通过注射富含血小板的纤维蛋白基质诱导皮肤胶原、血管生成和脂肪生成。

Archives of Facial Plastic Surgery Pub Date : 2012-03-01 Epub Date: 2011-10-17 DOI:10.1001/archfacial.2011.784
Anthony P Sclafani, Steven A McCormick
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引用次数: 81

摘要

目的:探讨自体富血小板纤维蛋白基质(PRFM)对皮肤组织的影响。方法:选取4名健康成人志愿者。利用专有系统(Selphyl;审美因素,韦恩,新泽西)并注射到受试者上臂的深层真皮和直接真皮下。在10周的时间内,从治疗区域采集全层皮肤活检标本,并对标本进行组织学评估。结果:组织学检查结果支持临床观察。早在治疗后7天,就观察到活化的成纤维细胞和新的胶原沉积,并在整个研究过程中持续明显。第19天观察到新血管的形成;同时,也注意到皮内脂肪细胞的聚集和皮下脂肪细胞的刺激。这些发现在研究期间变得更加明显,尽管成纤维细胞的反应变得不那么明显。在任何时间点均未观察到异常的有丝分裂图形,仅在研究的最早时间点观察到非常轻微的慢性炎症反应。结论:将PRFM注射到皮肤的真皮深层和真皮下,可以刺激许多细胞的变化,这些变化可以被利用。结合先前的体外和体内研究,我们现在对PRFM的细胞效应及其在面部整形手术中的潜在应用有了更清晰的了解。进一步的工作计划更清楚地阐明PRFM在美容和重建手术中的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Induction of dermal collagenesis, angiogenesis, and adipogenesis in human skin by injection of platelet-rich fibrin matrix.

Objective: To evaluate the histological changes induced in human skin by injection of autologous platelet-rich fibrin matrix (PRFM).

Methods: Four healthy adult volunteers were included in the study. Platelet-rich fibrin matrix was prepared from 9 mL of autologous blood using a proprietary system (Selphyl; Aesthetic Factors, Wayne, New Jersey) and injected into the deep dermis and immediate subdermis of the upper arms of subjects. Full-thickness skin biopsy specimens were taken from the treated areas over a 10-week period, and the specimens were processed for histological evaluation.

Results: Findings from histological examination supported the clinical observation of soft-tissue augmentation. As early as 7 days after treatment, activated fibroblasts and new collagen deposition were noted and continued to be evident throughout the course of the study. Development of new blood vessels was noted by 19 days; also at this time, intradermal collections of adipocytes and stimulation of subdermal adipocytes were noted. These findings became more pronounced over the duration of the study, although the fibroblastic response became much less pronounced. No abnormal mitotic figures were observed at any point, and a very mild chronic inflammatory response was noted only at the earliest time points of the study.

Conclusions: Injection of PRFM into the deep dermis and subdermis of the skin stimulates a number of cellular changes that can be harnessed for use. Coupled with prior in vitro and in vivo studies, we now have a much clearer picture of the cellular effects of PRFM and its potential uses in facial plastic surgery. Further work is planned to more clearly elucidate the potential role of PRFM in aesthetic and reconstructive surgery.

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