Benign melanocytic tumor in infancy: Discussion on a rare case and review of the literature

被引:22
作者
Oruckaptan, HH [1 ]
Soylemezoglu, F
Kutluk, T
Akalan, N
机构
[1] Hacettepe Univ, Sch Med, Dept Neurosurg, TR-06100 Ankara, Turkey
[2] Hacettepe Univ, Sch Med, Dept Pathol, Ankara, Turkey
[3] Hacettepe Univ, Sch Med, Dept Pediat, Div Oncol, Ankara, Turkey
关键词
melanocytes; meningeal neoplasm; melanotic meningioma; meningeal melanocytoma; pigmented neoplasms;
D O I
10.1159/000028945
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Meningeal melanocytoma is an infrequent neoplasm of the central nervous system (CNS), especially in childhood and infancy. It was first described as an entity different from pigmented meningiomas and schwannomas in 1972, and few cases have been published so far, in this article, a 5-month-old male patient with meningeal melanocytoma is presented. This midline lesion was localized in the posterior fossa and manifested by hydrocephalus. The entire dural origin and extradural growing pattern in addition to the destruction of the adjacent occipital bone were the unexpected presentations since these tumors usually tend to locate on leptomeninges and to extend into the adjacent neural compartment rather than the outside. On the other hand, this case is the only one which had identical lesions in both surrenal glands and the left renal capsule, the structures containing neural-crest-derived cells outside the CNS. The prognostic criteria, differential diagnosis and its embryological aspects are discussed with an extensive review of the related existing literature. Copyright (C) 2000 S. Karger AG, Basel.
引用
收藏
页码:240 / 247
页数:8
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