Publication: Sporadic Progressive Symmetric Erythrokeratoderma: Classical Presentation of a rare Condition
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Date
2019
Article Type
Case Report
Journal Title
Journal ISSN
ISSN 2091-0231 eISSN 2091-167X
Volume Title
Pages
Pages: 69 - 72
Publisher
Society of Dermatologists, Venereologists and Leprologists of Nepal (SODVELON)
Abstract
Abstract:
Progressive symmetrical erythrokeratodermia (PSEK) is a rare autosomal dominant genodermatosis presenting in infancy or early childhood. An 11-year-old male presented with a history of pruritic, erythematous, scaly, hyperkeratotic plaques first noted at 5 years of age, with no history of similar lesions in the family. Cutaneous examination revealed multiple, irregularly shaped, erythematous plaques with fine, shiny white, adherent scaling distributed symmetrically over the face, trunk, inguinal area, bilateral axillae and extensor surfaces of limbs. Palmoplantar keratoderma was present with thickened, yellowish discolored nails. No systemic abnormality was found. The histopathological findings were consistent with PSEK. The case is being reported to increase the awareness about this rare disease.
Keywords: Genetic Heterogeneity, Keratoderma, palmoplantar, Nepal, Retinoids
Description
Kompal Agarwal
BP Koirala Institute of Health Sciences
Sudha Agrawal
BP Koirala Institute of Health Sciences, Dharan
Anju Pradhan
BP Koirala Institute of Health Sciences, Dharan
Keywords
Identifier
https://doi.org/10.3126/njdvl.v17i1.23293