组织工程真皮微脂肪组织与人工真皮用于皮肤癌切除术后面部重建的比较。

IF 3.7 3区 医学 Q2 ENGINEERING, BIOMEDICAL Bioengineering Pub Date : 2025-02-03 DOI:10.3390/bioengineering12020145
Kyu-Il Lee, Won-Seok Song, Seung-Kyu Han, Kyung-Chul Moon, Seong-Ho Jeong, Eun-Sang Dhong
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引用次数: 0

摘要

我们的团队先前已经证明,组织工程真皮含有培养成纤维细胞或脂肪来源的基质血管部分细胞,在覆盖面部缺陷的疤痕质量方面优于人工真皮。然而,将这些细胞用于临床需要食品和药物管理局的批准,并且涉及复杂的细胞培养或分离程序。本回顾性研究旨在比较含有微脂肪组织(MAT)的组织工程真皮和人工真皮在面部重建中的效果。在人工真皮上植入由MAT组成的组织工程真皮30例,未植入MAT的人工真皮35例。评估愈合后一年瘢痕收缩、颜色不匹配、地标扭曲的愈合时间和严重程度。组织工程真皮组创面再生时间为30.0±4.3 d,而人工真皮组创面再生时间为34.3±5.4 d (p < 0.05)。组织工程真皮组dE2000平均评分为4.9±1.7分,人工真皮组为5.1±1.7分(p = 0.57)。组织工程真皮组瘢痕收缩程度为16.2±12.3%,人工真皮组为23.2±12.8% (p < 0.05)。组织工程真皮组和人工真皮组的地标性变形严重等级分别为0.20±0.50和0.50±0.71,差异有统计学意义(p < 0.05)。这些发现表明,在愈合时间、疤痕收缩和标志性变形严重程度方面,含有MAT的组织工程真皮移植物优于人工真皮移植物用于面部重建。然而,两组之间的颜色不匹配没有显着差异。
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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Comparison of Tissue-Engineered Dermis with Micronized Adipose Tissue and Artificial Dermis for Facial Reconstruction Following Skin Cancer Resection.

Our group has previously demonstrated that tissue-engineered dermis containing cultured fibroblasts or adipose-derived stromal vascular fraction cells is superior to artificial dermis in terms of scar quality for covering facial defects. However, using these cells for clinical applications requires Food and Drug Administration approval and involves complex procedures for cell culture or isolation. This retrospective study aimed to compare effects of tissue-engineered dermis containing micronized adipose tissue (MAT) and artificial dermis for facial reconstruction. Tissue-engineered dermis consisting of MAT seeded on artificial dermis was applied in 30 cases, while artificial dermis without MAT was grafted in 35 cases. Healing time and severities of scar contraction, color mismatch, and landmark distortion at one year after healing were evaluated. Wounds in the tissue-engineered dermis group re-epithelialized in 30.0 ± 4.3 days compared to 34.3 ± 5.4 days in the artificial dermis group (p < 0.05). The average dE2000 score in color mismatch analysis was 4.9 ± 1.7 in the tissue-engineered dermis group and 5.1 ± 1.7 in the artificial dermis group (p = 0.57). The extent of scar contraction was 16.2 ± 12.3% in the tissue-engineered dermis group and 23.2 ± 12.8% in the artificial dermis group (p < 0.05). The average severity grade of landmark distortion was 0.20 ± 0.50 in the tissue-engineered dermis group and 0.50 ± 0.71 in the artificial dermis group (p < 0.05). These findings indicate that tissue-engineered dermis grafts containing MAT are superior to artificial dermis grafts for facial reconstruction in terms of healing time, scar contraction, and landmark distortion severity. However, there was no significant difference in color mismatch between the two groups.

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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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