buschke - lowenstein的肿瘤管理

A. Lévy (Chef de clinique) , C. Lebbe (Professeur des Universités, praticien hospitalier)
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引用次数: 27

摘要

Buschke-Löwenstein肿瘤分类为疣状癌。它表现为生殖器或肛门周围的外生性肿瘤,伴有溃疡,有时有瘘管和鼻窦。它优先见于男性和免疫功能低下的患者。组织学表现与尖锐湿疣相似,但有压迫和移位深层组织的倾向,无基底膜破坏。HPV 6型或11型通常与该肿瘤有关。其他STI必须搜索。体格检查和精确影像学检查有助于选择正确的治疗方案。建议根治性切除以避免恶性转化,但由于复发率高,必须大面积切除。其他治疗方式,如化疗或咪喹莫特,可能是有益的,以避免致残手术干预。由于经常复发和可能发生恶性转化,定期随访是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prise en charge des tumeurs de Buschke-Löwenstein

Buschke-Löwenstein tumour is classified as a verrucous carcinoma. It presents like an exophytic tumour of the genital or peri-anal area, with ulceration and sometimes fistulae and sinuses. It is preferentially seen in men and immunocompromised patients. Histological appearance is not far from condyloma acuminata, but with a tendency to compress and displace deeper tissues, without basement membrane disruption. HPV types 6 or 11 are regularly found in association with this tumour. Other STI have to be searched. Physical examination and precise imagery are useful to chose the right treatment regimen. Radical excision is recommended to avoid malignant transformation, but has to be large because of the high number of recurrences. Other treatment modalities such as chemotherapy or imiquimod could be of interest to avoid mutilating surgical interventions. A regular follow-up is necessary because of frequent recurrences and possible malignant transformation.

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来源期刊
Annales D Urologie
Annales D Urologie 医学-泌尿学与肾脏学
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