Buschke-Löwenstein瘤：罕见的双侧定位。
Buschke Lowenstein tumor: unusual bilateral localization.
作者信息
Ali Sbai Mohamed, Balti Walid, Dhahak Slim, Ben Romdhane Selma, Tabib Massoued, Balti Hedi
机构信息
Department of Orthopaedic Surgery, Maamouri Hospital, Nabeul.
出版信息
Tunis Med. 2009 Sep;87(9):627-9.
BACKGROUND
The tumor of buschke lowenstein or giant condyloma acuminata is a pseudo-épitheliomatous profileration bilonging to verrucous carcinoma group due to their aggressive local evolution. A malignant change as micro invasive carcinoma or epidermoid kératinizing carcinoma well-differentiated was reported. Diagnosis and surgical treatment represents an efficient alternative at the moment that must be precocius and large due to the frequencies of local recurrences and malignant change.
AIM
We present in this stady an observation of an unusual localization of buschke Lowenstein tumor with review of literature.
CASE REPORT
50-year-old men presented with bilateral tumours in the battock area whose diagnosis of buschke Lowenstein tumour has been clinically suspected and confirmed by biopsy and histopathologic study. The cover has been achieved by VY fasciocutaneous flaps of the muscle gluteus maximus.
背景
Buschke-Löwenstein肿瘤或巨大尖锐湿疣是一种假上皮瘤样增生，因其局部侵袭性生长而属于疣状癌组。有报道称其可发生微侵袭癌或高分化表皮角化癌等恶性转变。由于局部复发和恶性转变的发生率，诊断和手术治疗目前是一种有效的选择，且必须早期进行且范围要大。
目的
我们在本研究中报告一例Buschke-Löwenstein肿瘤不寻常部位的观察病例并复习文献。
病例报告
一名50岁男性，臀部区域出现双侧肿瘤，临床怀疑为Buschke-Löwenstein肿瘤，并经活检和组织病理学研究确诊。通过臀大肌VY筋膜皮瓣完成覆盖。
Zotero 插件