Rabens S F, Naness J I, Gottlieb B F
Arch Dermatol. 1976 Apr;112(4):520-2.
A patient had two fleshy, nontender masses, each partially filling an axillary vault. These tumors arose at puberty in normal-appearing axillae. The masses were accompanied by localized hyperhidrosis. Histopathological examination of the lesions showed that the reticular layer of the dermis had been replaced solely by lobular masses of unencapsulated, mature apocrine elements. These very rare tumors are best classified as apocrine gland organic hamartomas, or apocrine nevi. To our knowledge, such a case has never been reported or photographed.
一名患者有两个肉质、无压痛的肿块，每个肿块部分填充腋窝。这些肿瘤在青春期出现在外观正常的腋窝。肿块伴有局部多汗症。病变的组织病理学检查显示，真皮网状层仅被小叶状、无包膜、成熟的顶泌汗腺成分所取代。这些非常罕见的肿瘤最好归类为顶泌汗腺器官样错构瘤或顶泌汗腺痣。据我们所知，从未有过此类病例的报道或照片。
