Evidence map›Paper›PMID 42773184›Full record

ReviewDermatologie (Heidelberg, Germany)2026

[Vulvar intraepithelial neoplasia and vulvar cancer].

M Hampl, Linn Wölber

Abstract readEnglish AbstractReview
PubMed Publisher
In one paragraph

Review in Dermatologie (Heidelberg, Germany), 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

2 authors.

M HamplFrauenklinik, Dysplasiezentrum, St. Elisabeth Krankenhaus Köln Hohenlind, Werthmannstr. 1, 50935, Köln, Deutschland. Monika.Hampl@hohenlind.de.
Linn WölberDysplasiezentrum Hamburg am Krankenhaus Jerusalem und Klinik für Gynäkologie, Universitätsklinikum Hamburg-Eppendorf, Martinistr. 52, 20246, Hamburg, Deutschland. lwoelber@uke.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vulvar intraepithelial neoplasia (VIN) is divided into human papillomavirus (HPV)-associated lesions (undifferentiated VIN, high-grade squamous intraepithelial lesion) and HPV-independent VIN (predominantly differentiated VIN). This new WHO classification is essential for the diagnostics, treatment and prognosis. While 90% of cases seen in practice are high-grade intraepithelial lesions (HSIL), dVIN cases are less common (10%), more difficult to diagnose and carry a higher risk of progression to cancer. The lichen sclerosus that most often underlies these lesions is responsible for these characteristics. The distinction between the two lesions is made using p53 and p16 immunohistochemistry on biopsy/excision specimens. Analogous to VIN, invasive carcinomas are also divided into HPV-associated and HPV-independent tumors. Here too, HPV-independent changes are associated with a worse prognosis. The treatment of dVIN is surgical, while treatment of uVIN can be ablative, surgical or medicinal (imiquimod being preferred). The recurrence rate is high regardless of the treatment chosen. Lifelong follow-up is therefore essential. In the case of an invasive carcinoma the majority of patients can be curatively treated with surgery alone. In cases of lymphatic metastasis, adjuvant chemo(radio)therapy is generally administered; in very advanced disease, particularly when continence function is threatened, primary chemoradiotherapy can also be used. Primary prevention of HPV-induced lesions is highly effective through primary HPV vaccination. Secondary prevention of dVIN/HPV-independent invasive carcinoma appears to be achievable through consistent maintenance therapy of the underlying lichen sclerosus with highly potent topical corticosteroids.

Indexed as

Carcinoma in SituPapillomavirus InfectionsVulvar NeoplasmsDiagnosis, DifferentialFemaleHuman Papillomavirus VirusesHumansPrognosisdVINHPV infectionImmunohistochemistryuVIN

Identifiers

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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.