Meythaler H, Flick K
Klin Monbl Augenheilkd. 1976 Jul;169(1):100-4.
A description is given of a 37-year-old man, who suffered from a IgG myelom, diagnosed by internal medicine. The initial symptoms of the disease were grey-white, crystalline deposits in the cornea and recurring inflammation of the iris in both eyes. Only when a multiple recurring exophthalmos occurred, could the diagnosis be determined through an intensive internal examination. The continuing disease was still complicated by an insufficiency of the kidneys with hypertony and beginning retinopathia angiospastica.
本文描述了一名37岁男性，他患有IgG型骨髓瘤，由内科诊断。该疾病的初始症状是角膜出现灰白色结晶沉积物以及双眼虹膜反复发炎。只有当出现多次反复性眼球突出时，才能通过全面的内科检查确定诊断。该疾病的持续发展仍伴有肾功能不全、高血压以及早期血管痉挛性视网膜病变等并发症。
