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Cysticercosis--review of 230 patients. 囊虫病——230例病例回顾
Pub Date : 1985-01-01
G F McCormick

Two hundred thirty patients with cysticercosis were reviewed. Investigation with CT scan has led to a more detailed understanding of the natural history of human infestation which is essential to the evaluation of new pharmacological and neurosurgical treatments. In contrast to reports emphasizing the need to extirpate all intraventricular cysts, many of our patients needed only ventricular shunt implantation. The ability to evaluate and reevaluate hydrocephalus by CT scan permitted comfortable use of ventricular shunt insertion as the only treatment. Nevertheless, cysts in the fourth ventricle should nearly always be extirpated, because these cysts, by their mass effect, may cause herniation even after shunt implantation. Serious morbidity and death occur chiefly in patients who develop hydrocephalus from intraventricular and basilar infestation. It is unlikely that praziquantel will be effective in patients who present with symptoms of hydrocephalus.

本文回顾了230例囊虫病患者。CT扫描的研究使我们对人类感染的自然历史有了更详细的了解,这对评估新的药理学和神经外科治疗方法至关重要。与强调需要切除所有脑室内囊肿的报道相反,我们的许多患者只需要脑室分流植入。通过CT扫描评估和重新评估脑积水的能力允许舒适地使用脑室分流术作为唯一的治疗方法。然而,第四脑室的囊肿几乎总是应该切除,因为这些囊肿,由于它们的质量效应,即使在分流器植入后也可能引起疝。严重的发病率和死亡主要发生在脑室内和基底部感染的脑积水患者中。吡喹酮不太可能对出现脑积水症状的患者有效。
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引用次数: 0
Neuromuscular transmission defect in inherited polyneuropathy. 遗传性多发性神经病的神经肌肉传递缺陷。
Pub Date : 1985-01-01
J J Kelly, G A Baquis, L S Adelman, T L Munsat

A 51-year-old woman with an inherited polyneuropathy had fatiguability and a dramatic historical response to prostigmine. Repetitive motor nerve stimulation produced a prominent decrement of the compound muscle action potential in distal muscles with marked facilitation after brief exercise. Defective neuromuscular transmission paralleled the polyneuropathy in distribution and severity. We hypothesize that deficient release of acetylcholine by regenerating or degenerating nerve terminals likely caused the defect of neuromuscular transmission in this patient.

51岁女性,遗传性多神经病变,易疲劳,对前体素有明显的历史反应。重复性运动神经刺激使远端肌肉复合动作电位明显下降,且在短暂运动后易化。神经肌肉传导缺陷在分布和严重程度上与多发性神经病相似。我们推测,再生或退行性神经末梢导致乙酰胆碱释放不足可能导致该患者神经肌肉传递缺陷。
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引用次数: 0
Somatostatin in cerebrospinal fluid. 脑脊液中的生长抑素
Pub Date : 1985-01-01
P E Cooper
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引用次数: 0
Some problems associated with neuropsychological assessment. 一些与神经心理学评估有关的问题。
Pub Date : 1985-01-01
A Benton
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引用次数: 0
HLA and complement studies in Alzheimer's disease. HLA和补体在阿尔茨海默病中的研究。
Pub Date : 1985-01-01
C M Hulette, R L Walford
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引用次数: 0
Brain biopsy in Alzheimer's disease: surgical technique and indications. 阿尔茨海默病的脑活检:手术技术和适应症。
Pub Date : 1985-01-01
R E Harbaugh
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引用次数: 0
A new model of focal cerebral ischemia: validation and utility. 一种新的局灶性脑缺血模型:验证与应用。
Pub Date : 1985-01-01
P D Lyden, J Seelig, R P Martin, S Yoshida, M Bailey, J F Rothrock, J A Alksne
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引用次数: 0
Heterogeneity and prognosis in dementia of the Alzheimer type. 阿尔茨海默型痴呆的异质性和预后。
Pub Date : 1985-01-01 DOI: 10.7916/D8ZS4CZ8
R. Mayeux, Y. Stern, M. Sano
The diagnosis of dementia of the Alzheimer type (DAT) depends on the clinician's ability to document intellectual impainnent in the patient and to exclude other causes of dementia. About 50% of all demented patients entering a hospital are ultimately found at postmortem examination to have Alzheimer's disease. However, using the most rigorous criteria the accuracy of correct clinical diagnosis at autopsy approaches only 80-90% and this excludes some unusual patients. Most investigators use the Diagnostic and Statistical Manual of Mental Disorder-third ed. (DSM-III) criteria for dementia, a rating of perfonnance in activities of daily living, and an assessment of personality and intellectual function for diagnosis. Two clinical rating scales: the Blessed Dementia Rating Scale (parts 1 and 2) and the Clinical Dementia Rating Scale, are used frequently and seem to identify patients with DAT with greater accuracy than other scales. Our assessment protocol for dementia includes a quantitative neurological examination because certain motor manifestations have been observed in DAT: myoclonus, rigidity, stooped posture, and bradykinesia. We found these clinical features to be useful in predicting the course in some patients. Our data indicate clinical heterogeneity in DAT and may suggest the presence of unique subgroups.
阿尔茨海默型痴呆(DAT)的诊断取决于临床医生记录患者智力损伤的能力,并排除痴呆的其他原因。入院的所有痴呆患者中,约有50%最终在尸检时被发现患有阿尔茨海默病。然而,使用最严格的标准,正确的临床诊断的准确性在尸检接近只有80-90%,这排除了一些不寻常的病人。大多数研究者使用第三版《精神障碍诊断与统计手册》(DSM-III)的痴呆标准,对日常生活活动的表现进行评估,并对人格和智力功能进行评估。两种临床评定量表:祝福痴呆评定量表(第1部分和第2部分)和临床痴呆评定量表被频繁使用,似乎比其他量表更准确地识别出患有DAT的患者。我们对痴呆的评估方案包括定量的神经学检查,因为在DAT中观察到某些运动表现:肌阵挛、僵硬、弯腰和运动迟缓。我们发现这些临床特征对预测某些患者的病程是有用的。我们的数据显示了DAT的临床异质性,可能表明存在独特的亚群。
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引用次数: 7
Workshop on early diagnosis in Alzheimer's disease. November 6-7, 1985. 阿尔茨海默病早期诊断研讨会。1985年11月6日至7日。
Pub Date : 1985-01-01
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引用次数: 0
Cerebral biopsy in the study of Alzheimer's disease. 阿尔茨海默病的脑活检研究。
Pub Date : 1985-01-01
D M Bowen, D Neary
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引用次数: 0
期刊
Bulletin of clinical neurosciences
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