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Low detection rate of human papillomavirus in patients with cutaneous squamous cell carcinoma and keratoacanthoma

Authors
Baek, Yoo SangKim, Young ChanKim, Ko EunJeon, JiehyunKim, AereeSong, Hae JunKim, Chungyeul
Issue Date
Sep-2022
Publisher
John Libbey Eurotext
Keywords
human papillomavirus; keratinocyte carcinoma; keratoacanthoma; next-generation sequencing; squamous cell carcinoma
Citation
European Journal of Dermatology, v.32, no.5, pp 577 - 583
Pages
7
Indexed
SCIE
SCOPUS
Journal Title
European Journal of Dermatology
Volume
32
Number
5
Start Page
577
End Page
583
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/62967
DOI
10.1684/ejd.2022.4332
ISSN
1167-1122
1952-4013
Abstract
Background: The role of human papillomavirus (HPV) in keratoacanthoma (KA) remains unclear. Objectives: To identify possible differences in HPV DNA, detected by next-generation sequencing (NGS), between KAs and cutaneous squamous cell carcinomas (cSCCs), which may suggest different pathogenesis. Materials & Methods: We extracted DNA from formalin-fixed and paraffin-embedded (FFPE) tissue blocks from samples of 151 patients (105 with cSCCs and 46 with KAs). HPV DNA was detected using the NGS-based Ezplex® kit. HPV detection rates and other clinical characteristics were compared. Results: HPV was detected in 6.7% (7/105) of cSCC and 10.9% (5/46) of KA samples. Eight alpha-HPV genotypes (16, 57, 81, 31, 33, 45, 53, and 58) were detected, with HPV 16 being the most common. Only one type (57) is commonly classified as cutaneous type, and the rest are all mucosal types. HPV detection rate did not significantly differ between the KA and cSCC groups. Conclusion: HPV detection was relatively low in KA and cSCC samples. HPV might be related to the pathogenesis of only selected KA and cSCC cases. © 2022, JLE/Springer.
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2. Clinical Science > Department of Dermatology > 1. Journal Articles

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