Abstract
Background: Lymphomatoid papulosis (LyP) is an indolent CD30 positive lymphoproliferative disorder characterized by recurrent, self-healing papulo-nodules. LyP type E is a recently described rare subtype of lymphomatoid papulosis. It is distinguished by its angiocentric and angiodestructive histologic features and larger, eschar-like ulcerations. The diagnosis of LyP type E depends on clinical, histologic, and immunohistochemical findings rather than TCR clonality studies.
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