2018.4-25.Buschke


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EL Jouari O, Zaougui A, Gallouj S, Farih MH, Mernissi FZ. Buschke-Loewenstein tumor. Our Dermatol Online. 2018;9(4):453-453.

 

 
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The Buschke-Loewenstein tumor

Ouiame EL Jouari1, Anas Zaougui2, Ghita Senhaji1, Salim Gallouj1, Moulay Hassan Farih2, Fatima Zahra Mernissi1

1Department of Dermatology, University Hospital Hassan II Fez, Morocco, 2Department of Urology, University Hospital Hassan II Fez, Morocco

Corresponding author: Dr. Ouiame EL Jouari, E-mail: eljouariouiame@gmail.com

Submission: 27.05.2018; Acceptance: 09.08.2018

DOI: 10.7241/ourd.20184.25

A 26-year-old patient had a verrucous lesion on the genital region. She reported a progressive growth of this lesions during the last 3 years and prurit. Clinical examination revealed a 6 cm tumor of the vulva with a verrucous surface, irregular contours and non-infiltrated base and no palpable adenopathies (Fig. 1). The diagnosis of Buschke-Loewenstein tumor was clinically retained and the patient was referred to the urology department for surgical excision.

Figure 1: A 6 cm skin color tumor of the vulva with a verrucous surface and irregular contours.

 

The Buschke-Loewenstein tumor is a rare sexually transmitted disease. It is caused by subtypes 6 and 11 of the human papillomavirus (HPV) and characterized by excessive growth of verrucous lesions on the genitals and/or perianal region. The risk of recurrence and degenerescence is very important. the main treatment is surgical excision.

CONSENT

The examination of the patient was conducted according to the Declaration of Helsinki principles.

Notes

Source of Support: Nil

Conflict of Interest: None declared.


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