多发性小汗腺血管瘤样错构瘤一例

Multiple eecrine angiomatous hamartoma：a ease report

报道1例多发性小汗腺血管瘤样错构瘤。小汗腺血管瘤样错构瘤是一种少见的皮肤肿瘤，病理表现为增多的小汗腺结构和大量血管成分。本例患儿8岁，左前臂多发性皮下结节伴疼痛4年，近1年局部出现多汗、多毛。经组织病理检查结合临床表现，诊断为小汗腺血管瘤样错构瘤。浅层X线照射后效果不明显，后进行分次手术切除，疗效较佳。提示治疗小汗腺血管错构瘤选择适当的手术方案是可行的。

A case of multipl.e 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.