Kohut Ihor, Kalmykova Antonina, Bezkorovayna Halyna
Dermatology, Skin Health Center, Ternopil, UKR.
Dermatopathology, Pathology Laboratory (Experimental Pathology Laboratories), Kyiv, UKR.
Cureus. 2025 May 10;17(5):e83828. doi: 10.7759/cureus.83828. eCollection 2025 May.
Brunsting-Perry pemphigoid is a rare, chronically persistent bullous dermatosis, localized to the head, scalp, and neck, causing residual scars and cicatricial alopecia. Herein, we present a case of Brunsting-Perry pemphigoid in a 68-year-old Caucasian woman presenting with over 10 years of history of slowly progressing patchy cicatricial alopecia. Dermoscopy showed scarring, a milky red background, and a typical picture of a "fried-egg sign" representing specific follicular damage. A skin biopsy revealed a subepidermal blister with dermal inflammation. Immunopathology shows strong linear continuous deposits of C3c and IgM along the basement membrane, and moderate to weak linear reactions to IgG and IgA. Intralesional betamethasone was successful in the treatment, and topical mometasone furoate lotion was used to maintain the result. Our case suggests that Brunsting-Perry pemphigoid may be underdiagnosed as the reason for scarring alopecia, considering the scarce information about the disease in the literature.
布伦斯汀-佩里类天疱疮是一种罕见的、慢性持续性大疱性皮肤病,局限于头部、头皮和颈部,可导致残留瘢痕和瘢痕性脱发。在此,我们报告一例68岁白种女性布伦斯汀-佩里类天疱疮病例,该患者有超过10年缓慢进展的斑片状瘢痕性脱发病史。皮肤镜检查显示有瘢痕形成、乳红色背景以及代表特定毛囊损伤的典型“煎蛋征”表现。皮肤活检显示表皮下水疱伴真皮炎症。免疫病理学检查显示C3c和IgM沿基底膜呈强线性连续沉积,对IgG和IgA呈中度至弱线性反应。皮损内注射倍他米松治疗成功,外用糠酸莫米松洗剂维持治疗效果。我们的病例提示,鉴于文献中关于该疾病的信息较少,布伦斯汀-佩里类天疱疮可能因瘢痕性脱发而被漏诊。