Odeshi Oluwatosin, Kenny Bret, Kogilwaimath Siddharth, Oroz Irina, Osmond Allison
Department of Dermatology, Saskatchewan Health Authority, Saskatoon, SK, Canada.
Faculty of Medicine, Memorial University, St. John's, NL, Canada.
SAGE Open Med Case Rep. 2022 Apr 14;10:2050313X221086322. doi: 10.1177/2050313X221086322. eCollection 2022.
Lichenoid granulomatous dermatitis, also known as giant cell lichenoid dermatitis, represents an uncommon mixed-pattern dermatitis with histopathologic features of interface dermatitis with band-like lymphocytic inflammation of the dermal-epidermal junction, with thinning of the epidermis or lichen planus-like changes, and granulomatous inflammation involving the dermis. Lichenoid granulomatous dermatitis can manifest with a variety of primary lesions and has various clinical associations. We present a challenging clinicopathologic case of lichenoid granulomatous dermatitis in a 58-year-old woman with dramatic cutaneous desquamation in the context of a complex medical history and multiple potential triggers.
苔藓样肉芽肿性皮炎,也称为巨细胞苔藓样皮炎,是一种罕见的混合型皮炎,具有界面性皮炎的组织病理学特征,表现为真皮 - 表皮交界处带状淋巴细胞炎症,伴有表皮变薄或扁平苔藓样改变,以及累及真皮的肉芽肿性炎症。苔藓样肉芽肿性皮炎可表现为多种原发性皮损,并具有多种临床关联。我们报告了一例具有挑战性的苔藓样肉芽肿性皮炎临床病理病例,患者为一名58岁女性,在复杂的病史和多种潜在诱因背景下出现严重的皮肤脱屑。