Abstract
Carney Complex is a multiple endocrine neoplasia syndrome caused by a mutation in PRKAR1A gene. Tumor sites include skin (lentigines, blue nevus, cutaneous myxomas, palpebral lentigines), pituitary (somatotroph hyperplasia/adenomas), adrenal (primary pigmented nodular adrenal hyperplasia (PPNAD)), cardiac (myxomas), and testes (large cell calcifying sertoli cell tumor).We will present a family with a variety of distinct conditions related to Carney Complex, who were effectively treated to prevent secondary endocrine complications.
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