Postgraduate Program in Pathology, School of Medicine, Fluminense Federal University, Niterói, RJ, Brazil.
Am J Dermatopathol. 2021 May 1;43(5):368-372. doi: 10.1097/DAD.0000000000001847.
Lichen planus (LP) is a mucocutaneous immune-mediated disease of unknown etiology. It is more prevalent in women and usually occurs between the third and sixth decades of life. Oral lesions may or may not be associated with skin and genital lesions. Although the role of genetic factors is still undetermined, reports of LP in more than one family member are not uncommon. However, the occurrence of LP in monozygotic twins is rare. We report a rare case of 42-year-old female monozygotic twins presenting oral LP. This report is even rarer because one of the patients had cutaneous lesions of an unusual variant of LP (LP pigmentosus) and the other had an uncommon association with lichen sclerosus. The etiology and pathogenesis of LP are still uncertain. However, despite being rare, its occurrence in family members and monozygotic twins suggests that genetic factors are involved in its development.
扁平苔藓(LP)是一种病因不明的黏膜皮肤免疫介导性疾病。它在女性中更为常见,通常发生在第三和第六个十年。口腔病变可能与皮肤和生殖器病变有关,也可能没有。虽然遗传因素的作用仍不确定,但 LP 报告在一个以上家庭成员中并不罕见。然而,同卵双胞胎中 LP 的发生却很少见。我们报告了一例罕见的 42 岁女性同卵双胞胎口腔 LP 病例。这一报告更加罕见,因为其中一位患者有罕见的 LP 色素沉着变体(LP pigmentosus)的皮肤病变,另一位患者则伴有少见的硬化性苔藓的关联。LP 的病因和发病机制仍不清楚。然而,尽管它很少见,但它在家庭成员和同卵双胞胎中的发生表明遗传因素参与了其发病过程。