Hpv-independent differentiated vulvar intraepithelial neoplasia (dvin) is associated with an aggressive clinical course
<p>Differentiated vulvar intrapeithelial neoplasia (dVIN) is an human papillomavirus (HPV)-independent precursor of squamous cell carcinoma (SCC), and the aim of this study was to better characterize its natural history. Cases of dVIN were identified from the pathology archives. Outcomes of pa...
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| Hauptverfasser: | , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
01 November 2017
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| In: |
International journal of gynecological pathology
Year: 2017, Jahrgang: 36, Heft: 6, Pages: 507-516 |
| ISSN: | 1538-7151 |
| DOI: | 10.1097/PGP.0000000000000375 |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1097/PGP.0000000000000375 Verlag, Volltext: https://insights.ovid.com/crossref?an=00004347-201711000-00001 
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| Verfasserangaben: | Jessica N. Mcalpine, So Youn Kim, Ardalan Akbari, Sima Eshragh, Miriam Reuschenbach, Magnus von Knebel Doeberitz, Elena S. Prigge, Suzanne Jordan, Naveena Singh, Dianne M. Miller, C. Blake Gilks |
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| 245 | 1 | 0 | |a Hpv-independent differentiated vulvar intraepithelial neoplasia (dvin) is associated with an aggressive clinical course |c Jessica N. Mcalpine, So Youn Kim, Ardalan Akbari, Sima Eshragh, Miriam Reuschenbach, Magnus von Knebel Doeberitz, Elena S. Prigge, Suzanne Jordan, Naveena Singh, Dianne M. Miller, C. Blake Gilks |
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| 520 | |a <p>Differentiated vulvar intrapeithelial neoplasia (dVIN) is an human papillomavirus (HPV)-independent precursor of squamous cell carcinoma (SCC), and the aim of this study was to better characterize its natural history. Cases of dVIN were identified from the pathology archives. Outcomes of patients with dVIN only, without associated invasive SCC, were compared with a cohort of patients with high-grade squamous intraepithelial lesion [HSIL(VIN3)]. Eighteen patients diagnosed with dVIN with adjacent invasive SCC (SCC/dVIN) and 7 patients with dVIN only, without invasive carcinoma, were identified. Mean age in both cohorts was 75 yr. All lesions but 1 were unifocal. In 35% of SCC/dVIN cases the surgical resection margins were positive for SCC, with 75% and 60% having margins positive for dVIN in the SCC/dVIN and dVIN-only cohorts, respectively. In total, 23/25 women with dVIN only or dVIN/SCC, for whom there was follow-up information, experienced either progression to or recurrence of invasive SCC, respectively, at a median of 1.1 yr, including all but 1 case of dVIN only, where the median time of progression to invasive SCC was 1.9 yr. A total of 22/25 women died of disease with a median overall survival of 3.4 yr. The outcome (i.e. progression to invasive carcinoma) of patients with dVIN only was significantly worse than that of a comparison group of 18 patients with HSIL(VIN3) (progression-free survival log-rank, P<0.001; disease-specific survival, P=0.04; overall survival, P=0.01). Six of 7 patients with dVIN only developed invasive carcinoma on follow-up, compared with 0 of 18 patients with HSIL(VIN3). The diagnosis of dVIN indicates the presence of a high-risk human papillomavirus-negative precursor of invasive SCC. These patients are likely to progress to invasive carcinoma over a relatively short period, at which point their prognosis is guarded.</p> | ||
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