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The role of multiple high-risk human papillomavirus infections for cervical biopsies and findings in colposcopic procedures

OBJECTIVE: The clinical outcome of high-risk HPV (hr-HPV) infection varies according to genotype(s). Patients may harbor either one single hr-HPV (s-HPV) or multiple HPV (m-HPV) genotypes. Recently, the relationship between m-HPV infections and high-grade dysplasia has been investigated, and controv...

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Autores principales: Akış, Serkan, Öztürk, Uğur Kemal, Keleş, Esra, Alınca, Cihat Murat, Kabaca, Canan, Api, Murat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10258572/
https://www.ncbi.nlm.nih.gov/pubmed/36992075
http://dx.doi.org/10.4274/jtgga.galenos.2023.2022-8-10
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author Akış, Serkan
Öztürk, Uğur Kemal
Keleş, Esra
Alınca, Cihat Murat
Kabaca, Canan
Api, Murat
author_facet Akış, Serkan
Öztürk, Uğur Kemal
Keleş, Esra
Alınca, Cihat Murat
Kabaca, Canan
Api, Murat
author_sort Akış, Serkan
collection PubMed
description OBJECTIVE: The clinical outcome of high-risk HPV (hr-HPV) infection varies according to genotype(s). Patients may harbor either one single hr-HPV (s-HPV) or multiple HPV (m-HPV) genotypes. Recently, the relationship between m-HPV infections and high-grade dysplasia has been investigated, and controversial results have been obtained. Therefore, the clinical significance of m-HPV is not clear. This study aimed to evaluate which group is associated with higher grade dysplasia by analyzing colposcopic punch biopsies. MATERIAL AND METHODS: A total of 690 patients who were scheduled for a diagnostic excisional procedure between April 2016 and January 2019 due to the detection of high-grade cervical intraepithelial neoplasia (CIN 2/3) in colposcopy were included. Patients who were not scheduled for colposcopic examination or cervical punch biopsy, or who were scheduled for an excisional procedure due to smear-biopsy incompatibility or persistent low-grade dysplasia were excluded. Patients with a negative HPV test and an unknown HPV genotype were also excluded. RESULTS: Among the patients scheduled for excision (n=404), 74.5% had a s-HPV and 25.5% had a m-HPV infection. The proportion of CIN 1, 2 and 3 per patient in the m-HPV group was significantly higher than the s-HPV group (p=0.017). When this analysis was made for the number of CIN 2+3 per patient in the s-HPV and m-HPV groups, it was 1.29 (389/301) and 1.36 (140/103), respectively, and no difference was found (p=0.491). CONCLUSION: Patients in the m-HPV group, who underwent more colposcopic cervical biopsies, had higher numbers of CIN lesions, regardless of age and cytology results.
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spelling pubmed-102585722023-06-13 The role of multiple high-risk human papillomavirus infections for cervical biopsies and findings in colposcopic procedures Akış, Serkan Öztürk, Uğur Kemal Keleş, Esra Alınca, Cihat Murat Kabaca, Canan Api, Murat J Turk Ger Gynecol Assoc Original Investigation OBJECTIVE: The clinical outcome of high-risk HPV (hr-HPV) infection varies according to genotype(s). Patients may harbor either one single hr-HPV (s-HPV) or multiple HPV (m-HPV) genotypes. Recently, the relationship between m-HPV infections and high-grade dysplasia has been investigated, and controversial results have been obtained. Therefore, the clinical significance of m-HPV is not clear. This study aimed to evaluate which group is associated with higher grade dysplasia by analyzing colposcopic punch biopsies. MATERIAL AND METHODS: A total of 690 patients who were scheduled for a diagnostic excisional procedure between April 2016 and January 2019 due to the detection of high-grade cervical intraepithelial neoplasia (CIN 2/3) in colposcopy were included. Patients who were not scheduled for colposcopic examination or cervical punch biopsy, or who were scheduled for an excisional procedure due to smear-biopsy incompatibility or persistent low-grade dysplasia were excluded. Patients with a negative HPV test and an unknown HPV genotype were also excluded. RESULTS: Among the patients scheduled for excision (n=404), 74.5% had a s-HPV and 25.5% had a m-HPV infection. The proportion of CIN 1, 2 and 3 per patient in the m-HPV group was significantly higher than the s-HPV group (p=0.017). When this analysis was made for the number of CIN 2+3 per patient in the s-HPV and m-HPV groups, it was 1.29 (389/301) and 1.36 (140/103), respectively, and no difference was found (p=0.491). CONCLUSION: Patients in the m-HPV group, who underwent more colposcopic cervical biopsies, had higher numbers of CIN lesions, regardless of age and cytology results. Galenos Publishing 2023-06 2023-06-07 /pmc/articles/PMC10258572/ /pubmed/36992075 http://dx.doi.org/10.4274/jtgga.galenos.2023.2022-8-10 Text en © Copyright 2023 by the Turkish-German Gynecological Education and Research Foundation https://creativecommons.org/licenses/by-nc-nd/4.0/Journal of the Turkish-German Gynecological Association published by Galenos Publishing House.
spellingShingle Original Investigation
Akış, Serkan
Öztürk, Uğur Kemal
Keleş, Esra
Alınca, Cihat Murat
Kabaca, Canan
Api, Murat
The role of multiple high-risk human papillomavirus infections for cervical biopsies and findings in colposcopic procedures
title The role of multiple high-risk human papillomavirus infections for cervical biopsies and findings in colposcopic procedures
title_full The role of multiple high-risk human papillomavirus infections for cervical biopsies and findings in colposcopic procedures
title_fullStr The role of multiple high-risk human papillomavirus infections for cervical biopsies and findings in colposcopic procedures
title_full_unstemmed The role of multiple high-risk human papillomavirus infections for cervical biopsies and findings in colposcopic procedures
title_short The role of multiple high-risk human papillomavirus infections for cervical biopsies and findings in colposcopic procedures
title_sort role of multiple high-risk human papillomavirus infections for cervical biopsies and findings in colposcopic procedures
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10258572/
https://www.ncbi.nlm.nih.gov/pubmed/36992075
http://dx.doi.org/10.4274/jtgga.galenos.2023.2022-8-10
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