Seybold H, Simon M, Schuler G, Lüftl M
Dermatologische Klinik mit Poliklinik, Universitätsklinikum, Erlangen.
Hautarzt. 2006 Jan;57(1):47-50. doi: 10.1007/s00105-004-0889-y.
The clinical picture in vasculitis varies from few self-limiting symptoms to life-threatening illnesses affecting multiple organs. We describe the course of a woman patient who had had a severe cutaneous necrotizing vasculitis for more than 10 years. Various immunsuppressants, including cyclophosphamide, had failed to improve the clinical course, although adequate doses were given for a sufficient period. Treatment with DADPS (diaminodiphenylsulfone, dapsone), however, finally led to complete remission of the severe and chronic vasculitic ulcerations. Indications for DADPS treatment of inflammatory cutaneous diseases are discussed, and an overview of cutaneous vasculitis is provided.
血管炎的临床表现差异很大,从仅有少数自限性症状到危及生命的多器官疾病。我们描述了一名患有严重皮肤坏死性血管炎超过10年的女性患者的病程。尽管给予了足够剂量的多种免疫抑制剂,包括环磷酰胺,且用药时间足够长,但均未能改善临床病程。然而,使用二氨基二苯砜(DADPS,氨苯砜)治疗最终使严重的慢性血管炎性溃疡完全缓解。本文讨论了DADPS治疗炎性皮肤病的适应证,并提供了皮肤血管炎的概述。