Giant condyloma acuminatum - Buschke-Lowenstein disease - a literature review.
نویسندگان
چکیده
AIM Buschke-Lowenstein disease or giant condyloma acuminatum represents a rare, sexually transmitted disorder, with a slow evolution and the tendency to infiltrate in the adjacent tissues; untreated, the outcome is unfavorable. The hallmark is the development of one or various prominent-sized vegetant tumors that usually ulcerate. MATERIAL AND METHODS The present article summarizes both the etiopathogenic features and the current approach of treatment management. RESULTS Minimally invasive surgery along with local and systemic therapy is adequate in patients with small-sized lesions or high intraoperative risk. The main treatment remains extensive surgery with wide resection and often reinterventions to complete the excision. CONCLUSIONS giant condyloma acuminatum represents a continuous surgical challenge, because of the need of exhaustive surgical procedures that should consider both the oncological principles and a better anatomical resolution. No standard treatment protocol can be established, because of the infrequency of the disease. Radical surgery including full thickness excision of the affected areas represents the "gold standard" therapy. Other known forms of treatment present unsatisfactory results without statistical significance, the studies having been conducted on small groups of patients. An adequate, long-term follow-up of Buschke-Lowenstein patients is highly recommended, because of the increased recurrence rate.
منابع مشابه
Perianal Giant Condyloma Acuminatum—Buschke-Löwenstein Tumor: A Case Report
Condyloma acuminatum caused by Human Papillomavirus is the most commonly occurring sexually transmitted infection in the anogenital region. Buschke-Löwenstein tumor (BLT) known also as giant condyloma acuminatum is a rare disease. The disease, for which the most important treatment method is the surgical excision, differs from normal condyloma acuminatum cases with its high degree of malignancy...
متن کاملتومور Buschke-Lowenstein ناشی از زگیل معمولی در آلت تناسلی (گزارش مورد)
تومور (BLT) Buschke-Lowenstein Tumor یا تومور گل کلمی شکل یا کوندیلوم آکومیناتوم بزرگ (GCA) Giant Condyloma Acuminatum با رشد آهسته و تهاجم موضعی است که اندازه بزرگی دارد و معمولاً در ناحیه پرینه ایجاد میشود. BLT توسط ویروس پاپیلومای انسانی، معمولاً توسط ژنوتیپ 6 یا 11 ایجاد میشود. BLT معمولاً در زمینه Condyloma Acuminatum ایجاد میشود و در هر سنی بعد از دوران بلوغ میتواند بروز کند. ولی معمولاً...
متن کاملVerrucous carcinoma arising in an extended giant condyloma acuminatum (Buschke–Löwenstein tumor): a case report and review of the literature
INTRODUCTION Verrucous carcinoma of the external genitalia and perianal region is a rare variant of well-differentiated squamous cell carcinoma. It has been reported to have limited metastatic potential. CASE PRESENTATION We report the case of a 54 year-old Moroccan man who presented with locally advanced giant condyloma acuminatum (Buschke-Löwenstein tumor) after prolonged intervals of negle...
متن کاملPerianal giant condyloma acuminatum (Buschke-Löwenstein tumor). Case report and review of the literature.
UNLABELLED Giant condyloma acuminatum, also known as Buschke-Löwenstein tumor (BLT) is a very rare sexually transmitted disease that affects the ano-genital region. BLT is a slow growing cauliflower-like tumor, but unlike simple condyloma, it is locally aggressive and destructive, malignant transformation occuring in 40-60% of cases. We present a case of perianal carcinomatous BLT and discuss s...
متن کاملGiant condyloma (Buschke-Löwenstein tumor). A case report.
Buschke-Löwenstein tumor (BLT), or giant condyloma acuminatum, is a rare sexually transmitted disease. The virus responsible for condyloma is human papillomavirus, usually serotype 6 or 11. A BLT is always preceded by condyloma acuminatum and may occur at any age after puberty. It is characterized by invasive growth and recurrence after treatment, and malignant transformation is possible. We re...
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ورودعنوان ژورنال:
- Chirurgia
دوره 109 4 شماره
صفحات -
تاریخ انتشار 2014