Edwards S L, Blessing K
Department of Pathology, Aberdeen University, Foresterhill, UK.
J Clin Pathol. 2000 Jun;53(6):409-18. doi: 10.1136/jcp.53.6.409.
A number of pigmented lesions are difficult to classify and raise the possibility of a melanoma diagnosis. Care should be exercised to exclude non-melanocytic lesions, and benign melanocytic entities, both of which can mimic melanoma histologically. In addition, the possibility of the lesion being a melanoma variant or epidermotropic metastasis should be considered. There will still be some cases that are difficult to resolve. These usually fall into one of three categories: atypical junctional melanocytic lesion versus early melanoma; naevus versus naevoid melanoma; and atypical Spitz, cellular blue, and deep penetrating naevi versus thick melanoma. These will pose problems even for experts. The atypical Spitz lesions are perhaps the most important category because they tend to be from younger individuals, the differential diagnosis is thick melanoma, and there is no single discriminating histological feature.
一些色素沉着性病变难以分类,增加了黑色素瘤诊断的可能性。应谨慎排除非黑素细胞性病变和良性黑素细胞性病变,这两者在组织学上都可能模仿黑色素瘤。此外,应考虑病变为黑色素瘤变体或亲表皮转移的可能性。仍会有一些病例难以解决。这些病例通常分为三类:非典型交界性黑素细胞病变与早期黑色素瘤;痣与痣样黑色素瘤;非典型斯皮茨痣、细胞性蓝痣和深部穿透性痣与厚黑色素瘤。即使对专家来说,这些也会带来问题。非典型斯皮茨病变可能是最重要的一类,因为它们往往发生在较年轻的个体,鉴别诊断是厚黑色素瘤,而且没有单一的鉴别组织学特征。