作者: R. M. MacKie
DOI: 10.1046/J.1365-2230.2000.00692.X
关键词: Melanoma 、 Molecular marker 、 Pathology 、 Research setting 、 Medicine 、 Pathological
摘要: The four main clinicopathological subsets of melanoma are described and the arguments for their retention in a research setting presented. Further additional described, including partly regressed primary melanoma, arising congenital naevus multiple tumours. Pathological prognostic indicators discussed pre-eminent significance tumour thickness its interaction with ulceration described. need accurate personal predictive profiles as distinct from those relevant to populations is discussed, molecular marker metastatic potential.