Lugović-Mihić Liborija, Duvančić Tomislav, Pavić Ivana, Gverić-Grginić Ana, Šitum Mirna, Dediol Iva
Professor Liborija Lugović Mihić, MD, PhD, Department of Dermatovenereology, Sestre milosrdnice University Hospital Center, Vinogradska cesta 29, 10 000 Zagreb, Croatia;
Acta Dermatovenerol Croat. 2019 Sep;27(3):184-187.
Bullous pemphigoid (BP) is an autoimmune disorder which is usually chronic, with blistering that predominantly affects the skin and occasionally the mucosa, and which includes several different types. One of them is a very rare dyshidrosiform type which is localized on the hands and feet with small or large blisters on the palmoplantar surfaces. BP resulting from a drug reaction is a relatively rare occurrence, and so far more than 50 different medications have been identified as triggers. The aim of this article was to present the case of a paraplegic patient who developed this rare dyshidrosiform type of BP while he was being neurologically treated with baclofen. In spite of therapy with systemic and topical corticosteroids and other measures, successful treatment was achieved only after eliminating baclofen from the patient's regimen. His general state of health was seriously endangered due to nasal and skin methicillin-resistant Staphylococcus aureus (MRSA), urinary infection, and oral mycosis (soor), and he was at high risk of sepsis and a fatal outcome. Through our efforts, however, we managed to achieve an excellent outcome. According to our knowledge, this was the first case of baclofen-induced dyshidrosiform BP.
大疱性类天疱疮(BP)是一种自身免疫性疾病,通常为慢性,水疱主要累及皮肤,偶尔累及黏膜,包括几种不同类型。其中一种是非常罕见的汗疱疹样型,局限于手足,掌跖面有大小不等的水疱。药物反应引起的BP相对少见,迄今为止已确定50多种不同药物可引发该病。本文旨在介绍一名截瘫患者的病例,该患者在接受巴氯芬神经治疗期间发生了这种罕见的汗疱疹样型BP。尽管采用了全身和局部皮质类固醇治疗及其他措施,但仅在从患者治疗方案中停用巴氯芬后才成功治愈。由于鼻腔和皮肤耐甲氧西林金黄色葡萄球菌(MRSA)感染、泌尿系统感染和口腔真菌病(鹅口疮),他的总体健康状况受到严重威胁,并有败血症和致命结局的高风险。然而,通过我们的努力,我们成功取得了良好的结果。据我们所知,这是首例巴氯芬诱发的汗疱疹样BP病例。