Amin Sima, Fiore Connie T, Paek So Yeon
Texas A&M College of Medicine, College StationTexas.
Division of Dermatology, Baylor University Medical CenterDallasTexas.
Proc (Bayl Univ Med Cent). 2019 Jan 14;32(1):90-92. doi: 10.1080/08998280.2018.1528962. eCollection 2019 Jan.
Bullous pemphigoid (BP) is a blistering dermatosis characterized by an autoimmune response to two hemidesmosomal proteins, BP180 and BP230. We describe a case of an 80-year-old man diagnosed with BP by clinical features, histopathology, and immunosorbent assay who developed milia within resolving BP lesions. Milia formation during recovery is common in cases of mucous membrane pemphigoid and epidermolysis bullosa acquisita but has rarely been reported in cases of BP.
大疱性类天疱疮（BP）是一种水疱性皮肤病，其特征是对两种半桥粒蛋白BP180和BP230产生自身免疫反应。我们描述了一例80岁男性患者，通过临床特征、组织病理学和免疫吸附试验诊断为BP，在BP皮损消退过程中出现了粟丘疹。在黏膜类天疱疮和获得性大疱性表皮松解症病例中，恢复过程中形成粟丘疹很常见，但在BP病例中鲜有报道。
