Fischer M, Hamm H, Wirbelauer J
Universitäts-Kinderklinik Würzburg.
Klin Padiatr. 2004 Sep-Oct;216(5):288-93. doi: 10.1055/s-2004-44896.
Drug-related skin reactions often present as macular, maculopapular or urticarial rashes. Severe drug eruptions are rare, with life-threatening events occurring in about 4 per one million persons a year. In pediatric patients the estimated incidence of Stevens-Johnsons-syndrome (SJS) and toxic epidermal necrolysis (TEN) is even lower. They are often caused by antiepileptic drugs like carbamazepine.
A 10 (5)/ (12) year old boy of dark complexion suddenly developed a severe bullous skin disease six weeks after starting carbamazepine therapy due to focal epilepsy. Within few hours a life-threatening systemic inflammatory reaction occurred with subsequent respiratory failure. The clinical course was complicated by bacterial sepsis, bilateral thrombosis of the external iliacal veins and bilateral ocular symblephara. The skin healed with considerable pigmentary disturbance. We report the differential diagnostic and therapeutical features of toxic epidermal necrolysis and give a review of the literature.
药物相关的皮肤反应常表现为斑疹、斑丘疹或荨麻疹样皮疹。严重的药物疹较为罕见,每年每百万人口中约有4人发生危及生命的事件。在儿科患者中,史蒂文斯-约翰逊综合征(SJS)和中毒性表皮坏死松解症(TEN)的估计发病率甚至更低。它们常由卡马西平等抗癫痫药物引起。
一名10(5)/(12)岁肤色较深的男孩因局灶性癫痫开始服用卡马西平治疗六周后,突然患上严重的大疱性皮肤病。数小时内发生了危及生命的全身炎症反应,随后出现呼吸衰竭。临床过程因细菌性败血症、双侧髂外静脉血栓形成和双侧睑球粘连而复杂化。皮肤愈合后有明显的色素沉着紊乱。我们报告了中毒性表皮坏死松解症的鉴别诊断和治疗特点,并对文献进行了综述。