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A case of multiple eccrine angiomatous hamartoma ��EAH�� is reported. EAH is a rare condition histologically characterized by increased eccrine structures and numerous vascular elements. An eight-year-old girl was admitted to the hospital for 4-year history painful subcutaneous nodules and 1-year history local hyperhidrosis and hypertrichosis. The diagnosis of EAH was made by clinical manifestation and histological examination. Superficial X-ray radiotherapy showed no significant efficacy, and the lesions were finally removed by several sessions of surgical therapy. These results demonstrate that surgical therapy is appropriate for EAH.