毛囊单位提取毛发移植供体部位愈合:现有证据、细胞机制和未来研究方向。

Ney Arencibia Pérez, María José Guerrero Roldán
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引用次数: 0

摘要

毛囊单位提取(FUE)已成为头发移植的主要技术,但对供体区域的最佳管理仍然是一个临床挑战。本系统综述分析了FUE毛发移植术中和术后对供体区域的干预措施,重点关注临床结果以及组织修复、炎症反应和再生过程中涉及的细胞和分子机制。在PubMed和EMBASE上进行了全面的文献检索(2000年1月- 2025年6月),确定了评估供体区域治疗的临床研究,并报告了与愈合、炎症、感染和患者满意度相关的结果。四项研究符合纳入标准,包括皮质类固醇浸润、富血小板血浆(PRP)、术后护理时机和毛囊源性微组织(HFMT)应用。有证据表明,术中使用皮质类固醇可显著减少术后水肿,可能是通过调节局部炎症途径和血管通透性。术后早期伤口护理与毛囊炎发病率降低有关,这突出了及时干预在预防微生物定植和免疫反应失调中的重要性。虽然PRP和HFMT显示出促进细胞增殖和加速伤口愈合的潜力,但目前的数据受到研究设计异质性和缺乏标准化分子终点的限制。该综述确定了在探索供体区域愈合的细胞动力学机制研究中的一个关键空白,包括角化细胞、成纤维细胞和免疫细胞的作用。未来的研究需要结合分子生物标志物和先进的成像来阐明驱动最佳组织再生的途径。这些见解可以为基于证据的方案提供信息,不仅可以改善临床结果,还可以促进我们对FUE背景下头皮伤口生物学的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Donor site healing in follicular unit extraction hair transplantation: current evidence, cellular mechanisms, and future research directions.

Follicular unit extraction (FUE) has become a leading technique in hair transplantation, yet optimal management of the donor area remains a clinical challenge. This systematic review analyzes intraoperative and postoperative interventions applied to the donor area in FUE hair transplantation, with a focus on both clinical outcomes and the cellular and molecular mechanisms involved in tissue repair, inflammatory response, and regenerative processes. A comprehensive literature search was conducted in PubMed and EMBASE (January 2000-June 2025), identifying clinical studies that evaluated donor area treatments and reported outcomes related to healing, inflammation, infection, and patient satisfaction. Four studies met the inclusion criteria, encompassing corticosteroid infiltration, platelet-rich plasma (PRP), timing of postoperative care, and hair follicle-derived microtissue (HFMT) application. Evidence suggests that intraoperative corticosteroid use significantly reduces postoperative edema, likely by modulating local inflammatory pathways and vascular permeability. Early postoperative wound care is associated with decreased folliculitis incidence, highlighting the importance of timely intervention in preventing microbial colonization and dysregulated immune responses. While PRP and HFMT show potential for enhancing cellular proliferation and accelerating wound closure, current data are limited by heterogeneity in study design and lack of standardized molecular endpoints. The review identifies a critical gap in mechanistic studies exploring the cellular dynamics of donor area healing, including the roles of keratinocytes, fibroblasts, and immune cells. Future research integrating molecular biomarkers and advanced imaging is needed to elucidate the pathways driving optimal tissue regeneration. These insights may inform evidence-based protocols that not only improve clinical outcomes but also advance our understanding of scalp wound biology in the context of FUE.

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