肉毒杆菌毒素A注射液治疗增生性瘢痕和瘢痕疙瘩的临床和组织病理学评价

S. Elfiky, H. Shokeir, M. Elbasiouny, N. Samy
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引用次数: 0

摘要

背景:肥厚性疤痕和瘢痕疙瘩的治疗方法多种多样。并非所有的治疗方式都经过了充分的测试。最近,有研究表明A型肉毒毒素(BTX)对伤口愈合有积极的影响,因此它可能有助于治疗HTS和瘢痕疙瘩。目的探讨BTX单药治疗HTS和瘢痕疙瘩的临床及组织病理学效果。患者与方法对30例HTS合并瘢痕疙瘩患者,采用病灶内注射BTX单药治疗。每个病灶注射BTX (5 IU/cm2,每4周1次,共4次)。治疗前后对病变进行免疫组化评价。治疗前后进行温哥华疤痕评分及临床影像学检查。结果BTX治疗后表皮厚度(P=0.001)和成纤维细胞真皮面积% (P=0.001)均有显著性差异。此外,治疗后温哥华疤痕评分显著下降(P<0.001)。结论BTX注射治疗HTS和瘢痕疙瘩是一种有效且耐受性良好的治疗方法,可对HTS和瘢痕疙瘩的成纤维细胞活性产生影响。
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Clinical and histopathological assessment of botulinum toxin-A injection for treatment of hypertrophic scars and keloids
Background Various treatments for hypertrophic scars (HTS) and keloids are available. Not all treatment modalities have been adequately tested. Recently, it has been shown that botulinum toxin type A (BTX) positively affects wound healing, so it might contribute in treating HTS and keloids. Objective To assess the effect of BTX intralesional injection as a monotherapy for the treatment of HTS and keloids clinically and histopathologically. Patients and methods A total of 30 patients with HTS and keloids were treated by intralesional injection of BTX as a monotherapy. Each lesion was injected with BTX (5 IU/cm2 once every 4 weeks for four sessions). Immunohistochemical evaluation of the lesions before and after treatment was done. Moreover, Vancouver scar scale and clinical imaging were taken before and after treatment. Results There was a highly significant difference after treatment with BTX intralesional in both the epidermal thickness (P=0.001) and area% of fibroblast dermis (P=0.001). Additionally, there was a significant decline in Vancouver scar scale after treatment (P<0.001). Conclusion BTX injection of HTS and keloids can be considered as a promising effective and well tolerated therapeutic option acting on fibroblast activity of HTS and keloids.
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来源期刊
CiteScore
0.50
自引率
0.00%
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0
审稿时长
17 weeks
期刊介绍: The Journal of The Egyptian Women''s Dermatologic Society (JEWDS) was founded by Professor Zenab M.G. El-Gothamy. JEWDS is published three times per year in January, May and September. Original articles, case reports, correspondence and review articles submitted for publication must be original and must not have been published previously or considered for publication elsewhere. Their subject should pertain to dermatology or a related scientific and technical subject within the field of dermatology.
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