Treatment of DIHS/DRESS syndrome with combined N-acetylcysteine, prednisone and valganciclovir - a hypothesis

被引:48
作者
Moling, Oswald [1 ]
Tappeiner, Lukas [2 ]
Piccin, Andrea [3 ]
Pagani, Elisabetta [4 ]
Rossi, Patrizia [4 ]
Rimenti, Giovanni [1 ]
Vedovelli, Claudio [1 ]
Mian, Peter [1 ]
机构
[1] Osped Gen, Div Infect Dis, I-39100 Bolzano, Italy
[2] Osped Gen, Div Dermatol, I-39100 Bolzano, Italy
[3] Osped Gen, Div Haematol, I-39100 Bolzano, Italy
[4] Osped Gen, Lab Microbiol & Virol, I-39100 Bolzano, Italy
来源
MEDICAL SCIENCE MONITOR | 2012年 / 18卷 / 07期
关键词
drug-induced hypersensitivity syndrome; drug reaction with eosinophilla and systemic symptoms; HHV-6; N-acetylcysteine; valganciclovir; INDUCED HYPERSENSITIVITY SYNDROME; ACUTE LIVER-FAILURE; HUMAN-HERPESVIRUS; 6; REGULATORY T-CELLS; SEVERE DRUG ERUPTIONS; SYSTEMIC SYMPTOMS; HUMAN-HERPESVIRUS-6; REACTIVATION; ACETAMINOPHEN; METABOLITES; EOSINOPHILIA;
D O I
10.12659/MSM.883198
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Drug-induced hypersensitivity syndrome/drug reaction with eosinophilia and systemic symptoms (DIHS/DRESS) is a rare and severe adverse drug reaction with an associated mortality of 10-20%. Clinical worsening despite discontinuation of the culprit drug is considered a characteristic feature of DIHS/DRESS. Besides the early recognition of the syndrome and discontinuation of its causative drug, the mainstay of treatment is systemic corticosteroids. Nevertheless, treatment of severe DIHS/DRESS is not well defined, as corticosteroids may sometimes not be effective, and decreasing the dose may be associated with flaring of the disease. Case Report: A 38-year-old woman with high fever, malaise, abdominal pain, rash, and elevated liver enzymes received immediate high-dose N-acetylcysteine, because acetaminophen hepatotoxicity was suspected. N-acetylcysteine administration was associated with a significant clinical improvement. However, within the next week DIHS/DRESS syndrome was diagnosed, which explained all the symptoms, and which was subsequently treated with prednisone and valganciclovir. Conclusions: New options necessary to improve treatment of severe DIHD/DRESS have to consider its sequential pathogenetic mechanisms. N-acetylcysteine might neutralize the drug-derived reactive metabolites, which are responsible for protein adduct formation and specific T cell stimulation, and replete the glutathione stores that counterbalance oxidative stress. Prednisone might inhibit lymphoproliferation and valganciclovir might prevent complications related to HHV-6 reactivation. We therefore propose the unprecedented combination of N-acetylcysteine, prednisone and valganciclovir as a treatment option for DIHS/DRESS.
引用
收藏
页码:CS57 / CS62
页数:6
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