Reiter Ofer, Mimouni Tomer, Scope Alon, Kurtansky Nicholas R, Pastore Larissa, Halpern Allan C, Marghoob Ashfaq A
Dermatology Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
School of Medicine, Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
J Eur Acad Dermatol Venereol. 2024 Dec 16. doi: 10.1111/jdv.20503.
When monitoring melanocytic neoplasms, the pattern of change may distinguish nevi from melanoma. Anticipating the growth dynamics of nevi based on their dermoscopic pattern is important to make this distinction.
The primary aim was to examine the association between nevus dermoscopic pattern at baseline and diameter change during long-term monitoring. The secondary aim was to examine the association between nevus dermoscopic pattern at baseline and changes in both dermoscopic pattern and colour during long-term monitoring.
The study included high-risk adult patients that underwent ≥2 total-body photography (TBP) sessions, with at least 14 years' time gap between first and last sessions. Nevi on the torso, with available dermoscopic images, were included. New and disappearing nevi were defined as nevi not appearing on the first and last TBP, respectively. Nevus diameter and colour were assessed on clinical images of first and last TBP images. Dermoscopic images were analysed for dermoscopic patterns and structures at baseline and follow-up.
In total, 877 nevi from 101 patients were included. Mean follow-up time between TBPs and between dermoscopic images was 16.7 and 11.5 years, respectively. Most nevi were reticular or structureless at baseline, but new nevi had a higher frequency of peripheral globules and smudgy patterns. Peripheral globules and diffuse negative network patterns as well as regression structures were associated with nevus diameter growth. In total, 30% and 15% of new and existing nevi, respectively, demonstrated dermoscopic pattern change, mainly transforming into reticular and structureless patterns.
Among high-risk patients, nevi showing peripheral globules or negative network are more likely to grow in diameter during long-term monitoring. Most nevi retain their overall dermoscopic pattern and those that change, mostly transform into reticular or structureless patterns.
在监测黑素细胞肿瘤时,变化模式可区分痣和黑色素瘤。基于其皮肤镜模式预测痣的生长动态对于做出这种区分很重要。
主要目的是研究基线时痣的皮肤镜模式与长期监测期间直径变化之间的关联。次要目的是研究基线时痣的皮肤镜模式与长期监测期间皮肤镜模式和颜色变化之间的关联。
该研究纳入了接受≥2次全身摄影(TBP)的高危成年患者,首次和最后一次摄影之间至少间隔14年。纳入躯干上有可用皮肤镜图像的痣。新出现和消失的痣分别定义为在第一次和最后一次TBP上未出现的痣。在第一次和最后一次TBP图像的临床图像上评估痣的直径和颜色。分析皮肤镜图像的基线和随访时的皮肤镜模式和结构。
总共纳入了101例患者的877颗痣。TBP之间以及皮肤镜图像之间的平均随访时间分别为16.7年和11.5年。大多数痣在基线时为网状或无结构,但新痣的周边小球和模糊模式频率更高。周边小球和弥漫性负网络模式以及消退结构与痣直径增长相关。总共分别有30%的新痣和15%的现有痣出现皮肤镜模式变化,主要转变为网状和无结构模式。
在高危患者中,显示周边小球或负网络的痣在长期监测期间更有可能直径增大。大多数痣保持其整体皮肤镜模式,而那些发生变化的痣大多转变为网状或无结构模式。