Bowen disease (BD), or squamous cell carcinoma (SCC) in situ, represents a histologically defined but biologically heterogeneous group of intraepithelial neoplasms arising across different epithelial compartments. Human papillomavirus (HPV) plays a well-established causal role in anogenital squamous intraepithelial neoplasia, whereas its contribution to extragenital BD, including nail apparatus and general cutaneous lesions, has remained controversial. We performed a narrative review of the literature to synthesize current evidence on HPV prevalence, genotype distribution, and pathogenetic relevance in BD across three anatomical sites: nail apparatus, general cutaneous skin, and anogenital region. Available data reveal a clear site-dependent gradient of HPV involvement. Anogenital BD is overwhelmingly driven by high-risk α-HPV genotypes and shares molecular hallmarks of HPV-mediated carcinogenesis. Nail apparatus BD shows a consistently high prevalence of transforming α-HPV types, suggesting a biologically distinct subset of extragenital disease. In contrast, general cutaneous BD demonstrates highly variable HPV detection, predominantly involving β- and occasionally γ-HPV types, with evidence supporting a permissive or incidental rather than causal role. These findings indicate that BD should not be regarded as a unified viral neoplasm but as a convergent histologic phenotype arising from distinct pathogenetic pathways. Anatomical context is therefore essential for interpreting HPV detection and its diagnostic and clinical implications.

Dika, E., Baraldi, C., Venturi, F., Alessandrini, A.M., Vaccari, S., Venturoli, S., et al. (2026). Human Papillomavirus in Bowen Disease: Site-Specific Prevalence, Genotype Distribution, and Clinical Implications Across Nail Apparatus, Cutaneous, and Anogenital Sites. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 27(8), 1-14 [10.3390/ijms27083555].

Human Papillomavirus in Bowen Disease: Site-Specific Prevalence, Genotype Distribution, and Clinical Implications Across Nail Apparatus, Cutaneous, and Anogenital Sites

Dika E.;Baraldi C.;Venturi F.;Alessandrini A. M.;Vaccari S.;Venturoli S.;Argenziano G.;Ferrari T.;Lazzarotto T.;Magnaterra E.
2026

Abstract

Bowen disease (BD), or squamous cell carcinoma (SCC) in situ, represents a histologically defined but biologically heterogeneous group of intraepithelial neoplasms arising across different epithelial compartments. Human papillomavirus (HPV) plays a well-established causal role in anogenital squamous intraepithelial neoplasia, whereas its contribution to extragenital BD, including nail apparatus and general cutaneous lesions, has remained controversial. We performed a narrative review of the literature to synthesize current evidence on HPV prevalence, genotype distribution, and pathogenetic relevance in BD across three anatomical sites: nail apparatus, general cutaneous skin, and anogenital region. Available data reveal a clear site-dependent gradient of HPV involvement. Anogenital BD is overwhelmingly driven by high-risk α-HPV genotypes and shares molecular hallmarks of HPV-mediated carcinogenesis. Nail apparatus BD shows a consistently high prevalence of transforming α-HPV types, suggesting a biologically distinct subset of extragenital disease. In contrast, general cutaneous BD demonstrates highly variable HPV detection, predominantly involving β- and occasionally γ-HPV types, with evidence supporting a permissive or incidental rather than causal role. These findings indicate that BD should not be regarded as a unified viral neoplasm but as a convergent histologic phenotype arising from distinct pathogenetic pathways. Anatomical context is therefore essential for interpreting HPV detection and its diagnostic and clinical implications.
2026
Dika, E., Baraldi, C., Venturi, F., Alessandrini, A.M., Vaccari, S., Venturoli, S., et al. (2026). Human Papillomavirus in Bowen Disease: Site-Specific Prevalence, Genotype Distribution, and Clinical Implications Across Nail Apparatus, Cutaneous, and Anogenital Sites. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 27(8), 1-14 [10.3390/ijms27083555].
Dika, E.; Baraldi, C.; Venturi, F.; Alessandrini, A. M.; Vaccari, S.; Venturoli, S.; Argenziano, G.; Ferrari, T.; Lazzarotto, T.; Magnaterra, E....espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/1074591
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