Mizutani H, Yoshida T, Nouchi N, Hamanaka H, Shimizu M
Department of Dermatology, Mie University, Faculty of Medicine, Japan.
J Dermatol. 1999 Jan;26(1):11-7. doi: 10.1111/j.1346-8138.1999.tb03502.x.
Four patients with systemic scleroderma (SSc), 4 patients with morphea, and 4 patients with hypertrophic scar were treated with topical tocoretinate for 6 months to 3 years and studied clinically and histopathologically. Clinically, all of the lesions responded to this therapy. The stiffness of the skin lesions, glossy appearance of the lesions, and telangiectasia improved. Histopathologically, the proliferated collagen fibers decreased in thickness, and the inter-fiber spaces increased. Immunoreactive tenascin-C expressed in the proliferated deep dermal fibers of the SSc and hypertrophic scar lesions was markedly decreased compared with the level before the topical tocoretinate therapy. Topical tocoretinate has been used for the treatment of ulcers; it is also a potent treatment for sclerotic skin diseases.
对4例系统性硬化症(SSc)患者、4例硬斑病患者和4例肥厚性瘢痕患者外用托瑞维甲酸治疗6个月至3年,并进行临床和组织病理学研究。临床上,所有病变对该治疗均有反应。皮肤病变的僵硬程度、病变的光泽外观和毛细血管扩张均有所改善。组织病理学上,增生的胶原纤维厚度减小,纤维间间隙增大。与外用托瑞维甲酸治疗前相比,SSc和肥厚性瘢痕病变增生的真皮深层纤维中表达的免疫反应性肌腱蛋白-C明显减少。外用托瑞维甲酸已用于治疗溃疡;它也是治疗硬化性皮肤病的有效方法。