Bouhout Tariq, Ramdani Abdelbassir, Kharkhach Ayoub, Serji Badr
Surgical Oncology, Mohammed VI University Hospital, Regional Oncology Center, Oujda, MAR.
Cureus. 2024 Jan 21;16(1):e52700. doi: 10.7759/cureus.52700. eCollection 2024 Jan.
The Buschke-Löwenstein tumor is a rare clinical entity. Its severity is related to the local invasion and the risk of recurrence and malignant transformation. It is caused by a viral infection due to the human papillomavirus. The transmission is primarily sexual and often affects the penile region. The perineal location is relatively rare. We report two rare cases of neglected Buschke-Löwenstein tumor due to the late diagnosis treated with large surgical resection. This study aimed to emphasize the contribution of clinical examination in the early diagnosis and the management of our patients.
Buschke-Löwenstein肿瘤是一种罕见的临床实体。其严重程度与局部侵袭以及复发和恶变风险相关。它由人乳头瘤病毒引起的病毒感染所致。传播主要通过性途径,且常累及阴茎部位。会阴部位相对少见。我们报告两例因诊断延迟而被忽视的Buschke-Löwenstein肿瘤罕见病例,采用大手术切除进行治疗。本研究旨在强调临床检查在患者早期诊断和管理中的作用。