Journal
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
Volume 68, Issue 5, Pages 721-728Publisher
MOSBY-ELSEVIER
DOI: 10.1016/j.jaad.2012.10.017
Keywords
complication; corticosteroid; drug-induced hypersensitivity syndrome; drug reaction; drug reaction with eosinophilia and systemic symptoms; herpesvirus; outcome; treatment; viral reactivation
Categories
Funding
- Research on Measures for Intractable Diseases Project
- Ministry of Health, Labor, and Welfare
- Ministry of Education, Culture, Sports, Science, and Technology
- Grants-in-Aid for Scientific Research [22591250] Funding Source: KAKEN
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Background: Drug-induced hypersensitivity syndrome (DIHS)/drug reaction with eosinophilia and systemic symptoms (DRESS) is a severe systemic hypersensitivity reaction caused by specific drugs, in which herpesvirus reactivations and organ dysfunction occur during the course of the disease. Although recent reports have documented the development of autoimmune disease after complete resolution of DIHS/DRESS, relatively little is known about long-term outcomes after complete resolution of the disease. Objective: The aim of this study was to retrospectively analyze complications and sequelae in the early and late phases of DIHS/DRESS according to treatment. Methods: In all, 34 patients were classified into 2 groups: 14 patients with oral corticosteroid treatment; and 20 with noncorticosteroid treatment. The disease time course was divided into 2 periods: the first 6 months after onset of the drug reaction (early phase); and the period thereafter (late phase). Investigations to detect the presence of viral/bacterial infectious diseases, organ dysfunction, and autoantibodies were performed in both early and late phases. Results: Herpesvirus infections and pneumonia were detected in 6 and 2 patients, respectively, in the corticosteroid treatment group in the early phase. In the noncorticosteroid treatment group, 2 patients developed autoimmune diseases, namely lupus erythematosus and autoimmune thyroiditis. Autoantibodies were detected in 44.4% of patients examined in the late phase of the disease. Limitations: This study only evaluated a small number of autoantibodies. Conclusion: The need for anti-inflammatory effects from systemic corticosteroids should be balanced with the risk of infectious diseases and the benefits of preventing the appearance of later autoimmune conditions in patients with DIHS/DRESS. (J Am Acad Dermatol 2013;68:721-8.)
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