在一个老年男性中非解决的,渐进的,非基性高血糖症 Hemichorea-Hemiballismus 综合征
Akash Chandani1, Cyrine Cunanan1, Sumathi Krishnan2
1Internal Medicine, North Middlesex University Hospital, London, GBR.
Cureus
|November 17, 2025
概括
非基性高血糖性 Hemichorea-hemiballismus 综合征是一种与不受控制的糖尿病相关的罕见神经疾病,可以导致非自愿的运动. 有效的管理包括控制血糖和使用神经乱治疗来缓解症状.
科学领域:
- 神经学 神经学
- 内分泌学 在内分泌学.
- 代谢障碍 代谢障碍 代谢障碍
背景情况:
- 非基性高血糖性 Hemichorea-hemiballismus 综合征是一种罕见的神经疾病.
- 它与不受控制的糖尿病糖尿病引起的高血糖症有关.
研究的目的:
- 介绍一个患有T2DM的老年男性患者的病例,该患者患有 Hemichorea-hemiballismus.
- 强调考虑老年人这些运动障碍的代谢原因的重要性.
主要方法:
- 一个80多岁的男性患有T2DM的病例介绍.
- 临床评估包括神经学检查和脑部成像 (CT扫描).
- 管理重点是血糖控制和神经乱药物治疗.
主要成果:
- 患者在身体左侧呈现出渐进的非自愿运动.
- 图像显示右基底质的高密度,与该综合征一致.
- 症状随着改善的血糖控制和神经乱药治疗而消失.
结论:
- 在老年患者中,应考虑代谢原因,特别是糖尿病中高血糖症,患有血糖-血球.
- 血糖控制对于管理这种综合症和改善患者的生活质量至关重要.
相关概念视频
Hyperglycemia
34
Hyperglycemia is an abnormally high blood glucose level. It is diagnosed by fasting glucose ≥126 mg/dL, 2-hour oral glucose tolerance test (or OGTT) ≥200 mg/dL, random glucose ≥200 mg/dL with symptoms, or HbA1c ≥6.5%. However, HbA1c results may be unreliable in certain conditions, such as anemia or hemoglobinopathies, and the diagnosis should be confirmed unless classic symptoms are present. Postprandial hyperglycemia is typically considered significant when glucose...
34
Hyperosmolar Hyperglycemic State
28
Hyperosmolar Hyperglycemic State, or HHS, is a serious and life-threatening complication of type 2 diabetes mellitus. It is characterized by three main features: severe hyperglycemia, profound dehydration, and elevated serum osmolality, all occurring without significant ketoacidosis.HHS typically develops in older adults or individuals with limited access to fluids. This may result from illness, cognitive impairment, or medications such as diuretics or corticosteroids. These factors reduce...
28
Alzheimer Disease l: Introduction
29
Alzheimer disease is a chronic, progressive, and irreversible neurodegenerative disorder and the most common cause of dementia in older adults. It leads to gradual neuronal loss, causing cognitive decline, behavioral changes, and loss of functional independence.Risk Factors and EtiologyThe disease is multifactorial. Age is the strongest risk factor, with prevalence doubling every 5 years after age 65. Genetic factors include mutations in genes such as APP, PSEN1, and PSEN2, which are associated...
29
Huntington Disease l: Introduction
166
Huntington disease or HD is a progressive, fatal neurodegenerative disorder inherited in an autosomal dominant pattern.PathophysiologyIt is caused by expansion of the CAG trinucleotide repeat in the HTT gene on chromosome 4 (4p16.3), producing an abnormal huntingtin protein with an expanded polyglutamine tract. This misfolded protein disrupts cellular function, leading to neuronal death. Normal alleles have ≤26 repeats, 27–35 are intermediate (risk of expansion), 36–39 show...
166
Dementia l: Introduction
35
Dementia is an acquired, progressive syndrome characterized by a decline in multiple cognitive domains severe enough to impair daily functioning and reduce independence. Although memory loss is a central feature, the diagnosis requires additional deficits involving language, executive function, visuospatial skills, judgment, calculation, or abstract reasoning. These cognitive impairments reflect underlying neurodegenerative or vascular processes that gradually disrupt neuronal networks...
35
Hepatic Encephalopathy
71
DefinitionHepatic encephalopathy is a reversible neurologic syndrome that results from advanced liver dysfunction or portosystemic shunting. It leads to disturbances in cognition, behavior, and motor function due to the brain’s exposure to gut-derived toxins that the liver fails to detoxify.EtiologyThis condition develops either in the setting of acute fulminant hepatitis or progressively during chronic liver disease, such as cirrhosis and portal hypertension. Portosystemic...
71


