Cargando…

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,...

Descripción completa

Detalles Bibliográficos
Autores principales: Boda, Daniel, Cutoiu, Ana, Bratu, Dalia, Bejinariu, Nona, Crutescu, Rodica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
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
_version_ 1784695645092708352
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
work_keys_str_mv AT bodadaniel buschkelowensteintumorsaseriesof7casereports
AT cutoiuana buschkelowensteintumorsaseriesof7casereports
AT bratudalia buschkelowensteintumorsaseriesof7casereports
AT bejinariunona buschkelowensteintumorsaseriesof7casereports
AT crutescurodica buschkelowensteintumorsaseriesof7casereports