具有潜在治疗效果的胶原基生物材料

IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL
R. Nedelcuță, G. Călin, M. Nedelcuţă, V. Băleanu, D. Davițoiu, B. Socea, B. Stănoiu
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引用次数: 0

摘要

大疱性表皮松解症(EB)是一种罕见、严重的遗传性疾病,目前尚无治愈方法。除了最初的定义外,后来对该疾病的定义有所放宽,包括该实体中的中毒性表皮坏死松解症和Stevens-Johnson综合征的表现。在医学实践中,有些病例与文献中的描述不重叠,因此治疗必须根据具体情况进行调整和个性化。我们介绍了一例女性新生儿,其早发性产前表皮松解症的“从头”突变和我们的个性化治疗管理,基于通过酶过程从牛角膜中提取的胶原蛋白。组织学检查显示,胶原膜充当48小时后形成表面单层的上皮细胞的支撑。因此该病例报告表明,基于胶原蛋白的生物材料可用于加速儿童各种情况下的真皮表皮愈合,如Stevens-Johnson综合征、大疱性表皮松解症和大面积烧伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Collagen-based biomaterials with possible therapeutic effects
Epidermolysis bullosa (EB) is a rare, serious genetic disease, incurable through the current means. Apart from this initial definition, there was later some ease in the definition of the disease, including the manifestations of toxic epidermal necrolysis and Stevens Johnson syndrome in this entity. In medical practice, there are cases that do not overlap with the description in the literature, thus the treatment must be adapted and personalized to the particularities. We present the case of a female new-born, with "de novo" mutation for the early-onset antenatal epidermolysis and our personalized therapeutic management, based on collagen from bovine corneas by enzymatic process. The histological examination showed that the collagen membranes serve as a support for the epithelial cells that formed a surface monolayer after 48 hours. Therefore. this case report shows that collagen-based biomaterials could be used to accelerate the dermal-epidermal healing in various conditions of the child, such as Stevens Johnson syndrome, bullous epidermolysis and widespread burns.
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来源期刊
Journal of Mind and Medical Sciences
Journal of Mind and Medical Sciences MEDICINE, GENERAL & INTERNAL-
自引率
61.10%
发文量
37
审稿时长
8 weeks
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