Anterior necrotizing scleritis without inflammation, so called scleromalacia perforans, is a rare, severe eye disorder developing on autoimmune damage of episcleral and scleral performing vessels. It is characterized by the progressive scleral thinning without inflammation. The onset of the disease is insidious, progression is slow and no specific symptoms are observed until discoloration of the sclera is … Click to read full case...
Source: https://journal.medizzy.com/super-rare-case-of-scleromalacia-perforans/