Key result
A 13-year-old boy presented with xanthoma tuberosum, a typical history of angina pectoris, and significant electrocardiographic changes.
Case Report (n=1)
No
Highlights a rare case of severe premature coronary artery disease and angina pectoris in a child with xanthoma tuberosum.
Alerts clinicians to angina in children with xanthoma tuberosum; leaves open systematic screening for premature CAD in familial hypercholesterolemia.
DISEASE of the coronary arteries alone or with angina pectoris is rarely found in children. For that reason it is thought of interest and importance to report the case of a boy 13 years of age who had xanthoma tuberosum, a typical history of angina pectoris and significant changes in the electrocardiogram, and to review similar cases from the literature. REPORT OF A CASE The patient, a boy 13 years old, was first seen at the Mayo Clinic on Aug. 22, 1945. Seven years previously soft, fluctuant, yellowish pink, circumscribed tumors had begun to develop on the elbows, knees, ankles, joints of the fingers and toes and the buttocks. On two occasions similar lesions had been removed surgically from the heel and knee, and they had been reported to contain white material like cottage cheese. The masses had never been tender. For six to eight months before admission the patient
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Charles D. Cook (1947) conducted a case report in Xanthoma tuberosum and angina pectoris (n=1). A 13-year-old boy presented with xanthoma tuberosum, a typical history of angina pectoris, and significant electrocardiographic changes.
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