Department and Institute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei, Taiwan; Department of Dermatology, Wan Fang Hospital, Taipei Medical University Hospital, Taipei, Taiwan.
Department of Dermatology, Drug Hypersensitivity Clinical and Research Center, Chang Gung Memorial Hospital, Linkou, Taipei, and Keelung, Taiwan; College of Medicine, Chang Gung University, Taoyuan, Taiwan.
J Am Acad Dermatol. 2017 Aug;77(2):247-255.e2. doi: 10.1016/j.jaad.2017.02.021. Epub 2017 May 10.
Methotrexate-induced epidermal necrosis (MEN) is a rare but life-threatening cutaneous reaction that mimics Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN).
To investigate the clinicopathology, risk factors, and prognostic factors of MEN.
We enrolled 24 patients with MEN and 150 controls and analyzed the demographics, pathology, and plasma concentrations of methotrexate (MTX).
Patients with MEN showed extensive skin necrosis (mean, 33.2% total body surface area) but no target lesions. The histopathology displayed keratinocyte dystrophy. Early signs of MEN included painful skin erosions, oral ulcers, and leukopenia/thrombocytopenia. Although 79.2% patients received leucovorin treatment, there was 16.7% mortality. Risk factors for MEN included older age (>60 years), chronic kidney disease, and high initial dosage of MTX without folic acid supplementation. Renal insufficiency delayed MTX clearance. Severe renal disease and leukopenia predicted poor prognosis in MEN, but none of the SCORe of Toxic Epidermal Necrosis criteria were associated with mortality of MEN.
The study was limited by the small sample size.
MEN exhibited distinct clinicopathologic features from SJS/TEN. Recognition of the early signs and prognostic factors is important, because the rapid institution of leucovorin may be helpful. To reduce the risk of MEN, physicians should avoid prescribing MTX to high-risk patients and titrate the dosage slowly upward with folic acid supplementation.
甲氨蝶呤诱导的表皮坏死(MEN)是一种罕见但危及生命的皮肤反应,类似于史蒂文斯-约翰逊综合征(SJS)和中毒性表皮坏死松解症(TEN)。
研究 MEN 的临床病理、危险因素和预后因素。
我们纳入了 24 例 MEN 患者和 150 例对照,并分析了人口统计学、病理学和甲氨蝶呤(MTX)的血浆浓度。
MEN 患者表现为广泛的皮肤坏死(平均 33.2%总体表面积),但无靶病变。组织病理学显示角质形成细胞营养不良。MEN 的早期表现包括疼痛性皮肤糜烂、口腔溃疡和白细胞减少/血小板减少。尽管 79.2%的患者接受了亚叶酸钙治疗,但仍有 16.7%的死亡率。MEN 的危险因素包括年龄较大(>60 岁)、慢性肾脏病和初始 MTX 剂量高而未补充叶酸。肾功能不全可延迟 MTX 清除。严重的肾脏疾病和白细胞减少症预示着 MEN 的预后不良,但毒性表皮坏死松解症评分标准中的任何一项都与 MEN 的死亡率无关。
该研究受到样本量小的限制。
MEN 与 SJS/TEN 的临床病理特征明显不同。认识早期征象和预后因素很重要,因为迅速给予亚叶酸钙可能会有所帮助。为了降低 MEN 的风险,医生应避免给高危患者开 MTX,并在补充叶酸的情况下缓慢滴定剂量。