Khurana Vinod K, Mehta Raj K, Chaudhary Deepak, Pant Leela
Department of Dermatology and Venereology, Hindu Rao Hospital, Delhi, India.
Indian J Dermatol. 2013 Sep;58(5):405. doi: 10.4103/0019-5154.117306.
An 18 years old male presented with a slowly increasing multiple papulonodular lesions on his left leg since birth. No definite diagnosis was made on clinical ground. But verrucous epidermal naevus with secondary change and appendageal tumor was suspected on clinical examination. Histopathological examination revealed syringocystadenoma papilliferm (SCAP). SCAP is very rare on lower leg. Only one case of SCAP on lower leg has been reported in literature so far, which was superimposed on an organoid nevus. The case is reported for unusual location and unusual presentation.
一名18岁男性自出生以来左腿出现逐渐增多的多发性丘疹结节性损害。临床检查未明确诊断。但临床检查怀疑为伴有继发改变的疣状表皮痣和附属器肿瘤。组织病理学检查显示为乳头状汗管囊腺瘤（SCAP）。SCAP在小腿非常罕见。迄今为止，文献中仅报道过1例小腿的SCAP，其叠加于器官样痣之上。现报道此病例因其不寻常的部位和表现。
