Elastosis perforans serpiginosa related to vascular Ehlers-Danlos syndrome
Published Web Locationhttps://doi.org/10.5070/D3253043337
Elastosis perforans serpiginosa (EPS) is a rare skin disease with elimination of connective tissue fibers from dermis to epidermis. The typical presentation shows hyperkeratotic red or skin-colored papules arranged in a circinate pattern. We present a 26-year-old woman with EPS known to have vascular Ehlers-Danlos syndrome.