Evidence map›Paper›PMID 41047841›Full record

ReviewJournal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG2026

HPV42 - a human papillomavirus classified as a low-risk type with oncogenic potential.

Sven Niklas Burmann, Ulrike Wieland, Steffi Silling, Frank Oellig, David Chromy, Julia Hyun, Thilo Gambichler, Alexander Kreuter

Abstract readCase ReportsReview
In one paragraph

Review in Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Sven Niklas BurmannDepartment of Dermatology, Venereology and Allergology, Helios St. Elisabeth Hospital Oberhausen, University Witten/Herdecke, Oberhausen, Germany.
Ulrike WielandInstitute of Virology, National Reference Center for Papilloma- and Polyomaviruses, University of Cologne, Medical Faculty and University Hospital Cologne, Cologne, Germany.
Steffi SillingInstitute of Virology, National Reference Center for Papilloma- and Polyomaviruses, University of Cologne, Medical Faculty and University Hospital Cologne, Cologne, Germany.
Frank OelligInstitute of Pathology, Mülheim an der Ruhr, Germany.
David ChromyUniversity Department of Dermatology, Medical University of Vienna, Vienna, Austria.ORCID https://orcid.org/0000-0002-1807-8258
Julia HyunDepartment of Dermatology, Venereology and Allergology, Helios St. Johannes Klinik Duisburg, Duisburg, Germany.
Thilo GambichlerDepartment of Dermatology, Christian Hospital Unna, Unna, Germany.
Alexander KreuterDepartment of Dermatology, Venereology and Allergology, Helios St. Elisabeth Hospital Oberhausen, University Witten/Herdecke, Oberhausen, Germany.ORCID https://orcid.org/0000-0003-2275-499X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human papillomavirus (HPV) type 42 is a rare HPV type currently classified as "low-risk" and belongs to the alpha genus. It has primarily been detected in benign vulvar papillomas and is predominantly associated with benign lesions such as anogenital warts. However, in very rare cases, HPV42 has also been identified in invasive genital tumors, particularly cervical carcinomas. In the case series presented here, HPV42 was detected in anogenital warts, a digital squamous cell carcinoma in situ, and a lymphogenously metastasized digital papillary adenocarcinoma (DPA). In the latter tumor entity, HPV42 was recently identified as the potential causative agent. Depending on the infected cell population, HPV42 can give rise to both benign lesions (anogenital warts and the rare cervicovaginal "seborrheic keratosis-like" lesion) and malignant lesions (anogenital and digital carcinomas, as well as the highly aggressive DPA). HPV42 can therefore be considered as potentially carcinogenic. With the currently available nonavalent HPV vaccine over 90% of HPV-related tumors and anogenital warts can be prevented, but not HPV42-induced lesions. These tumors will therefore not be suppressed by the current vaccination programs, even not in countries with high vaccination rates.

Indexed as

Adenocarcinoma, PapillaryHuman Papillomavirus VirusesPapillomaviridaePapillomavirus InfectionsSkin NeoplasmsAdultAgedCarcinoma, Squamous CellCondylomata AcuminataHumansMaleMiddle AgedAnogenital wartscondylomata acuminatadigital papillary adenocarcinomaHPV42human papillomavirussquamous cell carcinoma

Identifiers

PMID41047841
PMCPMC13636108

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.