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Recurrent Cardiac Myxoma: Insights From a Fourth Recurrence
Manuela Cristina Ribeiro Dias Barroso1, Heleutério da Conceição Nicolau Madogolele1, Hernán Patrício García Mejía1
1Instituto do Coração (InCor), Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Insights
Recurrent cardiac myxomas, rare in benign tumors, occurred in a patient with Carney complex (CNC). This case highlights the need for advanced imaging and genetic testing for managing this rare syndrome.
Area of Science:
- Cardiology
- Genetics
- Oncology
Background:
- Cardiac myxomas are the most common benign cardiac tumors.
- Recurrences are rare, typically associated with Carney complex (CNC).
Observation:
- A 49-year-old woman with CNC experienced recurrent cardiac myxomas requiring four surgeries over 14 years.
- She developed an ischemic stroke, necessitating further interventions.
Findings:
- Carney complex is a rare autosomal dominant syndrome.
- Recurrent cardiac myxomas in CNC can affect multiple heart chambers.
Implications:
- This case emphasizes the critical role of advanced imaging techniques like echocardiography and MRI.
- Early diagnosis and genetic evaluation are crucial for effective management of CNC and its cardiac manifestations.
Background:
Cardiac myxomas are the most common benign cardiac tumors, and recurrences are rare except in Carney complex (CNC).
Case Summary:
A 49-year-old woman with CNC and recurrent cardiac myxomas underwent 4 surgeries over 14 years. Initially asymptomatic, she later developed ischemic stroke. Echocardiography and magnetic resonance imaging confirmed the diagnosis, necessitating repeated surgical resections and ongoing surveillance.
Discussion:
CNC is a rare autosomal dominant syndrome causing recurrent cardiac myxomas that can affect multiple cardiac chambers. This case underscores the importance of advanced imaging and genetic evaluation for early diagnosis and management.
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