Aviv Barzilai, Yaron Zafrir, Anat Achiron, Sharon Baum
Department of Dermatology, Sheba Medical Center, Tel-Hashomer, Ramat-Gan Affiliated to The Sackler Faculty of Medicine, Tel Aviv University Tel Aviv, Israel.
Institute of Pathology, Sheba Medical Center, Tel-Hashomer, Ramat-Gan Affiliated to The Sackler Faculty of Medicine, Tel Aviv University Tel Aviv, Israel.
Int J Clin Exp Pathol. 2018 Jun 1;11(6):3126-3133. eCollection 2018.
Multiple sclerosis (MS) is a chronic demyelinating disease of the central nervous system. Glatiramer acetate (GA) is a commonly used immunomodulating drug. It is administered subcutaneously and is usually well tolerated; however, various local site reactions have been documented. To characterize the clinical and histopathological patterns of local site reactions in patients treated with GA. A retrospective case series of 12 patients with MS who experienced a local site reaction following treatment with GA. We recognized 3 distinctive clinical patterns: early lesions with erythematous urticarial plaques and nodules (EPN) (75%), and late lesions: lipoatrophy (16.6%) and morpheiform plaques (8.4%). Biopsies revealed that the EPN lesions were characterized by superficial and deep infiltrate with eosinophils and some neutrophils, while the lipoatrophy showed sparse chronic inflammatory infiltrate with delicate fibrosis. The morpheiform plaque showed mixed inflammatory infiltrate and fibrosis. Seven patients applied clobetasole propionate ointment and then switched to tacrolimus monohydrate 0.1% ointment for up to a month. This treatment was beneficial for all patients with EPN. GA can cause a spectrum of injection site reactions that can be classified into 3 distinct patterns based on their time frame, clinical picture and histological pattern. Topical treatment with a potent steroid and tacrolimus cream can alleviate the EPN response.
多发性硬化症(MS)是一种中枢神经系统的慢性脱髓鞘疾病。醋酸格拉替雷(GA)是一种常用的免疫调节药物。它通过皮下给药,通常耐受性良好;然而,各种局部部位反应已有记录。为了描述接受GA治疗的患者局部部位反应的临床和组织病理学模式。对12例接受GA治疗后出现局部部位反应的MS患者进行回顾性病例系列研究。我们识别出3种不同的临床模式:早期病变为红斑性荨麻疹斑块和结节(EPN)(75%),以及晚期病变:脂肪萎缩(16.6%)和线状斑块(8.4%)。活检显示,EPN病变的特征是浅层和深层有嗜酸性粒细胞和一些中性粒细胞浸润,而脂肪萎缩表现为稀疏的慢性炎症浸润伴细微纤维化。线状斑块表现为混合性炎症浸润和纤维化。7例患者应用丙酸氯倍他索软膏,然后改用0.1%的一水合他克莫司软膏,持续使用长达1个月。这种治疗对所有EPN患者均有益。GA可引起一系列注射部位反应,根据其时间框架、临床表现和组织学模式可分为3种不同模式。强效类固醇和他克莫司乳膏的局部治疗可减轻EPN反应。