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口腔增殖性疣状白斑的恶性转化:48 例患者系列及治疗建议。

Malignant transformation of oral proliferative verrucous leukoplakia: a series of 48 patients with suggestions for management.

机构信息

Department of Interdisciplinary Medicine, University of Bari, Bari, Italy.

Department of Emergency and Organ Transplantation, University of Bari, Bari, Italy.

出版信息

Int J Oral Maxillofac Surg. 2021 Jan;50(1):14-20. doi: 10.1016/j.ijom.2020.05.019. Epub 2020 Jun 23.

Abstract

Proliferative verrucous leukoplakia (PVL) is a rare and refractory form of oral mucosal leukoplakia of unknown origin, characterized by high rates of malignant transformation. Different diagnostic criteria, terminologies, and therapeutic approaches have been proposed since the first report in 1985. There remains no general agreement regarding the clinical and histological diagnosis, prevention, and correct management of this disease. This retrospective study investigated 48 patients affected by PVL showing at least one malignant transformation and followed up at 2-month intervals. Twenty-five were female (52.1%) and 23 (47.9%) were male; their median age was 67 years (range 40-93 years). Follow-up ranged from 18 to 240 months. Clinical examination included the use of Lugol's solution to prevent clinical underestimation of the margins and toluidine blue for suspicious areas. Surgical excision by scalpel was the preferred treatment for suspicious lesions, with only five carcinomas surgically removed by diode laser and two by CO laser. All specimens were accurately mapped after formalin fixation. Fifteen patients (31.3%; 10 female, five male) developed one oral carcinoma, while 33 (68.7%) developed two or more primary tumours (range 3-12). Only four patients (8.3%), who developed between 2 and 8 oral squamous cell carcinomas (OSCCs), died of tumour-related causes. The pre-surgical clinical workup, subsequent surgical treatment, and follow-up are key to success for patients affected by PVL with malignant transformation into stage 1 OSCC and/or verrucous carcinoma, leading to a high overall survival rate.

摘要

增殖性疣状白斑(PVL)是一种罕见的、难治性的口腔黏膜白斑病,其病因不明,恶性转化率高。自 1985 年首次报道以来,已经提出了不同的诊断标准、术语和治疗方法。对于这种疾病的临床和组织学诊断、预防和正确管理,仍然没有达成普遍共识。本回顾性研究调查了 48 例至少有一次恶变且随访间隔为 2 个月的 PVL 患者。25 例为女性(52.1%),23 例为男性(47.9%);中位年龄为 67 岁(范围 40-93 岁)。随访时间为 18-240 个月。临床检查包括使用卢戈氏液以防止临床低估边缘和甲苯胺蓝检查可疑区域。手术刀切除是可疑病变的首选治疗方法,只有 5 例癌变通过二极管激光和 2 例通过 CO 激光手术切除。所有标本在福尔马林固定后均准确绘制。15 例(31.3%;10 例女性,5 例男性)发生 1 例口腔癌,33 例(68.7%)发生 2 例或更多原发性肿瘤(范围 3-12)。只有 4 例(8.3%)患者发生 2-8 例口腔鳞状细胞癌(OSCC),因肿瘤相关原因死亡。对于发生 1 期 OSCC 和/或疣状癌恶变的 PVL 患者,术前临床检查、后续手术治疗和随访是成功的关键,可获得较高的总生存率。

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