A 65-year-old woman presented with dyspnea and bilateral leg edema for 1 week, worsening fatigue for 1 month, and a 7-lb weight loss over the last summer. She was clinically and biochemically hyperthyroid. Echocardiography revealed a left atrial myxoma measuring 6.2 × 3.3 cm protruding into the mitral orifice and left ventricle during diastole. She was treated for Gravesʼ disease with Iodine-131. Six weeks later, her left atrial myxoma measuring 10.1 × 6.2 × 2.4 cm was resected. She became euthyroid before surgery and then biochemically hypothyroid 6 weeks after radioiodine treatment, for which she subsequently required thyroxine replacement. Atrial myxomas are the most common primary cardiac neoplasms. At least 5% to 10% can be attributed to Carneyʼs complex. More than two-thirds of patients with Carneyʼs complex develop one or more cardiac myxomas. Although atrial myxomas in Carneyʼs complex are histologically indistinguishable from the sporadic form, their clinical presentation and course is distinct. This is the first case of newly diagnosed Gravesʼ disease that has been reported in association with an atrial myxoma. The features discussed in this article help differentiate between syndromic and sporadic atrial myxomas.