Botticelli A R, Villani M, Angiari P, Peserico L
Cancer. 1983 Jun 15;51(12):2304-10. doi: 10.1002/1097-0142(19830615)51:12<2304::aid-cncr2820511223>3.0.co;2-u.
A case of meningeal melanocytoma of the left Meckel's cave associated with ipsilateral Ota's nevus in a 43-year-old woman, was studied by light and electron microscopy. The cells of the tumor were characterized by the presence of dendritic cytoplasmic processes, melanosomes and premelanosomes; hence, they were deemed as neoplastic melanocytes. Moreover, the tumor was lacking in histologic and ultrastructural features of pigmented meningioma, melanotic Schwannoma and primary meningeal melanoma. The prolonged clinical course was different from primary and metastatic malignant melanomas of the meninges. The best treatment appears to be radical excision, when possible; otherwise, the local or partial enucleation followed by radiation therapy has been found to be the best curative to date. On the whole, meningeal melanocytoma cannot be considered as entirely benign, given its morphologic patterns that resemble those of uveal melanoma, and its potential for recurrence. The association of this tumor with Ota's nevus is referred to as having a common origin from an arrested migration of melanoblasts at different stages.
对一名43岁女性的左侧梅克尔腔脑膜黑素细胞瘤合并同侧太田痣的病例进行了光镜和电镜研究。肿瘤细胞的特征是存在树突状细胞质突起、黑素小体和前黑素小体;因此,它们被视为肿瘤性黑素细胞。此外,该肿瘤缺乏色素性脑膜瘤、黑素性神经鞘瘤和原发性脑膜黑色素瘤的组织学和超微结构特征。其较长的临床病程与脑膜原发性和转移性恶性黑色素瘤不同。最佳治疗方法似乎是尽可能进行根治性切除;否则,目前发现局部或部分摘除后进行放射治疗是最佳的治疗方法。总体而言,鉴于脑膜黑素细胞瘤的形态学模式类似于葡萄膜黑色素瘤且有复发潜力,不能将其视为完全良性。这种肿瘤与太田痣的关联被认为起源于不同阶段黑素母细胞迁移停滞的共同起源。