| Literature DB >> 31911771 |
Chaninan Kositkuljorn1, Poonkiat Suchonwanit1.
Abstract
Darier's disease is a relatively rare autosomal dominant genodermatosis with a defect in the desmosomal attachment due to a mutation in the ATP2A2 gene. The condition is characterized by multiple hyperkeratotic papules predominantly in seborrheic areas on the head, neck, and trunk, with less frequent involvement of the oral mucosa. Histopathologically, the lesions reveal suprabasal clefts in the epithelium with acantholytic and dyskeratotic cells. Facial involvement in Darier's disease is one of the common presenting features. However, it has been once reported in a severe, chronic form as leonine facies in a long-standing case. To raise awareness of facial involvement in Darier's disease, we herein report a 65-year-old female patient with prominent facial lesions.Entities:
Keywords: Corps ronds and grains; Darier-White disease; Dyskeratosis follicularis; Hyperkeratotic papule; Keratosis follicularis; Leonine facies
Year: 2019 PMID: 31911771 PMCID: PMC6940465 DOI: 10.1159/000504925
Source DB: PubMed Journal: Case Rep Dermatol ISSN: 1662-6567