应用数字皮肤镜筛检皮肤恶性黑色素瘤高危人群

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Background: Dermoscopy has improved the sensitivity and specificity of clinical diagnosis of melanoma from 60% to over 90% . However, in order not to miss melanoma a certain percentage of suspicious but benign lesions has to be excised. Objectives: To evaluate the dermoscopic changes and the rates of excision in benign melanocytic naevi and cutaneous malignant melanoma in long- term follow- up of high- risk patients using digital dermoscopy. Methods: Digital dermoscopic images of 2015 atypical melanocytic naevi in 196 high- risk patients were analysed retrospectively. Among others, the following data were collected for each naevus: changes in surface area, overall architecture, dermoscopic patterns and distribution of pigmentation. All tumours suspicious for melanoma or showing asymmetrical changes were excised. Results During a median follow- up time of 25 months 128 (6.4% ) of all naevi showed changes in size or architecture. Eighty- six per cent of all changes in patients who attended more than one visit were observed at the first follow- up visit. Thirty- three lesions showing changes were excised and two melanomas in situ and 31 melanocytic naevi were diagnosed. Conclusions: Follow- up examinations using digital dermoscopy revealed unchanged morphology in the large majority of melanocytic naevi. Excisions were only performed in cases of asymmetrical growth, asymmetrical changes of pigmentation, or development of dermoscopic features indicative of melanoma. The ratio of 33 lesions excised in order to identify two melanomas in situ seems reasonable and may be further reduced in future. Objective: To evaluate the dermoscopic changes and the rates of excision in benign melanocytic naevi and cutaneous malignant melanoma in long- term follow-up of high- risk patients using digital dermoscopy. Methods: Digital dermoscopic images of 2015 atypical melanocytic naevi in ​​196 high- risk patients were analyzed retrospectively. Among others, the following data were collected for each naevus: changes in surface area, overall architecture, dermoscopic patterns and distribution of pigmentation. All tumors suspicious for melanoma or showing asymmetrical changes were excised. Results During a median follow-up time of 25 months 128 (6.4%) of all naevi showed changes in size or architecture. Eighty- six per cent of all changes in patients who attend ed more than one visit were observed at the first follow-up visit. Thirty- three lesions showing changes were excised and two melanomas in situ and 31 melanocytic naevi were diagnosed. Conclusions: Follow-up examinations using digital dermoscopy revealed unchanged morphology in the large majority of melanocytic naevi. Excisions were performed only in cases of asymmetrical growth, asymmetrical changes of pigmentation, or development of dermoscopic features of melanoma. The ratio of 33 lesions excised in order to identify two melanomas in situ seems reasonable and may be further reduced in future.
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