AI Article Synopsis

  • In cervical biopsies, strong and diffuse p16 staining is crucial for diagnosing HPV-related conditions, while weak or focal p16 expression is considered nonspecific.
  • A study investigated high-risk HPV DNA presence in 20 biopsies with weak/focal p16 positivity, showing that 60% had hrHPV detected via CISH, highlighting diverse nuclear positivity patterns.
  • The findings suggest that patients with weak p16 expression, especially with high Ki67 levels, may need close monitoring and additional molecular tests for HPV detection.

Article Abstract

In cervical biopsies, for diagnosis of Human Papilloma Virus (HPV) related conditions, the immunohistochemical staining for p16 has a diagnostic value only if diffusely and strongly positive, pattern named "block-like". "Weak and/or focal (w/f) p16 expression" is commonly considered nonspecific. In our previous study, we demonstrated the presence of high-risk HPV (hrHPV) DNA by LiPa method in biopsies showing w/f p16 positivity. The aim of the present study was to investigate the presence of hrHPV-DNA by CISH in the areas showing w/f p16 expression. We assessed the presence of hrHPV16, 18, 31, 33, 51 by CISH in a group of 20 cervical biopsies showing w/f p16 expression, some with increased Ki67, and in 10 cases of block-like expression, employed as control. The immunohistochemical p16 expression was also assessed by digital pathology. hrHPV-CISH nuclear positivity was encountered in 12/20 cases of w/f p16 expression (60%). Different patterns of nuclear positivity were identified, classified as punctate, diffuse and mixed, with different epithelial distributions. Our results, albeit in a limited casuistry, show the presence of HPV in an integrated status highlighted by CISH in w/f p16 positive cases. This could suggest the necessity of a careful follow-up of the patients with "weak" and/or "focal" immunohistochemical patterns of p16, mainly in cases of increased Ki67 cell proliferation index, supplemented with molecular biology examinations.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11121605PMC
http://dx.doi.org/10.3390/ijms25105354DOI Listing

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