2013
DOI: 10.1097/lgt.0b013e31826f2b2b
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Characterization of Squamous Cell Cancers of the Vulvar Anterior Fourchette by Human Papillomavirus, p16INK4a, and p53

Abstract: Different types of vulvar cancers can be found in squamous cell tumors of the anterior fourchette, similar to the finding in vulvar cancers from other locations and to what has previously been reported for vulvar squamous cell carcinomas in general.

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Cited by 31 publications
(20 citation statements)
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“…The variety in histopathologic features in dVIN is diverse ranging from atrophic to verruciform variants (10,12). Positive p53 staining might be helpful to differentiate between reactive changes and dVIN but not all cases of dVIN show p53 positivity in neoplastic cells which is in line with findings observed in VSCCs (24). The paradox that dVIN is less commonly diagnosed than HPV related VIN while most of the VSCCs are HPV negative has been ascribed to underdiagnoses of dVIN but it has also been hypothesized that the interval between HPV-negative dVIN and VSCC is much shorter than the interval between HPV-induced VIN and VSCC, The latter hypothesis is supported by the finding that women diagnosed with HPV-related VIN are much younger than women with dVIN (11).…”
Section: Cancer Epidemiol Biomarkers Prev; 25(8) August 2016supporting
confidence: 67%
“…The variety in histopathologic features in dVIN is diverse ranging from atrophic to verruciform variants (10,12). Positive p53 staining might be helpful to differentiate between reactive changes and dVIN but not all cases of dVIN show p53 positivity in neoplastic cells which is in line with findings observed in VSCCs (24). The paradox that dVIN is less commonly diagnosed than HPV related VIN while most of the VSCCs are HPV negative has been ascribed to underdiagnoses of dVIN but it has also been hypothesized that the interval between HPV-negative dVIN and VSCC is much shorter than the interval between HPV-induced VIN and VSCC, The latter hypothesis is supported by the finding that women diagnosed with HPV-related VIN are much younger than women with dVIN (11).…”
Section: Cancer Epidemiol Biomarkers Prev; 25(8) August 2016supporting
confidence: 67%
“…Positive HPV status was defined by concomitant positivity for high-risk HPV-DNA detection together with strong, diffuse p16 INK4a expression in both nucleus and cytoplasm of at least 70% of tumour cells, as this is considered to indicate truly HPV-transformed lesions (Klussmann et al , 2003a; Reuschenbach et al , 2013; Prigge et al , 2015, 2016). Briefly, DNA extracted from 10  μ m FFPE tissue sections using the DNeasy Blood and Tissue Kit (Qiagen, Hilden, Germany), corresponding to ∼10 × 10 mm tumour tissue, was analysed for HPV genotypes (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59, 68, 73 and 82) by PCR followed by bead-based hybridisation (Luminex Technology, Multimetrix, Progen, Heidelberg, Germany) (Schmitt et al , 2006; Prigge et al , 2015).…”
Section: Methodsmentioning
confidence: 99%
“…Unfortunately, Woelber et al and Nica et al studies had not speci ed the location of the tumors, if they were midline or lateral. 7,8,12 Over the past decade, there is an increasing trend for midline vulvar cancer [23][24][25][26] . This was con rmed with the majority cases in our recent study located at anterior fourchette.…”
Section: Discussionmentioning
confidence: 99%