Abstract
Necrolytic migratory erythema (NME) is a rare cutaneous finding characterized by painful, pruritic, scaly red patches and plaques, bullae, and superficial erosions. Typically NME is a paraneoplastic phenomenon associated with glucagonoma. We report the exceptional case of an infant who developed iatrogenic NME arising secondary to glucagon therapy for congenital hyperinsulinism.
Original language | English |
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Pages (from-to) | e43-e47 |
Journal | Pediatric Dermatology |
Volume | 33 |
Issue number | 2 |
DOIs | |
State | Published - Mar 1 2016 |