Buchholz D W
Johns Hopkins University School of Medicine, Baltimore, Maryland 21287-0876.
Dysphagia. 1994 Fall;9(4):245-55. doi: 10.1007/BF00301918.
The potential causes of neurogenic oropharyngeal dysphagia in cases in which the underlying neurologic disorder is not readily apparent are discussed. The most common basis for unexplained neurogenic dysphagia may be cerebrovascular disease in the form of either confluent periventricular infarcts or small, discrete brainstem stroke, which may be invisible by magnetic resonance imaging. The diagnosis of occult stroke causing pharyngeal dysphagia should not be overlooked, because this diagnosis carries important treatment implications. Motor neuron disease producing bulbar palsy, pseudobulbar palsy, or a combination of the two can present as gradually progressive dysphagia and dysarthria with little if any limb involvement. Myopathies, especially polymyositis, and myasthenia gravis are potentially treatable disorders that must be considered. A variety of medications may cause or exacerbate neurogenic dysphagia. Psychiatric disorders can masquerade as swallowing apraxia. The basis for unexplained neurogenic dysphagia can best be elucidated by methodical evaluation including careful history, neurologic examination, videofluoroscopy of swallowing, blood studies (CBC, chemistry panel, creatine kinase, B12, thyroid screening, and anti-acetylcholine receptor antibodies), electromyography, and magnetic resonance imaging (MRI) of the brain, plus additional procedures such as lumbar puncture and muscle biopsy as indicated. Little is known about aging and neurogenic dysphagia, specifically the relative contributions of natural age-related changes in the oropharynx and of diseases of the elderly, including periventricular MRI abnormalities, in producing dysphagia symptoms and videofluoroscopic abnormalities in this population.
本文讨论了潜在神经疾病不明显的神经源性口咽吞咽困难的可能病因。不明原因的神经源性吞咽困难最常见的原因可能是脑血管疾病,表现为融合性脑室周围梗死或小的、散在的脑干卒中,磁共振成像可能无法显示这些病变。隐匿性卒中导致咽吞咽困难的诊断不应被忽视,因为这一诊断具有重要的治疗意义。运动神经元病导致的球麻痹、假性球麻痹或两者合并,可表现为逐渐进展的吞咽困难和构音障碍,且很少或几乎没有肢体受累。肌病,尤其是多发性肌炎和重症肌无力,是必须考虑的潜在可治疗疾病。多种药物可能导致或加重神经源性吞咽困难。精神疾病可伪装成吞咽失用症。不明原因的神经源性吞咽困难的病因最好通过系统评估来阐明,包括详细的病史、神经系统检查、吞咽视频透视检查、血液检查(血常规、生化指标、肌酸激酶、维生素B12、甲状腺筛查和抗乙酰胆碱受体抗体)、肌电图、脑部磁共振成像(MRI),以及根据需要进行的其他检查,如腰椎穿刺和肌肉活检。关于衰老与神经源性吞咽困难,尤其是口咽自然年龄相关变化和老年人疾病(包括脑室周围MRI异常)在该人群中导致吞咽困难症状和吞咽视频透视异常方面的相对作用,目前知之甚少。