Ophthalmic manifestations in patients with collagen vascular disorders: a hospital-based retrospective observational study

被引:4
|
作者
Sharma, Surinder Kumar [1 ]
Sharma, Anju Lath [2 ]
Mahajan, Vikram K. [3 ]
机构
[1] Mobile Eye Ctr, Kangra 176215, Himachal Prades, India
[2] Zonal Hosp, Dept Dermatol Venereol & Leprosy, Kangra 176215, Himachal Prades, India
[3] Dr Rajendra Prasad Govt Med Coll, Dept Dermatol Venereol & Leprosy, Kangra Tanda 176001, Himachal Prades, India
关键词
Autoimmune disorders; Blepharitis; Dermatomyositis; Discoid lupus erythematosus; Keratopathy; Lupus erythematosus; Ocular abnormalities; Ocular surface disease; Retinopathy; Sjö gren' s syndrome; Systemic sclerosis; Uveitis;
D O I
10.1007/s10792-021-01833-x
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Aim To study frequency and characteristics of ocular manifestations in Indian patients with collagen vascular disorders. Methods The medical records of 73 patients (Males: Females 16:57) aged between 22 and 78 years (mean +/- SD = 43.5 +/- 12.9 years) with collagen vascular diseases were analyzed retrospectively for demography, subtypes of collagen vascular disease, and findings of complete ophthalmic examination. Results Lupus erythematosus (LE) in 39(53.4%, (SLE 18, DLE 21), systemic sclerosis in 27(37%), dermatomyositis in 5(6.8%), and primary Sjogren's syndrome in 2(2.7%) patients, respectively, were observed. Only 35(47.9%) patients had ocular manifestations. In LE keratoconjunctivitis sicca (n = 6), keratitis (n = 5), severe blepharitis (n = 3), retinopathy (n = 2), and optic neuritis in one patient, respectively, were major ocular manifestations. Major abnormalities occurring in systemic sclerosis included restricted eyelid mobility of variable severity (n = 8), eyelid telangiectasia (n = 5), keratoconjunctivitis sicca (n = 6), cataract (n = 5), shallow fornices (n = 4), conjunctival surface disease (n = 4), and uveitis, keratitis, episcleritis in one patient each, respectively. One patient with dermatomyositis had heliotrope rash. Two patients with primary Sjogren's syndrome had keratoconjunctivitis sicca. Conclusions The study shows that LE frequently presented with keratoconjunctivitis sicca, retinopathy, and optic neuritis. Systemic sclerosis commonly develops eyelid immobility, blepharitis and telangiectasia, ocular surface disease and keratoconjunctivitis sicca, corneal abnormalities, and uveitis. A comprehensive ocular evaluation is imperative for early detection and management particularly of ocular surface disease, uveitis, and retinopathy to prevent potential sight-threatening complications. Limitations include retrospective study design and small number of patients for stratification.
引用
收藏
页码:2765 / 2775
页数:11
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