Wu J J, Huang D B, Pang K R, Hsu S, Tyring S K
Department of Dermatology, University of California, Irvine, Irvine, CA, USA.
Br J Dermatol. 2005 Aug;153(2):254-73. doi: 10.1111/j.1365-2133.2005.06747.x.
Thalidomide was first introduced in the 1950s as a sedative but was quickly removed from the market after it was linked to cases of severe birth defects. However, it has since made a remarkable comeback for the U.S. Food and Drug Administration-approved use in the treatment of erythema nodosum leprosum. Further, it has shown its effectiveness in unresponsive dermatological conditions such as actinic prurigo, adult Langerhans cell histiocytosis, aphthous stomatitis, Behçet's syndrome, graft-versus-host disease, cutaneous sarcoidosis, erythema multiforme, Jessner-Kanof lymphocytic infiltration of the skin, Kaposi sarcoma, lichen planus, lupus erythematosus, melanoma, prurigo nodularis, pyoderma gangrenosum and uraemic pruritus. This article reviews the history, pharmacology, mechanism of action, clinical uses and adverse effects of thalidomide.
沙利度胺于20世纪50年代首次作为镇静剂推出,但在与严重出生缺陷病例相关联后很快就从市场上撤下。然而,此后它在美国食品药品监督管理局批准用于治疗麻风结节性红斑后显著卷土重来。此外,它在一些难治性皮肤病中也显示出有效性,如光化性瘙痒症、成人朗格汉斯细胞组织细胞增多症、阿弗他口炎、白塞病、移植物抗宿主病、皮肤结节病、多形红斑、耶斯纳 - 卡诺夫皮肤淋巴细胞浸润症、卡波西肉瘤、扁平苔藓、红斑狼疮、黑色素瘤、结节性瘙痒症、坏疽性脓皮病和尿毒症瘙痒症。本文综述了沙利度胺的历史、药理学、作用机制、临床用途和不良反应。