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[神经皮肤黑素沉着症]

[Neurocutaneous melanosis].

作者信息

Díaz-Insa S, Pineda M, Bestué M, Espada F, Alvarez-Fernández E

机构信息

Servicio de Neurologia, Hospital Sant Joan de Déu, Barcelona, España.

出版信息

Rev Neurol. 1998 May;26(153):769-71.

PMID:9634665
Abstract

INTRODUCTION

Neurocutaneous melanosis is an infrequent condition characterized by the presence of numerous gigantic cutaneous naevi and melanocytic infiltration of the central nervous system and/or the leptomeningeal layers. Different clinical features may be seen: endocranial hypertension due to hydrocephalus, cranial nerve paralysis, myelopathy, convulsive seizures, etc. The prognosis is considered to be malignant. Only positive CNS histological findings confirm the diagnosis.

CLINICAL CASE

We present the case of a man with cutaneous lesions compatible with the diagnosis of neurocutaneous melanosis since birth, with benign self-limiting epilepsy in early childhood. Cerebral CT and MR scans were normal until the age of 17, when hipper-signal lesions appeared on MR, infiltrating the leptomeninges of the deep temporal pole and anterior aspect of the cerebral peduncles, which suggested the presence of melanocytes in the CNS.

CONCLUSIONS

There are cases of neurocutaneous melanosis with a good medium-term prognosis and benign manifestations until infiltration of the CNS occurs. Then they start to show the classical behavior of cases with a malignant prognosis. MR should be included as part of the diagnostic criteria for neurocutaneous melanosis. MR should be done periodically in patients with cutaneous lesions suggestive of this condition.

摘要

引言

神经皮肤黑素沉着症是一种罕见病症,其特征为存在大量巨大皮肤痣以及中枢神经系统和/或软脑膜层的黑素细胞浸润。可观察到不同的临床特征:因脑积水导致的颅内高压、脑神经麻痹、脊髓病、惊厥发作等。其预后被认为是恶性的。只有中枢神经系统组织学检查结果呈阳性才能确诊。

临床病例

我们报告一例自出生就有符合神经皮肤黑素沉着症诊断的皮肤病变的男性病例,该患者在幼儿期有良性自限性癫痫。直到17岁,脑部CT和磁共振成像(MR)扫描结果均正常,之后MR出现高信号病变,浸润颞叶深部极和脑桥前部的软脑膜,提示中枢神经系统存在黑素细胞。

结论

存在一些神经皮肤黑素沉着症病例,在中枢神经系统发生浸润之前,中期预后良好且表现为良性。之后它们开始呈现出预后恶性病例的典型表现。MR应纳入神经皮肤黑素沉着症的诊断标准。对于有提示该病的皮肤病变的患者,应定期进行MR检查。

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