The clinical and dermoscopic features of invasive cutaneous squamous cell carcinoma depend on the histopathological grade of differentiation

医学 病理 细胞分化 优势比 基底细胞 生物 生物化学 基因
作者
Aimilios Lallas,John H. Pyne,Αthanassios Kyrgidis,Sebastián Andreani,Giuseppe Argenziano,Armando Radesca Cavaller,Jason Giacomel,Caterina Longo,A. Malvestiti,Elvira Moscarella,Simonetta Piana,Francesca Specchio,Rainer Hofmann‐Wellenhof,Iris Zalaudek
出处
期刊:British Journal of Dermatology [Oxford University Press]
卷期号:172 (5): 1308-1315 被引量:100
标识
DOI:10.1111/bjd.13510
摘要

Little is known about the variability of the dermoscopic criteria of squamous cell carcinoma (SCC) according to the histopathological differentiation grade.To evaluate whether specific dermoscopic criteria can predict the diagnosis of poorly differentiated SCC compared with well- and moderately differentiated SCC.Clinical and dermoscopic images of SCCs were retrospectively evaluated for the presence of predefined criteria. Univariate and adjusted odds ratios were calculated. Discriminant functions were used to plot receiver-operator characteristic curves.Of 143 SCCs included, 48 (33·5%) were well differentiated, 45 (31·5%) were moderately differentiated and 50 (35·0%) were poorly differentiated. Flat tumours had a fourfold increased probability of being poorly differentiated. Dermoscopically, the presence of a predominantly red colour posed a 13-fold possibility of poor differentiation, whereas a predominantly white and white-yellow colour decreased the odds of poorly differentiated SCC by 97% each. The presence of vessels in more than 50% of the tumour's surface, a diffuse distribution of vessels and bleeding were significantly associated with poor differentiation, while scale/keratin was a potent predictor of well- or moderately differentiated tumours.Dermoscopy may be regarded as a reliable preoperative tool to distinguish poorly from well- and moderately differentiated SCC. Given that poor differentiation of SCC represents an independent risk factor for recurrence, metastasis and disease-specific death, identifying poorly differentiated tumours in vivo may enhance their appropriate management.

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