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大疱性类天疱疮,其皮疹仅在寻常型白癜风的原有皮疹上发生。

Bullous Pemphigoid in Which Eruption Developed Exclusively on Preexisting Eruption of Vitiligo Vulgaris.

作者信息

Oka Masahiro, Fukumoto Takeshi

机构信息

Department of Dermatology, Kita-Harima Medical Center, Ono City, Japan.

Division of Dermatology, Department of Internal Related, Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

Case Rep Dermatol. 2020 Feb 4;12(1):33-36. doi: 10.1159/000505829. eCollection 2020 Jan-Apr.

Abstract

Coexistence of bullous pemphigoid (BP) and vitiligo vulgaris (VV) is very rare. We present a unique case of BP associated with VV in a 76-year-old Japanese man, in which BP eruption developed exclusively on preexisting VV regions. The patient was referred to us with a 3-month history of blistering eruption with severe pruritis on the right forearm and left lower limb. In addition, he had been suffering from a widespread depigmented eruption on the trunk and extremities for at least 20 years. Curiously, the blistering eruption developed exclusively on preexisting depigmented eruption. Histopathological and laboratory examinations identified the blistering eruption as BP. The depigmented eruption was diagnosed as VV. BP eruption responded quickly to oral prednisolone therapy, improving within 1 week, and the prednisolone dose was gradually tapered. Within 1 month, BP lesions almost completely resolved. In the present case, BP not only coexisted with VV, but also developed exclusively on preexisting vitiliginous regions. The present case strongly suggests that BP and VV are partly caused by common pathological mechanisms.

摘要

大疱性类天疱疮(BP)与寻常型白癜风(VV)并存极为罕见。我们报告了一例76岁日本男性患者,其BP与VV并存,且BP皮疹仅在已有的VV区域出现。该患者因右前臂和左下肢出现水疱性皮疹伴严重瘙痒3个月前来就诊。此外,他躯干和四肢广泛的色素脱失性皮疹至少已有20年。奇怪的是,水疱性皮疹仅在已有的色素脱失性皮疹部位出现。组织病理学和实验室检查确诊水疱性皮疹为BP,色素脱失性皮疹为VV。BP皮疹对口服泼尼松龙治疗反应迅速,1周内病情改善,泼尼松龙剂量逐渐减量。1个月内,BP皮损几乎完全消退。在本病例中,BP不仅与VV并存,还仅在已有的白癜风区域出现。本病例有力地提示BP和VV部分由共同的病理机制引起。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c594/7036583/26f7d10309cc/cde-0012-0033-g01.jpg

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