Mishra Amit V, Cadieux Danielle C, Gjerde Harald, Lewis Darrell R
Department of Ophthalmology, Dalhousie University, Halifax, NS, Canada.
Cornea. 2020 Nov;39(11):1431-1432. doi: 10.1097/ICO.0000000000002317.
To report a case of peripheral ulcerative keratitis secondary to atypical hemolytic uremic syndrome.
We report the case of a 76-year-old man who presented with bilateral aggressive peripheral ulcerative keratitis. Clinical examinations and investigations are reported from the patients' admission.
The patient had an extended workup for autoimmune and infectious etiologies that all returned negative. The laboratory work in conjunction with renal biopsy and clinical symptoms were consistent with atypical hemolytic uremic syndrome. The patient was treated with systemic steroids for his peripheral ulcerative keratitis and underlying systemic disease. Corneal glueing and amniotic membrane grafting was also performed.
To our knowledge, we report the first known case of peripheral ulcerative keratitis secondary to atypical hemolytic uremic syndrome. In cases where the standard workup is negative, this diagnosis should be considered because it can have significant systemic morbidity.
报告一例继发于非典型溶血尿毒综合征的周边溃疡性角膜炎病例。
我们报告了一名76岁男性患者,其患有双侧侵袭性周边溃疡性角膜炎。报告了患者入院时的临床检查和各项调查情况。
患者针对自身免疫和感染病因进行了全面检查,结果均为阴性。实验室检查结果结合肾活检及临床症状与非典型溶血尿毒综合征相符。患者接受了全身类固醇治疗以治疗其周边溃疡性角膜炎及潜在的全身性疾病。还进行了角膜粘连和羊膜移植手术。
据我们所知,我们报告了首例已知的继发于非典型溶血尿毒综合征的周边溃疡性角膜炎病例。在标准检查结果为阴性的病例中,应考虑这一诊断,因为它可能导致严重的全身性发病。