A rare clinic type of angiokeratoma: angiokeratoma circumscriptum naeviforme

Abstract

Angiokeratomas are verrucous, hyperkeratotic, red-black, well-demarcated papules and plaques consisting of vascular enlargement and hyperkeratosis [1]. Five different clinical variants of angiokeratoma have been identifined including angiokeratoma corporis diffusum (Fabry's disease), angiokeratoma Mibelli, angiokeratoma Fordyce, angiokeratoma circumscriptum, solitary and multiple angiokeratomas [2]. Angiokeratoma circumscriptum naeviforme, is a rare clinic type of angiokeratomas [1]. We report here a case of angiokeratoma circumscriptum naeviforme, on the lower extremity of a male patient.