Departments of Dermatology, Hospital Universitario 12 de Octubre, I + 12 Research Institute, Universidad Complutense, Madrid, Spain.
Departments of Pathology, Hospital Universitario 12 de Octubre, I + 12 Research Institute, Universidad Complutense, Madrid, Spain.
Br J Dermatol. 2018 Mar;178(3):786-789. doi: 10.1111/bjd.15400. Epub 2017 Oct 1.
A 65-year-old pluripathological woman attended our hospital with a cutaneous eruption of sudden appearance after vancomycin treatment. She presented targetoid lesions affecting approximately 25-30% of her body surface, large erosions with mucosal lesions and positive Nikolsky sign. Under the initial clinical suspicion of toxic epidermal necrolysis (TEN), and considering the recent literature of successful use of etanercept in these cases, she was treated with a single dose of this antitumour necrosis factor (anti-TNF) agent. Subsequently, the exanthema progression stopped and resolution of the lesions happened in a few days. Later on, histopathology revealed a subepidermal blister with dense neutrophilic infiltrate and linear deposits of immunoglobulin A (IgA) on the dermoepidermal junction, allowing us to establish the diagnosis of drug-induced linear IgA dermatosis mimicking TEN. Linear IgA dermatosis can have severe clinical manifestations, even mimicking TEN, and can have high mortality, especially in drug-induced cases. We have not found any other report of linear IgA dermatosis treated with etanercept in the English literature. Anti-TNF medications could represent useful therapeutic alternatives in this dermatosis.
一位 65 岁的多系统疾病女性患者在万古霉素治疗后突发皮肤疹,来我院就诊。她表现为靶形皮损,累及约 25-30%的体表,大的糜烂伴黏膜病变和尼氏征阳性。最初临床疑似中毒性表皮坏死松解症(TEN),并考虑到最近文献中这些病例成功使用依那西普,我们给予她单次剂量的这种抗肿瘤坏死因子(anti-TNF)药物。随后,皮疹进展停止,皮损在几天内消退。后来,组织病理学显示表皮下水疱,伴密集中性粒细胞浸润,以及在表皮基底膜带线状沉积免疫球蛋白 A(IgA),从而明确诊断为药物诱导的类似 TEN 的线性 IgA 皮肤病。线性 IgA 皮肤病可表现为严重的临床表现,甚至类似 TEN,且死亡率高,尤其是药物诱导的病例。我们在英文文献中未发现任何其他用依那西普治疗线性 IgA 皮肤病的报道。抗 TNF 药物可能是这种皮肤病的有用治疗选择。