Syndrome in question. MAGIC syndrome.

The authors present a male 40-year-old patient with established diagnosis of Behçet's disease which had evolved to recurrent bilateral auricular polychondritis crises. MAGIC syndrome (mouth and genital ulcers with inflamed cartilage) is rare and groups together patients with this clinical picture without necessarily fulfilling the clinical criteria for Behçet's disease or relapsing polychondritis, demonstrating an independent disorder.

Treatment of acral persistent papular mucinosis with electrocoagulation.

Background: Acral persistent papular mucinosis is a rare localized form of lichen myxedematosus with few case reports and no documented therapeutic options.

Objective: To report full resolution of acral persistent papular mucinosis after electrocoagulation.

Methods: Case report of a 51-year-old white female diagnosed with an acral persistent papular mucinosis.