Mayser P
, Hofmannstr. 11, 35444, Biebertal, Deutschland.
Hautarzt. 2016 Sep;67(9):724-31. doi: 10.1007/s00105-016-3844-9.
Based on the technical information that oral terbinafine must be used with caution in patients with pre-existing psoriasis or lupus erythematosus, the literature was summarized. Terbinafine belongs to the drugs able to induce subcutaneous lupus erythematosus (SCLE)-with a relatively high risk. The clinical picture of terbinafine-induced SCLE may be highly variable and can also include erythema exsudativum multiforme-like or bullous lesions. Thus, differentiation of terbinafine-induced Stevens-Johnson syndrome or toxic epidermal necrolysis may be difficult. Therefore, terbinafine should be prescribed with caution in patients who show light sensitivity, arthralgias, positive antinuclear antibodies or have a history of SLE or SCLE. Case reports include wide-spread, but mostly nonlife-threatening courses, which did not require systemic therapy with steroids or antimalarials in every case. Terbinafine is also able to induce or to aggravate psoriasis. The latency period seems to be rather short (<4 weeks). Terbinafine therefore is not first choice if a systemic therapy with antimycotics is indicated in a patient with psoriasis or psoriatic diathesis. Azole derivatives according to the guidelines may be used as an alternative.
基于口服特比萘芬在已有银屑病或红斑狼疮患者中必须谨慎使用的技术信息,对相关文献进行了总结。特比萘芬属于能够诱发皮下红斑狼疮(SCLE)的药物——风险相对较高。特比萘芬诱发的SCLE临床表现可能高度多变,还可能包括多形性渗出性红斑样或大疱性皮损。因此,区分特比萘芬诱发的史蒂文斯-约翰逊综合征或中毒性表皮坏死松解症可能较为困难。所以,对于有光敏感、关节痛、抗核抗体阳性或有系统性红斑狼疮(SLE)或SCLE病史的患者,应谨慎开具特比萘芬处方。病例报告显示病程广泛,但大多不危及生命,并非每个病例都需要使用类固醇或抗疟药进行全身治疗。特比萘芬还能够诱发或加重银屑病。潜伏期似乎相当短(<4周)。因此,对于有银屑病或银屑病素质且需要抗真菌药进行全身治疗的患者,特比萘芬并非首选。根据指南,唑类衍生物可作为替代药物。