Ito H, Akagi O, Nomura N, Tahara E
Section of Clinical Pathology, Kure Mutual Aid Hospital, Japan.
Histopathology. 1988 Aug;13(2):181-9. doi: 10.1111/j.1365-2559.1988.tb02023.x.
A case of giant pigmented tumour of the scalp which developed in a 47-year-old woman is reported. Macroscopically, the tumour showed a peculiar two-layered structure, consisting of an upper non-pigmented and a lower pigmented portion. Histologically, it was composed of elongated neurofibromatous tumour cells with abundant collagen fibres in the non-pigmented portion and round naevus-like cells with abundant melanin pigment in the pigmented portion. S-100 protein and neurone-specific enolase were demonstrated in most of the tumour cells, but neurofilament and myelin basic protein were not detected. Electron microscopy revealed melanosomes in the tumour cells of the pigmented portion. These findings might support a melanocytic origin for the tumour, but the lack of superficial pigmentation and the associated hair loss were against this. The tumour may represent an example of duality of neural crest differentiation.
报告了一例发生在一名47岁女性头皮的巨大色素性肿瘤。大体上,肿瘤呈现出一种特殊的两层结构,由上层无色素部分和下层色素部分组成。组织学上,无色素部分由含有丰富胶原纤维的细长神经纤维瘤样肿瘤细胞组成,色素部分由含有丰富黑色素的圆形痣样细胞组成。大多数肿瘤细胞中检测到S-100蛋白和神经元特异性烯醇化酶,但未检测到神经丝和髓鞘碱性蛋白。电子显微镜检查显示色素部分的肿瘤细胞中有黑素小体。这些发现可能支持肿瘤起源于黑素细胞,但缺乏表面色素沉着和相关脱发情况与之不符。该肿瘤可能代表神经嵴分化二元性的一个例子。