Waki E Y, Crumley R L, Jakowatz J G
Division of Otolaryngology-Head and Neck Surgery, University of California.
Arch Otolaryngol Head Neck Surg. 1991 Oct;117(10):1177-81. doi: 10.1001/archotol.1991.01870220125023.
The treatment of keloids remains difficult. In experimental studies, lathyrogenic agents and colchicine have been shown to be effective in keloid prevention. Recently, a study was published of a new animal model utilizing human keloids implanted in athymic mice. We used the same model to compare the effects of penicillamine, acetylcysteine, colchicine, and triamcinolone acetonide. Unexpectedly, all keloids implanted showed a growth peak at 4 weeks and then regression in size. Histologic sections of the implanted keloids revealed peripheral vascularity, collagen bundles similar to the parent keloids, and no evidence of implant rejection. After 8 weeks, the mice treated with the lathyrogenic agents exhibited a higher rate of regression when compared with the control mice. While triamcinolone acetonide may have prevented keloid implant growth, drug toxic reaction may have been a factor.
瘢痕疙瘩的治疗仍然很困难。在实验研究中,致纤维化剂和秋水仙碱已被证明对预防瘢痕疙瘩有效。最近,一项关于利用植入无胸腺小鼠体内的人类瘢痕疙瘩建立新动物模型的研究发表了。我们使用相同的模型比较了青霉胺、乙酰半胱氨酸、秋水仙碱和曲安奈德的效果。出乎意料的是,所有植入的瘢痕疙瘩在4周时出现生长高峰,然后尺寸缩小。植入瘢痕疙瘩的组织学切片显示外周血管形成、胶原束与原瘢痕疙瘩相似,且无植入排斥迹象。8周后,与对照小鼠相比,用致纤维化剂治疗的小鼠瘢痕疙瘩缩小率更高。虽然曲安奈德可能阻止了瘢痕疙瘩植入物的生长,但药物毒性反应可能是一个因素。