Faculty of Health and Medicine, University of Newcastle, Callaghan, New South Wales, Australia.
John Hunter Hospital, Maternity and Gynecology, New Lambton Heights, New South Wales, Australia.
J Low Genit Tract Dis. 2018 Oct;22(4):387-395. doi: 10.1097/LGT.0000000000000419.
Three types of lichen planus (LP) occur on the vulva: erosive, classic, and hypertrophic. The latter 2 occur on keratinized skin and little is known about their clinicopathologic appearance.
Vulvar biopsies of keratinized skin reported as LP or "lichenoid" between 2011 and 2017 were reviewed. Inclusion required age of older than 18 years, a lichenoid tissue reaction, and insufficient abnormal dermal collagen to diagnose lichen sclerosus. Clinical and histopathologic data were collected and cases were categorized as hypertrophic, classic, or nonspecific lichenoid dermatosis. Descriptive statistics were performed and groups were compared with the Fisher exact test.
Sixty-three cases met criteria for inclusion. Twenty-nine (46%) cases were categorized as hypertrophic LP, 21 (33%) as classic LP, and 13 (21%) as nonspecific lichenoid dermatosis. There were no significant differences in age, primary symptom, biopsy location, or duration of disease between the 3 groups. When compared with classic and nonspecific disease, hypertrophic LP was less likely to have comorbid dermatoses and more likely to be red, diffuse, have scale crust, and contain plasma cells in the infiltrate. Nonspecific disease had similar clinical features to classic LP but was less likely than the other 2 categories to have a dense lymphocytic infiltrate and exocytosis.
Vulvar LP on keratinized skin has a diversity of appearances and presents a clinicopathologic challenge. Further research is required to understand the natural history of hypertrophic LP and the underlying diagnosis of nonspecific lichenoid cases.
外阴部有三种扁平苔藓(LP):糜烂型、经典型和肥厚型。后两种发生在角化皮肤,对其临床病理表现知之甚少。
回顾了 2011 年至 2017 年间报告为 LP 或“苔藓样”的角化皮肤外阴活检。纳入标准为年龄大于 18 岁,有苔藓样组织反应,且真皮胶原异常不足不足以诊断硬化性苔藓。收集了临床和组织病理学数据,并将病例分为肥厚型、经典型或非特异性苔藓样皮肤病。进行了描述性统计,并用 Fisher 精确检验比较组间差异。
符合纳入标准的有 63 例。29 例(46%)归类为肥厚型 LP,21 例(33%)为经典型 LP,13 例(21%)为非特异性苔藓样皮肤病。三组间在年龄、主要症状、活检部位和疾病持续时间方面无显著差异。与经典和非特异性疾病相比,肥厚型 LP 更不可能伴有其他皮肤病,且更可能为红色、弥漫性、有鳞屑和痂皮,浸润中含有浆细胞。非特异性疾病的临床特征与经典 LP 相似,但与其他两种类型相比,其淋巴细胞浸润和细胞外溢更不密集。
角化皮肤的外阴 LP 具有多种表现,给临床病理带来挑战。需要进一步研究以了解肥厚型 LP 的自然病程和非特异性苔藓样病例的潜在诊断。