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Buschke-Löwenstein tumors: A series of 7 case reports
Giant condyloma acuminatum (GCA), or Buschke-Löwenstein tumor (BLT), represents an infrequent sexually transmitted disease (STD), caused by human papillomavirus (HPV), especially genotype 6 or 11. There are numerous risk factors for HPV, such as multiple sexual partners, homosexuality, prostitution,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047027/ https://www.ncbi.nlm.nih.gov/pubmed/35495587 http://dx.doi.org/10.3892/etm.2022.11320 |
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author | Boda, Daniel Cutoiu, Ana Bratu, Dalia Bejinariu, Nona Crutescu, Rodica |
author_facet | Boda, Daniel Cutoiu, Ana Bratu, Dalia Bejinariu, Nona Crutescu, Rodica |
author_sort | Boda, Daniel |
collection | PubMed |
description | Giant condyloma acuminatum (GCA), or Buschke-Löwenstein tumor (BLT), represents an infrequent sexually transmitted disease (STD), caused by human papillomavirus (HPV), especially genotype 6 or 11. There are numerous risk factors for HPV, such as multiple sexual partners, homosexuality, prostitution, chronic genital infections, as well as the lack of proper hygiene. HPV infection is a field infection, where large areas of cells at a tissue surface are affected by the HPV virus; therefore, once the GCA is excised, treatment of the whole affected genital area needs to be undertaken. The treatment is classified into topical therapy (podophyllin, 5-FU, radiotherapy, topical photodynamic therapy), excisional therapy (CO(2) laser, cryotherapy, electrotherapy, surgery) and immunotherapy (imiquimod). However, the ‘gold standard’ therapy is represented by wide surgical excision without grafting, since it is considered that healing per secundam is an improved approach, because there is no risk of recurrences on fibrotic tissue. A total of 7 cases of the BLT with comorbidities and particularities are presented and it is recommended that it be taken into consideration that the incidence of the disease is increasing, emphasizing the importance of an early diagnosis, as well as an adequate treatment. |
format | Online Article Text |
id | pubmed-9047027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-90470272022-04-29 Buschke-Löwenstein tumors: A series of 7 case reports Boda, Daniel Cutoiu, Ana Bratu, Dalia Bejinariu, Nona Crutescu, Rodica Exp Ther Med Case Report Giant condyloma acuminatum (GCA), or Buschke-Löwenstein tumor (BLT), represents an infrequent sexually transmitted disease (STD), caused by human papillomavirus (HPV), especially genotype 6 or 11. There are numerous risk factors for HPV, such as multiple sexual partners, homosexuality, prostitution, chronic genital infections, as well as the lack of proper hygiene. HPV infection is a field infection, where large areas of cells at a tissue surface are affected by the HPV virus; therefore, once the GCA is excised, treatment of the whole affected genital area needs to be undertaken. The treatment is classified into topical therapy (podophyllin, 5-FU, radiotherapy, topical photodynamic therapy), excisional therapy (CO(2) laser, cryotherapy, electrotherapy, surgery) and immunotherapy (imiquimod). However, the ‘gold standard’ therapy is represented by wide surgical excision without grafting, since it is considered that healing per secundam is an improved approach, because there is no risk of recurrences on fibrotic tissue. A total of 7 cases of the BLT with comorbidities and particularities are presented and it is recommended that it be taken into consideration that the incidence of the disease is increasing, emphasizing the importance of an early diagnosis, as well as an adequate treatment. D.A. Spandidos 2022-06 2022-04-13 /pmc/articles/PMC9047027/ /pubmed/35495587 http://dx.doi.org/10.3892/etm.2022.11320 Text en Copyright: © Boda et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Case Report Boda, Daniel Cutoiu, Ana Bratu, Dalia Bejinariu, Nona Crutescu, Rodica Buschke-Löwenstein tumors: A series of 7 case reports |
title | Buschke-Löwenstein tumors: A series of 7 case reports |
title_full | Buschke-Löwenstein tumors: A series of 7 case reports |
title_fullStr | Buschke-Löwenstein tumors: A series of 7 case reports |
title_full_unstemmed | Buschke-Löwenstein tumors: A series of 7 case reports |
title_short | Buschke-Löwenstein tumors: A series of 7 case reports |
title_sort | buschke-löwenstein tumors: a series of 7 case reports |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047027/ https://www.ncbi.nlm.nih.gov/pubmed/35495587 http://dx.doi.org/10.3892/etm.2022.11320 |
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