Agarwal Akash, Bansal Parul, Madhual Subhasree, Panda Maitreyee
Department of Dermatology, Institute of Medical Sciences and SUM Hospital, Bhubaneswar, India.
Clin Exp Dermatol. 2025 Apr 24;50(5):1009-1013. doi: 10.1093/ced/llae554.
In this retrospective study, we evaluated the efficacy and safety of modified intralesional aciclovir for the treatment of recalcitrant palmoplantar and ungual warts in 14 patients (7 men and 7 women) of mean age 24.5 years (SD 8.19). Modified aciclovir (50 mg mL-1) was prepared by mixing 250 mg of lyophilized aciclovir powder with 4 mL of distilled water and 1 mL of 2% lignocaine. Then, this solution was injected into each wart at a dose of 0.1 mL or until blanching occurred. Every 2 weeks, the eschar was pared off and the treatment was repeated until a complete cure was observed, for a maximum of five sessions. After five sessions, 82% (n = 55/67) of warts showed a complete response, and 18% (n = 12/67) showed a partial response. Adverse effects reported included lesional tenderness for 2-3 days following injection in 23% (n = 3/13) of patients. Blistering and nail-plate damage were each seen in one patient. Modifying aciclovir treatment by adding lignocaine resulted in an unaltered concentration of aciclovir while maintaining its efficacy. The efficacy and safety were comparable with those reported for previous studies but with greater patient acceptability.
在这项回顾性研究中,我们评估了改良病灶内注射阿昔洛韦治疗14例(7例男性和7例女性)平均年龄24.5岁(标准差8.19)的顽固性掌跖疣和甲周疣的疗效和安全性。改良阿昔洛韦(50mg/mL)是通过将250mg冻干阿昔洛韦粉末与4mL蒸馏水和1mL 2%利多卡因混合制备而成。然后,将该溶液以0.1mL的剂量注入每个疣体,直至出现变白。每2周削去焦痂并重复治疗,直至观察到完全治愈,最多进行5个疗程。5个疗程后,82%(n=55/67)的疣体显示完全缓解,18%(n=12/67)显示部分缓解。报告的不良反应包括23%(n=3/13)的患者在注射后2 - 3天出现病灶压痛。水疱形成和甲床损伤各有1例患者出现。通过添加利多卡因改良阿昔洛韦治疗,可使阿昔洛韦浓度不变,同时保持其疗效。其疗效和安全性与先前研究报告的相当,但患者接受度更高。