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[下丘脑错构瘤中的痴笑性癫痫和性早熟]

[Gelastic epilepsy and precocious puberty in hamartoma of the hypothalamus].

作者信息

Dammann O, Commentz J C, Valdueza J M, Christante L, Bentele K H

机构信息

Universitätskinderklinik Hamburg-Eppendorf.

出版信息

Klin Padiatr. 1991 Nov-Dec;203(6):439-47. doi: 10.1055/s-2007-1025470.

Abstract

Four cases of hypothalamic hamartoma leading to gelastic epilepsy, precocious puberty and behavioural disorders are reported. Cerebral neuroradiologic examinations revealed a tumor-like mass attached to the hypothalamus in the region of the mamillary bodies in all cases. Precocious puberty developed in the two girls at 4 and 13 months but in neither of the two boys, who both suffered behaviour disturbances in the form of aggressive outbursts. A total resection of the tumors of both boys led to histologic confirmation of hamartoma. One boy was free of seizures upon follow-up, whereas seizure frequency in the other boy was reduced, while his aggressivity increased. The cases are discussed in context of current therapeutic conceptions of gelastic epilepsy and central precocious puberty.

摘要

报告了4例导致痴笑性癫痫、性早熟和行为障碍的下丘脑错构瘤病例。所有病例的脑部神经放射学检查均显示,在乳头体区域有一个附着于下丘脑的肿瘤样肿块。两名女孩分别在4个月和13个月时出现性早熟,但两名男孩均未出现,他们都有攻击性行为形式的行为障碍。两名男孩的肿瘤均被完全切除,组织学证实为错构瘤。一名男孩在随访时无癫痫发作,而另一名男孩的癫痫发作频率降低,但攻击性增加。结合当前对痴笑性癫痫和中枢性性早熟的治疗观念对这些病例进行了讨论。

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