Giant condyloma acuminatum
(Redirected from Buschke–Löwenstein tumor)
Giant condyloma acuminatum (GCA), also known as Buschke-Löwenstein tumor, is a rare and aggressive variant of condyloma acuminatum that predominantly affects the genital, anal, and perianal regions. It is characterized by its large size, verrucous appearance, and potential for local invasive growth. Despite its aggressive nature, GCA is considered a benign condition, although it has a high risk of progressing to squamous cell carcinoma if left untreated.
Etiology and Pathogenesis[edit | edit source]
GCA is primarily caused by infection with certain types of Human papillomavirus (HPV), particularly HPV types 6 and 11, which are also associated with the more common anogenital warts. The transformation from a typical condyloma acuminatum to a giant form is not fully understood but is thought to involve factors such as immunosuppression, chronic irritation, and poor hygiene.
Clinical Features[edit | edit source]
Patients with GCA typically present with a large, cauliflower-like mass in the genital, anal, or perianal area. The lesion may be accompanied by symptoms such as pain, itching, bleeding, and foul-smelling discharge. Due to its size and location, GCA can interfere with urination, defecation, and sexual function, significantly impacting the patient's quality of life.
Diagnosis[edit | edit source]
The diagnosis of GCA is primarily clinical, based on the appearance of the lesion. However, biopsy and histopathological examination are necessary to confirm the diagnosis and to rule out malignancy. Imaging studies, such as MRI or CT scans, may be used to assess the extent of the lesion and its potential invasion into surrounding tissues.
Treatment[edit | edit source]
Treatment of GCA is challenging and often requires a multidisciplinary approach. Options include surgical excision, which is the most definitive treatment, and medical therapies such as topical or systemic chemotherapy and immunotherapy. Laser therapy and radiotherapy have also been used in some cases. Due to the high risk of recurrence, close follow-up is essential.
Prognosis[edit | edit source]
The prognosis of GCA depends on the extent of the disease and the success of treatment. Early diagnosis and complete excision of the lesion are associated with a better outcome. However, the risk of recurrence is high, and there is a potential for malignant transformation into squamous cell carcinoma, which can significantly worsen the prognosis.
Prevention[edit | edit source]
Prevention of GCA involves the reduction of risk factors for HPV infection, such as practicing safe sex and avoiding multiple sexual partners. Vaccination against HPV is also an effective preventive measure, although it is not yet clear whether it can specifically prevent GCA.
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Contributors: Prab R. Tumpati, MD