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中毒性表皮坏死松解症伴严重高胆红素血症:胆红素降低治疗后完全再上皮化。

Toxic epidermal necrolysis with severe hyperbilirubinemia: complete re-epithelialization after bilirubin reduction therapies.

机构信息

Department of Dermatology, Graduate School of Medicine, Chiba University, Chuo-ku, Chiba, Japan.

出版信息

J Dermatol. 2010 Jun;37(6):534-6. doi: 10.1111/j.1346-8138.2009.00770.x.

Abstract

Toxic epidermal necrolysis is a life-threatening skin disorder, and its mortality rate is estimated to be approximately 20-30%. It is characterized that more than 30% of the skin surface is eroded, however, skin lesions are usually re-epithelialized within 2-3 weeks. Previously, we reported a fatal case of toxic epidermal necrolysis with hyperbilirubinemia, and more than 60% of body surface areas had been eroded for 9 weeks. For the reason of delayed re-epithelialization, we hypothesized that hyperbilirubinemia was the culprit because bilirubin damaged cultured keratinocytes in vitro. In this case, we had an opportunity to treat another case of toxic epidermal necrolysis with severe hyperbilirubinemia. In order to reduce serum bilirubin levels, we performed bilirubin adsorption therapies, and skin lesions were successfully re-epithelialized within 4 weeks. Though further studies are required, we considered that bilirubin adsorption therapies are worth trying for toxic epidermal necrolysis with hyperbilirubinemia, especially for the cases suffering from delayed re-epithelialization.

摘要

中毒性表皮坏死松解症是一种危及生命的皮肤疾病,其死亡率估计约为 20-30%。其特征为超过 30%的皮肤表面被侵蚀,但皮肤损伤通常在 2-3 周内重新上皮化。此前,我们报告了一例致命性中毒性表皮坏死松解症合并高胆红素血症的病例,超过 60%的体表面积被侵蚀达 9 周。由于延迟再上皮化,我们假设高胆红素血症是罪魁祸首,因为胆红素在体外损伤培养的角质形成细胞。在该病例中,我们有机会治疗另一位患有严重高胆红素血症的中毒性表皮坏死松解症患者。为了降低血清胆红素水平,我们进行了胆红素吸附治疗,皮肤损伤在 4 周内成功再上皮化。尽管需要进一步研究,但我们认为胆红素吸附治疗对于高胆红素血症中毒性表皮坏死松解症,特别是对于那些有延迟再上皮化的病例,值得一试。

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