Pereira da Silva Tânia, Santos Maria Luis, Brito Ana Patrícia, Fernandes Magda, Cotter Jorge
Internal Medicine, Unidade Local de Saúde do Alto Ave, Guimarães, PRT.
Cureus. 2025 Aug 4;17(8):e89368. doi: 10.7759/cureus.89368. eCollection 2025 Aug.
Toxic epidermal necrolysis (TEN) is a rare, life-threatening mucocutaneous condition, most commonly triggered by drugs, with particularly high mortality in elderly populations. The medications most frequently associated with TEN include antibiotics such as sulfamethoxazole-trimethoprim (sulfonamides), penicillins, cephalosporins, and quinolones (e.g., ciprofloxacin); anticonvulsants such as phenytoin, carbamazepine, and lamotrigine; nonsteroidal anti-inflammatory drugs (NSAIDs), especially oxicam derivatives (e.g., piroxicam), and, less commonly, ibuprofen; allopurinol; nevirapine; and other agents such as paracetamol, celecoxib, tyrosine kinase inhibitors, and immunobiological therapies like infliximab. We describe a 71-year-old, functionally dependent male who developed fever and progressive skin detachment after self-medicating with paracetamol and ibuprofen. Examination revealed widespread bullae and skin sloughing involving approximately 70% of his total body surface area (TBSA). Despite supportive measures, the patient rapidly deteriorated and died on the second day of hospitalization. TEN was assumed as the primary cause of death. The prognosis in TEN is strongly influenced by age, comorbidities, and the extent of skin involvement. Genetic predispositions, such as HLA-B (associated with carbamazepine-induced TEN, particularly in Southeast Asian populations), HLA-A31:01 (carbamazepine hypersensitivity in European, Japanese, and Latin American populations), and HLA-B*58:01 (allopurinol-induced TEN in Asian populations), are important risk factors that guide genetic screening recommendations before prescribing certain high-risk drugs. Supportive care remains the mainstay of treatment for TEN, focusing on meticulous wound care, fluid and electrolyte management, infection prevention, and pain control. However, the use of immunomodulatory therapies, such as corticosteroids, cyclosporine, and biologics, remains a subject of ongoing debate, with inconsistent evidence regarding their efficacy. Timely recognition of TEN and immediate cessation of the offending drug are paramount to improving patient outcomes and reducing mortality. This case highlights the potential role of ibuprofen, a commonly used over-the-counter NSAID, as a trigger for TEN, particularly in frail elderly individuals. Although ibuprofen is generally considered a low-risk medication, its capacity to induce severe cutaneous adverse reactions should not be underestimated. The prognosis in TEN is heavily influenced by factors such as advanced age, existing comorbidities, and the extent of skin involvement. Given the high fatality rates associated with TEN, especially in older adults, clinicians should maintain a high index of suspicion in patients presenting with acute mucocutaneous symptoms following recent drug exposure, including over-the-counter medications like ibuprofen, and emphasize the importance of public education on the dangers of unsupervised self-medication.
中毒性表皮坏死松解症(TEN)是一种罕见的、危及生命的皮肤黏膜疾病,最常见的诱因是药物,在老年人群中死亡率尤其高。与TEN最常相关的药物包括抗生素,如磺胺甲恶唑-甲氧苄啶(磺胺类药物)、青霉素、头孢菌素和喹诺酮类(如环丙沙星);抗惊厥药,如苯妥英、卡马西平和拉莫三嗪;非甾体抗炎药(NSAIDs),尤其是奥昔康衍生物(如吡罗昔康),较少见的有布洛芬;别嘌醇;奈韦拉平;以及其他药物,如对乙酰氨基酚、塞来昔布、酪氨酸激酶抑制剂和免疫生物疗法如英夫利昔单抗。我们描述了一名71岁、功能依赖的男性,他在自行服用对乙酰氨基酚和布洛芬后出现发热和进行性皮肤脱落。检查发现广泛的水疱和皮肤剥脱,累及全身表面积(TBSA)约70%。尽管采取了支持措施,患者病情迅速恶化,在住院第二天死亡。TEN被认为是主要死因。TEN的预后受年龄、合并症和皮肤受累程度的强烈影响。遗传易感性,如HLA-B(与卡马西平诱导的TEN相关,特别是在东南亚人群中)、HLA-A31:01(在欧洲、日本和拉丁美洲人群中的卡马西平超敏反应)和HLA-B*58:01(在亚洲人群中的别嘌醇诱导的TEN),是重要的风险因素,可指导在开具某些高风险药物之前进行基因筛查建议。支持性护理仍然是TEN治疗的主要支柱,重点是精心的伤口护理、液体和电解质管理、感染预防和疼痛控制。然而,免疫调节疗法的使用,如皮质类固醇、环孢素和生物制剂,仍然是一个持续争论的话题,关于其疗效的证据并不一致。及时识别TEN并立即停用致病药物对于改善患者预后和降低死亡率至关重要。本病例突出了常用的非处方NSAID布洛芬作为TEN诱因的潜在作用,特别是在体弱的老年人中。尽管布洛芬通常被认为是一种低风险药物,但其诱发严重皮肤不良反应的能力不应被低估。TEN的预后受到高龄、现有合并症和皮肤受累程度等因素的严重影响。鉴于TEN相关的高死亡率,特别是在老年人中,临床医生对于近期药物暴露后出现急性皮肤黏膜症状的患者,包括像布洛芬这样的非处方药物,应保持高度怀疑,并强调公众教育关于无监督自行用药危险的重要性。