Treatment of Nevirapine-Associated DRESS Syndrome with Intravenous Immune Globulin (IVIG)
July 2005 | Volume 4 | Issue 4 | Case Reports | 510 | Copyright © July 2005
Katherine S. Fields MD, Marta J. Petersen MD, Elizabeth Chiao MD MPH, Payam Tristani-Firouzi MD
Abstract
Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome is an adverse drug reaction most commonly
associated with aromatic antiepileptic agents. It is characterized by the triad of skin eruption, fever, and systemic
involvement, with the latter usually manifesting as hepatitis and lymphadenopathy.1 Mortality is primarily due to
hepatic failure and can be as high as 10%.2 Formerly referred to by names such as Dilantin hypersensitivity syndrome
and anticonvulsant hypersensitivity syndrome, DRESS syndrome is a more precise term since this reaction pattern can
be seen with other agents. DRESS syndrome has also been reported in association with sulfonamides, allopurinol,
terbinafine, minocycline, azathioprine, and dapsone3 as well as with several antiretroviral agents such as abacavir and
nevirapine.4,5 We describe a patient with HIV who developed nevirapine hypersensitivity syndrome who was successfully treated with intravenous immune globulin (IVIG).