Bigliardi Paul Lorenzo, Braschler Claudia, Kuhn Peter, Sigrist Johannes, Buechner Stanislaw, Rufli Theo
Department of Dermatology, Kantonsspital Schaffhausen, Switzerland.
Pediatr Dermatol. 2004 Jul-Aug;21(4):454-7. doi: 10.1111/j.0736-8046.2004.21406.x.
We present the case of a newborn male with aplasia cutis congenita on the extensor side of the right leg, with unilateral absence of skin on the lower limb. There was no abnormality in pregnancy or birth and there was no associated malformation or skin disease such as blistering or nail pathology. The management of this large ulcer was conservative, using silver sulfadiazine ointment, and healing occurred within 3 months. The follow-up after 21 months showed little scar formation and no handicap regarding function and appearance. The psychomotor development was normal. According to the classification outlined by Frieden, we classified this condition as type VII aplasia cutis congenita.
我们报告一例患有先天性皮肤发育不全的新生儿男性病例,其右腿伸侧出现先天性皮肤发育不全,下肢单侧皮肤缺失。妊娠及分娩过程均无异常,也无相关畸形或皮肤病,如水泡或指甲病变。对于这个大溃疡的处理采用保守治疗,使用磺胺嘧啶银软膏,3个月内愈合。21个月后的随访显示几乎没有瘢痕形成,在功能和外观方面均无缺陷。精神运动发育正常。根据Frieden概述的分类方法,我们将此病例归类为VII型先天性皮肤发育不全。