不恰当的笑和行为:如何,是什么,为什么?成人未确诊的弹性癫痫伴下丘脑错构瘤1例。

Nina L Beckwith, Jaclyn C Khil, Jason Teng, Kore K Liow, Alice Smith, Jesus Luna
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引用次数: 0

摘要

弹性发作(GS)是一种罕见的癫痫形式,其特征是不适当的,不受控制的笑声。它们与患者的异常认知发育和行为问题高度相关。研究表明,GS可起源于下丘脑错构瘤(HH),这是一种由灰质组成的非肿瘤性肿块,大小神经元散布着胶质核。在额叶和颞叶病变的患者中也观察到GS。本病例报告的患者是一名40岁男性,既往有脑肿瘤、糖尿病和精神分裂症病史,自8岁起每周2-3次突然无意识笑。自从这些笑声发作以来,患者表现出逐渐的认知障碍和越来越多的行为问题。随后的脑电图(21通道脑电图)显示右侧额颞区局灶性癫痫样活动,MRI研究显示下丘脑出现肿块,提示HH。其他条件应考虑在鉴别诊断笑魔和区分不同的原因可能是具有挑战性的。正如本病例报告所示,在有行为问题的患者中,特别是那些有不适当的不受控制的笑声的患者,弹性发作需要包括在鉴别诊断中。因此,彻底的检查应包括神经影像学,并注意鞍上区和脑电图。准确的早期诊断和患者教育对于避免过度和不必要的治疗至关重要。这种情况可能具有耐药性,并常伴有进行性认知和行为问题。研究表明,手术治疗方法可能有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Inappropriate Laughter and Behaviours: How, What, and Why? Case of an Adult with Undiagnosed Gelastic Seizure with Hypothalamic Hamartoma.

Inappropriate Laughter and Behaviours: How, What, and Why? Case of an Adult with Undiagnosed Gelastic Seizure with Hypothalamic Hamartoma.

Inappropriate Laughter and Behaviours: How, What, and Why? Case of an Adult with Undiagnosed Gelastic Seizure with Hypothalamic Hamartoma.

Inappropriate Laughter and Behaviours: How, What, and Why? Case of an Adult with Undiagnosed Gelastic Seizure with Hypothalamic Hamartoma.

Gelastic seizures (GS) are a rare form of epilepsy characterized by inappropriate, uncontrolled laughter. They are highly associated with abnormal cognitive development and behavioral problems in patients. Research has shown that GS can originate from hypothalamic hamartomas (HH), non- neoplastic masses consisting of gray matter with large and small neurons interspersed with glial nuclei. GS have also been observed in patients with frontal and temporal lobe lesions. The patient in this case report is a 40-year-old man with a past medical history significant for brain tumor, diabetes mellitus, and schizophrenia who presented with a long standing history of sudden, involuntary laughter occurring 2-3 times a week since 8 years old. Since the onset of these laughing spells the patient has displayed gradual cognitive impairment and increasing behavioral problems. Subsequent EEG (21-channel electroencephalogram) showed focal epileptiform activity in the right frontotemporal region and MRI studies revealed a mass arising from the hypothalamus suggestive of a HH. Other conditions should be considered in the differential diagnosis for laughing spells and distinguishing different causes can be challenging. As demonstrated by this case report, in patients with behavioral issues, especially those with inappropriate uncontrolled laughter, gelastic seizures need to be included in the differential diagnosis. Thus, a thorough workup should include neuroimaging with attention to the suprasellar region and EEG. Accurate, early diagnosis and patient education are critical in avoiding excessive and unnecessary treatments. This condition may be pharmacoresistant and is often associated with progressive cognitive and behavioral issues. Studies have shown a surgical treatment approach may be effective.

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