Veendrick-Meekes M J B M, Verhoeven W M A, van Erp M G, van Blarikom W, Tuinier S
Epilepsy Centre Kempenhaeghe, Heeze, The Netherlands.
Epilepsy Behav. 2007 Sep;11(2):218-21. doi: 10.1016/j.yebeh.2007.03.005. Epub 2007 Jul 2.
Hypothalamic hamartomas (HH) are developmental malformations that are associated with gelastic seizures, other types of seizures, cognitive decline, and symptoms related to hypothalamic dysfunction. Although aggressive behavior is frequently described, data on the neuropsychiatric profile are limited. In this article, five patients with HH are described who displayed a wide variety of psychiatric symptoms that, dependent on the time frame, met the criteria for several categorical diagnoses. Major neuropsychiatric symptoms comprised aggression that is only partial context dependent, compulsive behavior, psychotic symptoms not responding to treatment, and organic mood instability. HH should therefore be considered a neuropsychiatric syndrome with a highly variable expression that can be best captured by a thorough description of behaviors, symptoms, sequelae of epilepsy, and hypothalamic dysfunction.
下丘脑错构瘤(HH)是一种发育畸形,与痴笑性癫痫、其他类型的癫痫、认知衰退以及下丘脑功能障碍相关症状有关。尽管常描述有攻击性行为,但关于神经精神特征的数据有限。本文描述了5例HH患者,他们表现出各种各样的精神症状,根据时间框架不同,符合多种分类诊断标准。主要神经精神症状包括仅部分情境依赖的攻击行为、强迫行为、对治疗无反应的精神病性症状以及器质性情绪不稳定。因此,HH应被视为一种神经精神综合征,其表现高度可变,通过对行为、症状、癫痫后遗症和下丘脑功能障碍的全面描述能得到最佳体现。