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先天性大疱性表皮松解症(简称 CEB)为少见的遗传性皮肤病,现报告一例。病史摘要患儿吴×,男,10天,于1984年9月13日住院。患儿系 G_3P_3,正常分娩,产后当天于大腿外侧出现一蚕豆大小水疱,以后水疱渐增多,及至第三天波及全身,第十天住院.其母共怀孕3胎,前2胎均为男性,正常分娩,生后一般情况可,但分别于生后第二、三天,全身出现大疱,与本患儿皮损雷同,未经治疗,均于生后月余死亡。父母非近亲联婚,父体健,否认母孕期服药史,亲属中无类似疾病史。
Congenital bullous epidermolysis (referred to as CEB) is a rare hereditary dermatosis, is now a report. Medical history Abstract Child Wu ×, male, 10 days, was hospitalized on September 13, 1984. Children with G_3P_3, normal childbirth, the day after giving birth in the thigh outside the size of a blister blisters, after the blisters increased, and the third day spread to the whole body, hospitalized on the tenth day of her mother a total of 3 pregnancies, the first two tires are men, Normal childbirth, after birth, the general situation can be, but respectively, in the second and third days after birth, the body appeared bullae, with the same children with lesions, untreated, were killed in more than a month after birth. Parents of non-relatives of marriage, father body health, denied mother’s medication history, no similar family history of disease.