Safety and efficacy of interstitial bleomycin sclerotherapy for foam sclerosant-infeasible small solid venous malformations in the lower extremity.

Kyoung Yeon Lee, Taejun Jeon, Sang Yub Lee, Kwang Bo Park, Hong Suk Park, Dongho Hyun, Sung Ki Cho, Sung Wook Shin, Chang Hoon Oh
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Abstract

PurposeTo evaluate the safety and efficacy of interstitial bleomycin sclerotherapy for treating small painful venous malformations (VMs) in the lower extremities.MethodsBetween September 2022 and August 2024, 256 patients underwent 420 sclerotherapy sessions for slow-flow vascular malformations. Exclusions included sponge-form VMs, lymphatic malformations, fibroadipose vascular anomalies, and syndromic vascular anomalies. Thirteen patients with solid VMs in the lower extremities, unresponsive to prior foam sclerotherapy (n = 6) or with vascular access challenges due to the lesion's solid nature (n = 7), underwent 19 interstitial bleomycin sclerotherapy sessions. Pre- and post-treatment assessments included visual analog scale (VAS) scores and imaging findings for lesion diameter and vascularity.ResultsNineteen bleomycin sclerotherapy sessions were conducted in 13 patients. VMs were intramuscular (n = 11), in the sub-fascial fat layer (n = 1), or both (n = 1). The mean interval between prior foam and bleomycin sclerotherapy was 818 days, with a 254-day follow-up after treatment. Pain improved in 92% of patients, with a VAS score reduction from 8.5 to 2.8 (p = .0001). One patient showed no improvement after three sessions. Among six patients with vascularity detected on Doppler ultrasound pre-treatment, all demonstrated resolution post-treatment (p = .0313). Mean diameter reduction of 0.27 cm was not statistically significant (p = .0573). Three minor/moderate adverse events occurred: allergic reactions and skin pigmentation.ConclusionInterstitial bleomycin sclerotherapy is a safe and effective option for reducing pain and vascularity in lower extremity solid VMs unresponsive to foam sclerotherapy or presenting poor vascular access.

博来霉素间质硬化治疗下肢泡沫硬化不可行的小实体静脉畸形的安全性和有效性。
目的评价博来霉素间质硬化治疗下肢小静脉畸形(vm)的安全性和有效性。方法在2022年9月至2024年8月期间,256例慢流血管畸形患者接受了420次硬化治疗。排除包括海绵状vm、淋巴畸形、纤维脂肪血管异常和综合征性血管异常。13例下肢实性vm患者,对先前的泡沫硬化治疗无反应(n = 6)或由于病变的实性而导致血管通路困难(n = 7),接受了19次间质性博来霉素硬化治疗。治疗前和治疗后的评估包括视觉模拟量表(VAS)评分和病变直径和血管分布的影像学结果。结果13例患者共接受博来霉素硬化治疗19次。vm分别位于肌内(n = 11)、筋膜下脂肪层(n = 1)或两者同时存在(n = 1)。先前泡沫和博来霉素硬化治疗的平均间隔时间为818天,治疗后随访254天。92%的患者疼痛得到改善,VAS评分从8.5降至2.8 (p = 0.0001)。一名患者在三次治疗后没有任何改善。6例术前多普勒超声检查发现血管通畅的患者,治疗后均恢复通畅(p = .0313)。平均直径减小0.27 cm无统计学意义(p = .0573)。发生了三个轻微/中度不良事件:过敏反应和皮肤色素沉着。结论对泡沫硬化治疗无反应或血管通路不良的下肢实体vm,间质性博来霉素硬化治疗是一种安全有效的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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