De Andrade Francisco Assis, Giavedoni Priscila, Keller Johannes, Sainz-de-la-Maza Maria Tereza, Ferrando Juan
Ophthalmology Department, Hospital Clínic de Barcelona, School of Medicine, Universitat de Barcelona, Barcelona, Catalonia, Spain,
Immunol Res. 2014 Dec;60(2-3):356-60. doi: 10.1007/s12026-014-8602-4.
Alopecia areata is understood as an autoimmune disease T cell-mediated mainly involving hair follicles in humans. It is a multifactorial aetiologic disease characterised by non-scarring alopecia and asymptomatic areas, affecting approximately 2 % of dermatology patients. Recent studies suggest that the pathogenesis of AA plays an important role in the association of certain HLA groups, neuroendocrine parameters and immunogenic factors. During 3 months (March to May 2013) at Hospital Clínic de Barcelona, 22 patients with severe alopecia areata underwent ophthalmic examination to determine whether there were ocular findings in the following parameters: Best-corrected visual acuity on decimal Snellen optotype, anterior segment slit-lamp examination and photograph, intraocular pressure measurement and dilated fundoscopy. Ultra-wide-field retinal imaging with or without red-free photograph was carried out with the Optomap 200 Tx (Optos, DunFermline, UK). Forty-four eyes of 22 patients were analysed [15 females (68.2 %)]. The mean age was 38.9 (SD 13.7) and mean time of evolution was 19.9 years (SD 16.3). Alopecia areata clinical patterns were multifocal [n = 10 (45.5 %)], universalis [n = 7 (31.8 %)], totalis [n = 3 (13.6 %)] and focal [n = 2 (9.1 %)]. Best-corrected visual acuity was 1.0 in almost all patients, but only three eyes (6.8 %) had vision of 0.7. Ocular findings were as follows: madarosis [n = 7 partial loss of eyelashes (31.85 %) and n = 4 total loss (18.2 %)], lens changes [n = 4 (18.2 %)], cataract [n = 3 (13.65 %)]. Ultra-wide fundus photography examination showed peripheral drusen [n = 17 eyes (38.6 %)], white-without-pressure changes [n = 8 eyes (18.22 %)] and peripheral retinal degenerations [n = 3 eyes (6.81 %)]. Ocular findings in patients with alopecia areata are reported and discussed by dermatologic and ophthalmic evaluation.
斑秃被认为是一种主要由T细胞介导的自身免疫性疾病,主要累及人类毛囊。它是一种多因素病因的疾病,其特征为非瘢痕性脱发和无症状区域,约2%的皮肤科患者受其影响。最近的研究表明,斑秃的发病机制在某些HLA组、神经内分泌参数和免疫原性因素的关联中起着重要作用。2013年3月至5月期间,在巴塞罗那临床医院,22例重度斑秃患者接受了眼科检查,以确定在以下参数方面是否存在眼部表现:使用十进制斯内伦视力表的最佳矫正视力、前段裂隙灯检查及拍照、眼压测量和散瞳眼底检查。使用Optomap 200 Tx(Optos公司,英国邓弗姆林)进行超广角视网膜成像,有无无赤光照片均可。对22例患者的44只眼进行了分析[15例女性(68.2%)]。平均年龄为38.9岁(标准差13.7),平均病程为19.9年(标准差16.3)。斑秃的临床类型为多灶性[n = 10例(45.5%)]、普秃[n = 7例(31.8%)]、全秃[n = 3例(13.6%)]和局限性[n = 2例(9.1%)]。几乎所有患者的最佳矫正视力均为1.0,但只有3只眼(6.8%)视力为0.7。眼部表现如下:睫毛脱落[n = 7例部分睫毛缺失(31.85%)和n = 4例全部缺失(18.2%)]、晶状体改变[n = 4例(18.2%)]、白内障[n = 3例(13.65%)]。超广角眼底摄影检查显示周边玻璃膜疣[n = 17只眼(38.6%)]、无压白变[n = 8只眼(18.22%)]和周边视网膜变性[n = 3只眼(6.81%)]。通过皮肤科和眼科评估报告并讨论了斑秃患者的眼部表现。