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瘢痕治疗的临床进展OA

The advances in scar clinical treatment

中文摘要英文摘要

瘢痕是创伤愈合后常见的异常重塑结果,增生性瘢痕和瘢痕疙瘩可引起疼痛、瘙痒、外观畸形及功能受限,并对患者心理状态和社会回归造成持续影响.瘢痕治疗已由单一局部处理转向以风险分层、早期干预和多模式联合为核心的综合管理.本文围绕瘢痕的临床分类与风险评估、硅酮与压力疗法、减张技术、局部糖皮质激素、5-氟尿嘧啶、博来霉素和A型肉毒毒素注射、血管与剥脱性激光、激光辅助递药、手术联合放射治疗,以及再生医学、外泌体、组织工程和纳米递送等方向进行综述.现有证据提示,硅酮、减张和压力疗法更适合早期预防,局部注射和能量治疗适用于活动性病变的控制,单纯切除因复发率较高通常不宜作为唯一策略.未来研究应强化结局标准化、患者报告结局、长期随访和分子分型指导下的精准治疗.

Scars represent a common outcome of aberrant tissue remodeling following wound healing.The hypertrophic scars and keloids cause pain,pruritus,cosmetic disfigurement,and functional impairment,which carry significant psychological and social consequences for patients.Scar management has shifted from single-modality treatment to a multidisciplinary strategy incorpo-rating risk stratification,early intervention,and multimodal therapy.We reviewed the recent pro-gresses in scar management including clinical guidelines,randomized controlled trials,silicone-based prevention,pressure therapy,tension-reduction techniques,intralesional corticosteroids,5-fluorouracil(5-FU),bleomycin,and botulinum toxin type A(BoNT-A),vascular and ablative laser therapy,laser-assisted drug delivery,surgery combined with adjuvant radiotherapy,and e-merging approaches such as regenerative medicine,exosomes,tissue engineering,and nano-ena-bled delivery et al.Current studies have shown that silicone,tension reduction,and pressure ther-apy are suitable for early prevention;the intralesional and energy-based therapies are suitable for active lesions;and the excision is not the only strategy because of the high recurrence risk.Future investigations are required for precision treatment guided by the standardized outcomes,patient-re-ported measures,long-term follow-up and molecular profiling.

沈非凡;刘悦;宋金鹏;周金辉;司小强

甘肃中医药大学第一临床医学院甘肃中医药大学第一临床医学院甘肃中医药大学第一临床医学院甘肃中医药大学第一临床医学院甘肃省人民医院,甘肃 兰州 730000

瘢痕瘢痕疙瘩增生性瘢痕硅酮制剂激光治疗压力疗法再生医学

scarkeloidhypertrophic scarsilicone preparationlaser therapypressure therapyregenerative medicine

《皮肤性病诊疗学杂志》 2026 (7)

527-535,9

甘肃省自然科学基金(22JR5RA690)

10.3969/j.issn.1674-8468.2026.07.008

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