Undiagnosed Shone Complex in a 52-Year-Old Female: A Case Report
Lila H Abu-Hilal1, Yumna Njoum1, Duha I Barghouthi1
1Al-Quds University, Jerusalem, Palestine.
This case report details a rare late diagnosis of Shone complex (SC), a congenital heart defect, in a 52-year-old woman. It highlights the importance of considering incomplete SC in adults with left-sided obstructive heart lesions.
Area of Science:
- Cardiology
- Congenital Heart Disease
- Adult Congenital Heart Disease
Background:
- Shone complex (SC) is a rare congenital heart disease characterized by multiple left-sided obstructive anomalies.
- SC typically presents in early childhood, making adult diagnoses uncommon.
Observation:
- A 52-year-old female with a history of hypertension presented with dyspnea and palpitations.
- Investigations revealed severe aortic and mitral stenosis, and aortic coarctation, suggesting an incomplete SC.
Findings:
- The patient was diagnosed with an incomplete Shone complex at 52 years old, a rare late presentation.
- Diagnostic imaging confirmed bicuspid aortic valve with severe stenosis, parachute mitral valve with severe stenosis, and aortic coarctation with collateral circulation.
Implications:
- This case underscores the possibility of late presentations of SC, even in adulthood.
- Highlights the need for early diagnosis and intervention for SC to improve patient outcomes.
- Emphasizes considering incomplete SC in adult patients with complex left-sided obstructive cardiac lesions.
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