Abstract
Syringocystadenoma papilliferum (SCAP) is a benign adnexal neoplasm with apocrine differentiation.1,2 which may be derived from pluripotent cells.3 The lesion may develop within a pre-existing nevus sebaceus, but the majority of cases arise sporadically.3 Congenital lesions in a Blaschkoid distribution have also been reported, and these cases are thought to represent genetic mosaicism.4,5,6 The tumor has a varied clinical appearance, but typically presents as a raised warty, hairless plaque or nodule.3
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