Vivino F B, Minerva P, Huang C H, Orlin S E
College of Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.
J Rheumatol. 2001 Feb;28(2):379-82.
Corneal melting is a rare complication of S ogren's syndrome (SS). Previously reported cases of corneal ulceration occurred in patients with established SS, usually secondary to RA. We describe the first case of corneal ulceration with stromal melting as the initial presentation of primary SS. A 79-year-old man without prior sicca symptoms developed a large sterile corneal ulcer that required extensive treatment over several months with ocular lubricants, systemic immunosuppressives, and surgical repair. Evaluation for an underlying connective tissue disease revealed positive antinuclear antibodies (1:640 speckled) and anti-SSA antibody. A lip biopsy established the diagnosis of SS. Ulceration later occurred in the contralateral eye. Two years after the last corneal ulcer and no longer taking prednisone, the patient's ocular disease remained quiescent taking azathioprine 175 mg and hydroxychloroquine 400 mg daily. This case highlights the potential for primary SS to present with serious ocular complications despite lack of a priori sicca symptoms, as well as the importance of immunosuppressive therapy in the treatment of this complication.
角膜溶解是干燥综合征(SS)的一种罕见并发症。先前报道的角膜溃疡病例发生在已确诊的SS患者中,通常继发于类风湿关节炎(RA)。我们描述了首例以角膜基质溶解为首发表现的原发性SS角膜溃疡病例。一名79岁男性,此前无干眼症状,出现了一个巨大的无菌性角膜溃疡,需要在数月内使用眼部润滑剂、全身免疫抑制剂及手术修复进行广泛治疗。对潜在结缔组织病的评估显示抗核抗体阳性(1:640,斑点型)及抗SSA抗体阳性。唇腺活检确诊为SS。随后对侧眼也发生了溃疡。在最后一次角膜溃疡发作两年后,患者不再服用泼尼松,目前每日服用硫唑嘌呤175mg及羟氯喹400mg,眼部疾病处于静止状态。该病例凸显了原发性SS即便缺乏先验性干眼症状也可能出现严重眼部并发症的可能性,以及免疫抑制治疗在该并发症治疗中的重要性。