Haque Waqar M, Mir Mohsin R, Hsu Sylvia
Department of Dermatology, Baylor College of Medicine, Houston, Texas, USA.
Dermatol Online J. 2009 Dec 15;15(12):10.
Vogt-Koyanagi-Harada (VKH) syndrome is an inflammatory condition characterized by bilateral uveitis, vitiligo, poliosis, alopecia, and dysacousia. The syndrome results from a T cell mediated autoimmune attack on melanocytes in genetically susceptible individuals. We present a case of VKH syndrome and propose that the alopecia and poliosis described in the original reports by ophthalmologists could instead be alopecia areata with re-growth of white hair.
伏格特-小柳-原田(VKH)综合征是一种炎症性疾病,其特征为双侧葡萄膜炎、白癜风、白发症、脱发和听觉障碍。该综合征是由T细胞介导的对遗传易感性个体黑素细胞的自身免疫攻击所致。我们报告一例VKH综合征病例,并提出眼科医生最初报告中描述的脱发和白发症可能是斑秃伴白发再生。