Fariña M C, Soriano M L, Escalonilla P, Piqué E, Martín L, Barat A, Requena L
Department of Dermatology, Fundación Jiménez Díaz, Universidad Autónoma, Madrid, Spain.
Am J Dermatopathol. 1996 Aug;18(4):417-9. doi: 10.1097/00000372-199608000-00016.
We report a case of areolar sebaceous hyperplasia involving the right mammary areola in a 49-year-old male. Areolar sebaceous hyperplasia, an uncommon entity first described by Catalano and Ioannides in 1985, is characterized clinically by yellowish thickening of the areolae and histopathologically by large numbers of mature hyperplastic sebaceous lobules connected to the skin surface through short, hairless infundibular canals. Since its original description, only two additional reports have been published. To our knowledge, our patient is the first reported of areolar sebaceous hyperplasia in a male.
我们报告一例49岁男性右侧乳晕皮脂腺增生病例。乳晕皮脂腺增生是一种罕见病症，于1985年由卡塔拉诺和约阿尼季斯首次描述，其临床特征为乳晕发黄增厚，组织病理学特征为大量成熟的增生性皮脂腺小叶通过短而无毛的漏斗状导管与皮肤表面相连。自最初描述以来，仅另外发表了两篇报告。据我们所知，我们的患者是首例报告的男性乳晕皮脂腺增生病例。
