Mueller-Diesing Flurin, Stöth Manuel, Ludwig Elena, Rosenwald Andreas, Gerhard-Hartmann Elena, Moratin Helena, Gehrke Thomas, Goncalves Miguel, Scheich Matthias, Hackenberg Stephan, Scherzad Agmal, Meyer Till Jasper
Department of Oto-Rhino-Laryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery, University of Würzburg, Würzburg, Germany.
University of Würzburg, Institute of Pathology, Würzburg, Germany.
Laryngoscope. 2025 Sep;135(9):3296-3305. doi: 10.1002/lary.32200. Epub 2025 Apr 21.
Determining the prognosis of vocal fold leukoplakia remains challenging. The 2017 WHO Classification of Head and Neck Tumors proposed a two-tier grading system for classifying laryngeal precursor lesions. This resulted in the upstaging of "moderate dysplasia" to "high-grade dysplasia." The aim of this study was to retrospectively analyze the rates of malignant transformation in relation to the grade of dysplasia.
Totally, 392 patients who underwent at least one microlaryngoscopy with biopsy for laryngeal leukoplakia were included in this study. The rate and time to malignant transformation were analyzed according to the histopathological diagnosis and the localization of the leukoplakia.
Malignant transformation rates (defined as de novo occurrence of an invasive carcinoma) were low for hyperkeratosis or parakeratosis and mild dysplasia, but comparably high for moderate dysplasia, severe dysplasia, and carcinoma in situ (CIS) (6% vs. 9% vs. 41% vs. 43% vs. 55%). The time between first biopsy and malignant transformation varied widely (0.1-10.8 years) and did not show a significant dependence on the initial histopathological diagnosis.
Based on the observed malignant transformation rates, the data support classifying moderate dysplasia into the "high-grade" dysplasia group, in line with the fourth WHO classification from 2017. This implies that the clinical management of moderate dysplasia should align with that of severe dysplasia and CIS, involving histologically controlled resection.
确定声带白斑的预后仍然具有挑战性。2017年世界卫生组织头颈部肿瘤分类提出了一种两级分级系统,用于对喉前驱病变进行分类。这导致“中度发育异常”被上调为“高级别发育异常”。本研究的目的是回顾性分析发育异常分级与恶性转化发生率之间的关系。
本研究共纳入392例因喉白斑至少接受过一次显微喉镜检查及活检的患者。根据组织病理学诊断和白斑的定位分析恶性转化的发生率和时间。
角化过度或不全角化以及轻度发育异常的恶性转化发生率(定义为侵袭性癌的新发)较低,但中度发育异常、重度发育异常和原位癌(CIS)的发生率相对较高(分别为6%、9%、41%、43%和55%)。首次活检与恶性转化之间的时间差异很大(0.1 - 10.8年),且与初始组织病理学诊断无显著相关性。
基于观察到的恶性转化发生率,数据支持将中度发育异常归类为“高级别”发育异常组,这与2017年世界卫生组织第四次分类一致。这意味着中度发育异常的临床管理应与重度发育异常和原位癌的管理一致,包括组织学控制下的切除。