E-ISSN 2651-3455 (Online) | ISSN 2630-5593 (Print)
The Anatolian Journal of Family Medicine Linear lichen planus: two case reports [anatol j fm]
anatol j fm. 2019; 2(1): 41-44 | DOI: 10.5505/anatoljfm.2018.25633

Linear lichen planus: two case reports

Gülhan Gürel1, Sevinç Şahin2, Emine Çölgeçen1
1Department of Dermatology, Bozok University School of Medicine, Yozgat, Turkey
2Department of Pathology, Bozok University School of Medicine, Yozgat, Turkey

Lichen planus is an idiopathic inflammatory skin disease which affects the skin, mucosa, nails, and hairs of middle aged individuals. Linear lichen planus (LLP) is a rare variant of lichen planus characterized by pruritic, lichenoid appearance, violaceous-color papules in a linear pattern. About 0.24 to 0.62% of patients with lichen planus have been reported to have linear lichen planus. In cases with lichen planus, linear lesions can be post-traumatically seen as widespread generalized eruptions (Koebner phenomenon) and as zosteriforms on herpes infection as the Wolf’s isotopic response. However, LLP indicates the presence of spontaneous LLP lesions which follow Blaschko’s lines without any previous association with trauma or herpes infection. Herein, we present two cases with LLP and emphasize the rarity of these cases and the importance of linear lesions in the differential diagnosis.

Keywords: Lichen planus, linear, Blaschko

Gülhan Gürel, Sevinç Şahin, Emine Çölgeçen. Linear lichen planus: two case reports. anatol j fm. 2019; 2(1): 41-44

Corresponding Author: Gülhan Gürel, Türkiye
Manuscript Language: English
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