Toxic epidermal necrolysis (TEN) and Stevens-Johnson syndrome (SJS) are severe, rare skin reactions, usually to drugs, and are associated with widespread destruction of the epidermis. The 2 diseases are closely related: SJS is a limited form characterized by mucous membrane erosions and blisters on limited areas of the skin (<10% of the total body surface area), and TEN resembles superficial burns because of the confluence of blisters and erosions on more than 30% of the total body surface area. Overlapping cases are defined by an intermediate extent of the skin lesions.
1 The incidence of SJS and TEN is approximately 2 cases per million persons per year,
2 and the overall mortality rate is 20% to 25%.
3 Ocular complications in SJS and TEN may occur acutely along with or after the onset of skin involvement. Severe ocular complications may even result in permanent visual loss due to corneal scarring or vascularization.
4-6 Little is currently known about the ocular symptoms of these diseases, particularly the long-term manifestations. Stevens-Johnson syndrome and TEN are viewed as a spectrum of systemic disease with increasing severity and mortality. A scoring system estimates severity and predicts mortality in patients with SJS or TEN.
7 However, it remains unclear whether there are factors predictive of the frequency and severity of ocular complications, both acutely and over the long term. This study aimed to describe acute and late ocular manifestations and complications in SJS and TEN and to identify possible clinical predictors for the development of ocular complications.