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Darier’s Disease: A Case Report and Review of Literature Cover

Darier’s Disease: A Case Report and Review of Literature

By: L. Dourmishev and  A. Bitolska  
Open Access
|Feb 2026

Abstract

Introduction

Darier’s disease is an autosomal dominant disorder caused by mutations in the ATP2A2 gene, and clinically presented with hyperkeratotic papules and plaques in a seborrheic region.

Clinical Case Description

We observed a 48-year-old male patient who presented with persistent pruritic skin lesions on the trunk and extremities. Physical examination revealed erythematous and hyperkeratotic papules and follicular keratosis. The diagnosis of Darier’s disease was based on the clinical presentation and confirmed with histological examination. Treatment with low-dose methylprednisolone resulted in significant improvement.

Discussion and Conclusions

The case highlights the importance of considering Darier’s disease in patients with persistent pruritic skin lesions and emphasizes the need for accurate diagnosis and adequate treatment.

DOI: https://doi.org/10.2478/amb-2026-0013 | Journal eISSN: 2719-5384 | Journal ISSN: 0324-1750
Language: English
Page range: 84 - 87
Submitted on: May 7, 2025
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Accepted on: Jun 5, 2025
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Published on: Feb 21, 2026
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2026 L. Dourmishev, A. Bitolska, published by Medical University - Sofia
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.