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小脑发育异常性神经节细胞瘤(勒米特-迪克洛病)及其与多发性错构瘤综合征(考登病)的关系。

Dysplastic gangliocytoma of the cerebellum (Lhermitte-Duclos disease) and its relation to the multiple hamartoma syndrome (Cowden disease).

作者信息

Rimbau J, Isamat F

机构信息

Service of Neurosurgery, Hospital de Bellvitge, University of Barcelona, Spain.

出版信息

J Neurooncol. 1994;18(3):191-7. doi: 10.1007/BF01328953.

Abstract

The clinical manifestations, surgical treatment and postoperative results of three patients with gangliocytomas of the cerebellum (Lhermitte-Duclos disease) are presented. Particular attention is placed in one of the cases, that of a young woman with a short clinical history of episodic symptoms of intracranial hypertension, dizziness and ataxia, with a concomitant frontal meningioma and in the general context of a multiple hamartoma syndrome (Cowden disease). The possible relationship between both diseases is contemplated, since they can be the extremes of a wide spectrum of a peculiar form of phakomatosis.

摘要

本文介绍了3例小脑节细胞胶质瘤(Lhermitte-Duclos病)患者的临床表现、手术治疗及术后结果。其中1例为年轻女性,具有颅内高压、头晕和共济失调等发作性症状的短暂临床病史,同时伴有额叶脑膜瘤,且处于多发性错构瘤综合征(考登病)的背景下,对此病例给予了特别关注。考虑到这两种疾病可能存在的关系,因为它们可能是一种特殊形式的 phakomatosis广泛谱系的两端。

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