Buschke-Löwenstein Tumor

report of three cases

Authors

  • Mayra Cavalcante Gazelli Universidade Federal do Ceará (UFC)
  • Iago Farias Jorge
  • Muse de Oliveira Santiag
  • Karinne Cisne Fernandes Rebouças Universidade Federal do Ceará (UFC)
  • Diane Isabelle Magno Cavalcante Universidade Federal do Ceará (UFC)
  • Raquel Autran Coelho Universidade Federal do Ceará (UFC)

Keywords:

Buschke-Lowenstein tumor, Condylomata Acuminata, Papillomaviridae

Abstract

The Buschke-Löwenstein Tumor is a rare, sexually transmitted disease, triggered by human papillomavirus, specially the subtypes 6 and 11. It is characterized as a cauliflower-shape exophytic mass, slowly progressive, with high local recurrence rates and high infiltration. The main risk factor is immunosuppression. Surgical treatment is usually preferred, with or without adjuvant therapy. It has a great impact on the patients’ life, impairing their life quality. We report three cases of Giant Condyloma with diverse histopathological findings with varying degrees of infiltration and papillomatosis. 

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Author Biographies

Karinne Cisne Fernandes Rebouças, Universidade Federal do Ceará (UFC)

Sexually Transmitted Infections Service of Maternidade-Escola Assis Chateaubriand of the UFC – Fortaleza (CE), Brazil.

Diane Isabelle Magno Cavalcante, Universidade Federal do Ceará (UFC)

Pathology and Forensic Medicine Department of the UFC – Fortaleza (CE), Brazil.

Raquel Autran Coelho, Universidade Federal do Ceará (UFC)

Mother and Child Health Department of the UFC – Fortaleza (CE), Brazil.

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Published

2017-03-05

How to Cite

1.
Gazelli MC, Jorge IF, Santiag M de O, Rebouças KCF, Cavalcante DIM, Coelho RA. Buschke-Löwenstein Tumor: report of three cases. DST [Internet]. 2017 Mar. 5 [cited 2024 Dec. 17];29(2):67-9. Available from: https://bdst.emnuvens.com.br/revista/article/view/1148

Issue

Vol. 29 No. 2 (2017)

Section

Case Report