4.0 Article

Refractory angiolymphoid hyperplasia with eosinophilia: Complete resolution with low dose thalidomide

Journal

PEDIATRIC DERMATOLOGY
Volume 39, Issue 6, Pages 995-996

Publisher

WILEY
DOI: 10.1111/pde.15061

Keywords

angiolymphoid hyperplasia with eosinophilia; refractory; symptomatic; thalidomide; treatment

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ALHE is a rare benign vascular proliferative condition that usually occurs in the head and neck area, particularly near the ear, presenting as painless vascular papules or nodules. We report a case of ALHE that failed multiple therapeutic interventions but achieved complete resolution when treated with thalidomide.
Angiolymphoid hyperplasia with eosinophilia (ALHE) is a difficult-to-treat and rare benign vascular proliferative condition which presents as painless, solitary, or multiple vascular papules or nodules in the head and neck area, with predilection for the ear. We report a case of ALHE that failed multiple therapeutic interventions but achieved complete resolution when treated with thalidomide.

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