斯蒂文斯-约翰综合症（Stevens - John syndrome）.doc

斯蒂文斯-约翰综合症（Stevens - John syndrome） Stevens Johnson syndrome Ask for the edit encyclopedia card In 1922, Stevens and Johnson described the "stevenson-johnson syndrome" in detail. The syndrome is a kind of involvement of the skin and mucous membrane of the diseased acute blister Stevens Johnson syndrome can occur in some infection or oral drugs after the mild erythema multiforme is a skin blister lesions, erythema multiforme further development of the formation of toxic epidermal necrolysis, this is a kind of acute fatal disease. The condition of the disease is severe in the eyes, and the lesions may be involved in the cornea, the conjunctiva, the conjunctiva and the eyelids. directory epidemiology The cause of The pathogenesis of Clinical manifestations of Diagnosis & treatment diagnosis check treatment Prognostic epidemiology The cause of The pathogenesis of Clinical manifestations of Diagnosis & treatment diagnosis check treatment The prognosis Expand the epidemiology of this section 1. The incidence of the morbidity of stevenson-johnson syndrome is lower. Char et al reports that only 4.2 out of every 1 million people have a stevenson-johnson syndrome every year. Schoph et al. Reported that the incidence of stevenson-johnson syndrome in Germany was 1.1/1 million per year. The incidence rate reported in France is 1.2/1 million to 1.3 million per year, while the incidence rate in Italy is 0.6/1 million. There have been no reports of the incidence of stevenson-johnson syndrome in China. 2. In the incidence of ocular complications, 80% of patients with stevenson-johnson syndrome have ocular complications in some serious cases, and acute complications include keratitis and corneal perforation. Chronic complications include conjunctival scarring, dry eye and blepharospheric adhesions. These complications can be secondary to corneal damage, leading to the occurrence of long-term complications of about a third of the people with stevenson-johnson syndrome with significant