Valdecoxib-associated acute generalized exanthematous pustulosis

被引:33
作者
Byerly, FL
Nelson, KC
Granko, RP
Morrell, DS
Cairns, BA
机构
[1] Univ N Carolina Hosp, N Carolina Jaycee Burn Ctr CB 7600, Dept Surg, Chapel Hill, NC 27514 USA
[2] Univ N Carolina, Dept Dermatol, Chapel Hill, NC 27514 USA
[3] Univ N Carolina Hosp, Dept Pharm, UNC Ctr Medicat Safety & Adverse Drug React Repor, Chapel Hill, NC 27514 USA
[4] Univ N Carolina, Div Trauma Crit Care & Burns, Chapel Hill, NC 27599 USA
关键词
valdecoxib-associated; acute generalized exanthematous pustulosis; toxic epidermal necrolysis;
D O I
10.1016/j.burns.2004.10.017
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
AGEP (acute generalized exanthematous pustulosis) is a relatively rare exfoliative skin syndrome consisting of generalized eruption of pustules in response to medication or infection. Because AGEP may have other systemic manifestations, such as renal failure, hyperthermia, lab abnormalities, and/or hemodynamic instability, it is important to make the distinction between AGEP and other life-threatening generalized skin diseases, such as toxic epidermal necrolysis (TEN). Here we present a case of AGEP in response to valdecoxib, which has not previously been described in the literature. The patient presented with profound hypotension requiring fluid and vasopressor support and was referred to the burn service for treatment of TEN, but her skin lesions were inconsistent with this diagnosis. A dermatology consult was obtained and suggested a diagnosis of AGEP, which a biopsy confirmed. TEN and AGEP present with similar history, types of associated drugs, and immunology. Both can be associated with antibiotics, nonsteroidals, and anticonvulsants, but AGEP is more frequent with aminopenicillins, while TEN is associated more often with sulfonamide antibiotics. Both disorders have a proposed T cell-mediated immune response, but they differ in the mechanism. A description of valdecoxib and its role as a sulfonamide in producing cutaneous reactions is also provided. (c) 2004 Elsevier Ltd and ISBI. All rights reserved.
引用
收藏
页码:383 / 387
页数:5
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