Frati Munari A C, Rojas Dosal J A
Bol Med Hosp Infant Mex. 1978 Nov-Dec;35(6):1069-76.
A 13 year-old-boy with poliarticular seronegative juvenile rheumatoid arthritis (JRA) and bilateral scleromalacia perforans is described. Ocular lesions were thought to be seconadry to vasculitis. Improvement was obtained with systemic and local corticosteroid therapy, and with subconjunctival auto-graft of fascia lata. This is the first report in the literature about scleromalacia perforans in JRA.
本文描述了一名患有多关节血清阴性幼年类风湿性关节炎（JRA）和双侧穿孔性巩膜软化症的13岁男孩。眼部病变被认为是血管炎的继发表现。通过全身和局部皮质类固醇治疗以及阔筋膜结膜下自体移植，病情得到改善。这是文献中关于JRA患者穿孔性巩膜软化症的首例报告。
