Unusual Dermoscopic Patterns of Basal Cell Carcinoma Mimicking Melanoma
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Unusual Dermoscopic Patterns of Basal Cell Carcinoma Mimicking Melanoma
Abstract:
Background: Basal cell carcinoma can simulate melanoma and specific dermoscopic criteria have not yet been defined in a large cohort.
Objective: To identify dermoscopic “trump” characteristics for differential diagnosis, identify cluster groups and assess the clinical impact of this study’s findings.
Methods: Retrospective, multicentric comparative study of atypical, non-facial basal cell carcinoma (≥1 seven-point checklist criteria) and melanoma (with at least one BCC criteria) at dermoscopy. Observed dermoscopic features were used to develop a proposed score. Lesion clusters were defined with hierarchical analysis. Clinical impact was assessed with a blinded reader study (diagnostic accuracy and confidence) following this study’s results.
Results: A total of 146 basal cell carcinoma and 76 melanoma were included. Atypical vascular pattern was common to most lesions (74.5%). Twelve trump features were included in the proposed score (sensitivity 94.1% and specificity 79.5%). Cluster analysis identified 3 basal cell carcinoma and 3 melanoma clusters. Findings improved overall diagnostic accuracy and confidence (26.8% and 13.8% respectively; p<0.001).
Limitations: Retrospective design and proposed score unvalidated.
Conclusions: Atypical vascular pattern should no longer be considered a melanoma associated feature only. Our proposed score improves diagnostic accuracy and confidence. Absence of pigmented features were associated with lower diagnostic accuracy and confidence.
Figure legends
Figure S1.BCC l Lesions representative of the hypo/amelanotic-MM like cluster: (a-c-e) clinical images;(b-d-f) white-red structureless areas (asterisk), (b-d-f) atypical vascular pattern (black circle), (b-d-f) superficial (short) fine telangiectasia (triangle), (b-d-f) ulceration (rectangle), (b-d-f) some arborizing vessels (arrows). ). MM, malignant melanoma; BCC, basal cell carcinoma.
Figure S2. BCC lesions representative of the mixed cluster: (a-c-e) clinical images; (b-f) superficial (short) fine telangiectasia (black triangle), (b-d-f) multiple blue-gray globules (asterisk), (b-d) atypical vascular pattern (white triangle), (b-f) white-red structureless areas (rectangle), (f) irregular dots/globules (arrows), (f) white streaks (circle). ). BCC, basal cell carcinoma.
Table legends
Table S1. Dermoscopic features classified according to common associations in literature with malignant melanoma (MM) and/or basal cell carcinoma (BCC) diagnoses
Table S2. Demographic and clinical details for the included patients.
模拟黑色素瘤(Melanoma)的基底细胞癌(Basal Cell Carcinoma)罕见皮肤镜模式
摘要:
背景:基底细胞癌(Basal Cell Carcinoma)可模拟黑色素瘤(Melanoma),目前尚无针对大队列人群的特异性皮肤镜诊断标准。
目的:明确可用于鉴别诊断的皮肤镜决定性特征,确定病变聚类分组,并评估本研究结果的临床应用价值。
方法:本研究为回顾性多中心对照研究,纳入经皮肤镜检查的非典型非面部基底细胞癌(满足≥1项七点评分检查表标准)及黑色素瘤(至少符合1项基底细胞癌诊断标准)病例。通过观察所得的皮肤镜特征拟定评分体系,采用层级聚类分析定义病变聚类组,并通过盲法阅片研究(诊断准确率与诊断置信度)评估本研究结果的临床应用价值。
结果:本研究共纳入146例基底细胞癌病例与76例黑色素瘤病例。非典型血管模式在多数病变中均可见(74.5%)。拟定的评分体系共纳入12项关键特征,灵敏度为94.1%,特异度为79.5%。聚类分析共识别出3组基底细胞癌病变与3组黑色素瘤病变。本研究结果可提升整体诊断准确率与诊断置信度(分别提升26.8%与13.8%;p<0.001)。
局限性:本研究为回顾性设计,且拟定的评分体系尚未经过验证。
结论:非典型血管模式不应再仅被视为黑色素瘤相关的特征。本研究拟定的评分体系可提升诊断准确率与置信度。无色素性特征与较低的诊断准确率及置信度相关。
图注:
图S1:模拟低色素/无色素性恶性黑色素瘤(Malignant Melanoma, MM)聚类的基底细胞癌(Basal Cell Carcinoma, BCC)病变:(a-c-e) 临床图像;(b-d-f) 白红色无结构区域(星号标注)、(b-d-f) 非典型血管模式(黑色圆圈标注)、(b-d-f) 浅表(短)细毛细血管扩张(三角标注)、(b-d-f) 溃疡(矩形标注)、(b-d-f) 部分树枝状血管(箭头标注)。其中MM为恶性黑色素瘤,BCC为基底细胞癌。
图S2:混合聚类代表性基底细胞癌(Basal Cell Carcinoma, BCC)病变:(a-c-e) 临床图像;(b-f) 浅表(短)细毛细血管扩张(黑色三角标注)、(b-d-f) 多发蓝灰色小球(星号标注)、(b-d) 非典型血管模式(白色三角标注)、(b-f) 白红色无结构区域(矩形标注)、(f) 不规则点状/球状结构(箭头标注)、(f) 白色条纹(圆圈标注)。其中BCC为基底细胞癌。
表注:
表S1:根据文献中与恶性黑色素瘤(Malignant Melanoma, MM)和/或基底细胞癌(Basal Cell Carcinoma, BCC)诊断相关的常见关联分类的皮肤镜特征
表S2:纳入研究患者的人口统计学与临床细节
创建时间:
2021-04-26



