Abstract
Acquired ichthyosis (AI) is a group of cornification disorders characterized clinically by dry, rough skin with prominent desquamation, mostly in adulthood. It may be associated with a wide variety of systemic diseases (autoimmune/inflammatory, metabolic, endocrine, infectious), drug reactions or as a paraneoplastic manifestation of several hematologic or solid neoplasms [1]. We report two patients who developed AI in the context of a primary cutaneous CD30+ lymphoproliferative disorder (CD30+ LPD): [...]
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