Syring F M, Zillikens D, Schmidt E, Kasperkiewicz M
Klinik für Dermatologie, Allergologie und Venerologie, Universität Lübeck, Ratzeburger Allee 160, 23538, Lübeck, Deutschland.
Hautarzt. 2019 May;70(5):367-370. doi: 10.1007/s00105-019-4402-z.
A 53-year-old man presented with a 37-year history of erosive and scarring mucosal lesions of several organs. An initial diagnosis of Stevens-Johnson syndrome was maintained for many years. Due to late correct diagnosis of an anti-laminin 332 mucous membrane pemphigoid and the fact that early, targeted, intensified immunosuppressive therapy was not initiated, the disease led to almost complete loss of vision and obstruction of airways.
一名53岁男性,有多个器官糜烂性和瘢痕性黏膜病变37年病史。最初诊断为史蒂文斯-约翰逊综合征并维持多年。由于抗层粘连蛋白332黏膜类天疱疮诊断延误,且未早期启动针对性强化免疫抑制治疗,该病导致几乎完全失明和气道梗阻。