Inafuku Hisashi, Kasem Khan Mohammed Abul, Nagata Tomoko, Nonaka Shigeo
Division of Dermatology, Organ-oriented Medicine, School of Medicine, Faculty of Medicine, University of the Ryukyus, Okinawa, Japan.
J Dermatol. 2004 Aug;31(8):671-7. doi: 10.1111/j.1346-8138.2004.tb00575.x.
We report a case treated with interferon beta-1b for multiple sclerosis (MS), who developed severe cutaneous ulcers after six months of therapy. Interferon beta-1b had been used in a regimen of 8 million IU administered subcutaneously through oblique direction of the needle, twice a week. The cutaneous ulcers developed at inoculation sites, as a result of penetration of interferon beta into dermis. Other underlying diseases of coagulative or bleeding disorders or secondary infection were excluded. Histological features of non-specific inflammatory reactions including hyperplastic changes of blood vessels without any evidence of vasculitis were the prominent features in this case. Corticosteroid and interferon beta-1b therapy was continued on restricted sites on the extremities with care not to repeat injections at the same sites previously used. The administration of interferon beta into subcutaneous fatty tissues vertically reduced the incidence of dermal penetration of drug and occurrence of ulcerations in this patient. We review other case reports of severe cutaneous reactions associated with interferon beta-1b therapy in MS patients and conclude that local cytokine-mediated, adverse, immune reaction or non-specific cutaneous inflammatory reaction to interferon beta-1b initiated the skin ulceration long after institution of therapy at the injection sites, and the reaction might be related to the depth of injection.
我们报告了一例使用β-1b干扰素治疗多发性硬化症(MS)的患者,该患者在治疗六个月后出现了严重的皮肤溃疡。β-1b干扰素采用每周两次、每次800万国际单位的剂量,通过针头倾斜方向皮下注射给药。皮肤溃疡在接种部位出现,是由于β-1b干扰素渗透到真皮所致。排除了其他潜在的凝血或出血性疾病或继发感染。该病例的突出组织学特征为非特异性炎症反应,包括血管增生性改变,但无任何血管炎证据。继续在四肢有限部位进行皮质类固醇和β-1b干扰素治疗,注意不在先前使用过的相同部位重复注射。将β-1b干扰素垂直注入皮下脂肪组织,降低了该患者药物真皮渗透的发生率和溃疡的发生。我们回顾了其他MS患者中与β-1b干扰素治疗相关的严重皮肤反应的病例报告,并得出结论,局部细胞因子介导的、对β-1b干扰素的不良免疫反应或非特异性皮肤炎症反应在治疗开始很长时间后在注射部位引发了皮肤溃疡,且该反应可能与注射深度有关。