Stevens–Johnson syndrome with visceral arteritis due to sulphonylurea therapy

Authors

C Duncan, AJ Sommerfield, I Nawroz, IW Campbell

Abstract

A 67‐year‐old male with recently diagnosed type 2 diabetes mellitus presented with clinical features characteristic of Stevens–Johnson syndrome and died from a haemorrhagic bronchopneumonia. Autopsy revealed features of granulomatous arteritis and an interface cholestatic hepatitis. The cause of these features was felt to be due to a hypersensitivity reaction to glibenclamide. Although unusual, drug hypersensitivity with sulphonylureas may be fatal. Copyright © 2004 John Wiley & Sons, Ltd.

Digital Object Identifier (DOI)

10.1002/pdi.644 About DOI

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