A 21-year-old female with a history of cutaneous myxoma presented with multicentric cardiac myxomas and endocrinopathy, leading to a diagnosis of Carney complex syndrome.
Case Report (n=1)
This case highlights a rare presentation of Carney complex characterized by multicentric cardiac myxomas involving all four chambers alongside multiple endocrinopathies.
Carney complex is a rare autosomal dominant disorder characterized by multiple tumors, including cardiac and extracardiac myxomas, skin lesions, and various endocrine disorders. We are reporting a 21-year-old female patient with past surgical history significant for excision of a cutaneous myxoma who presented with multicentric cardiac myxomas involving the four cardiac chambers. She also presented with endocrinal disorders in the form of an enlarged right lobe of the thyroid, hyperthyroid state, and an incidentally noted adrenal cyst; hence, she was diagnosed with carney complex syndrome.
Saleh et al. (Mon,) conducted a case report in Carney complex (n=1). A 21-year-old female with a history of cutaneous myxoma presented with multicentric cardiac myxomas and endocrinopathy, leading to a diagnosis of Carney complex syndrome.
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