JOURNAL ARTICLE

Dermatopathology.

  • Published In: Clinical & Experimental Dermatology, 2025, v. 50, n. 5. P. 1053 1 of 3

  • Database: Academic Search Ultimate 2 of 3

  • Authored By: Teng, Yi-Shan; Sun, Yng 3 of 3

Abstract

The article focuses on a case study of a 30-year-old woman diagnosed with spiny keratoderma, a rare skin condition characterized by rough, keratotic papules on the palms and soles. Despite various treatments, her symptoms persisted, prompting a skin biopsy that confirmed the diagnosis through histopathological analysis. Spiny keratoderma can be either acquired or inherited, with potential links to malignancies in acquired cases. The article discusses differential diagnoses, including arsenical keratosis and multiple filiform warts, emphasizing the importance of accurate diagnosis due to associated health risks. Treatment options for spiny keratoderma are limited and may include topical therapies and dermabrasion. [Extracted from the article]

Additional Information

  • Source:Clinical & Experimental Dermatology. 2025/05, Vol. 50, Issue 5, p1053
  • Document Type:Article
  • Subject Area:Science
  • Publication Date:2025
  • ISSN:0307-6938
  • DOI:10.1093/ced/llae518
  • Accession Number:185321494
  • Copyright Statement:Copyright of Clinical & Experimental Dermatology is the property of Oxford University Press / USA and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

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