Urban P P, Wicht S, Vukurevic G, Fitzek C, Fitzek S, Stoeter P, Massinger C, Hopf H C
Department of Neurology, Institute of Neuroradiology, University of Mainz, Germany.
Neurology. 2001 Apr 24;56(8):1021-7. doi: 10.1212/wnl.56.8.1021.
Although dysarthria is a frequent symptom in cerebral ischemia, there is little information on its anatomic specificity, spectrum of associated clinical characteristics, and etiologic mechanisms.
An investigation of 68 consecutive patients with sudden onset of dysarthria due to a single infarction confirmed by MRI or CT was conducted.
Dysarthria was associated with a classic lacunar stroke syndrome in 52.9% of patients. Isolated dysarthria and dysarthria-central facial and lingual paresis occurred in 2.9% (n = 2) and 10.3% (n = 7), respectively. Dysarthria-clumsy hand syndrome was observed in 11.7% (n = 8) of patients and associated with pure motor hemiparesis and/or ataxic hemiparesis in 27.9% (n = 19). The lesions were due to small-vessel disease in 52.9% (n = 36), to cardioembolism in 11.8% (n = 8), and to large-vessel disease in only 4.4% (n = 3) of cases. Infarctions were located in the lower part of the primary motor cortex (5.9%; n = 4), middle part of the centrum semiovale (23.5%; n = 16), genu and ventral part of the dorsal segment of the internal capsule (8.8%; n = 6), cerebral peduncle (1.5%; n = 1), base of the pons (30.9%; n = 21), and ventral pontomedullary junction (1.5%; n = 1). Isolated cerebellar infarctions affected the rostral paravermal region in the superior cerebellar artery territory.
Extracerebellar infarcts causing dysarthria were located in all patients along the course of the pyramidal tract. This finding correlates with the frequent occurrence of associated pyramidal tract signs in 90.7% (n = 62) of patients. Isolated cerebellar infarcts leading to dysarthria were in all cases located in the territory of the superior cerebellar artery.
尽管构音障碍是脑缺血的常见症状,但关于其解剖学特异性、相关临床特征谱及病因机制的信息却很少。
对68例经MRI或CT证实因单一梗死导致突然出现构音障碍的连续患者进行了调查。
52.9%的患者构音障碍与典型的腔隙性卒中综合征相关。孤立性构音障碍以及构音障碍合并中枢性面舌瘫分别出现在2.9%(n = 2)和10.3%(n = 7)的患者中。11.7%(n = 8)的患者出现构音障碍-笨拙手综合征,其中27.9%(n = 19)与纯运动性偏瘫和/或共济失调性偏瘫相关。52.9%(n = 36)的病例病变归因于小血管疾病,11.8%(n = 8)归因于心源性栓塞,仅4.4%(n = 3)的病例归因于大血管疾病。梗死位于初级运动皮层下部(5.9%;n = 4)、半卵圆中心中部(23.5%;n = 16)、内囊后肢膝部和腹侧部(8.8%;n = 6)、大脑脚(1.5%;n = 1)、脑桥基底部(30.9%;n = 21)以及脑桥延髓腹侧交界处(1.5%;n = 1)。孤立性小脑梗死累及小脑上动脉供血区的嘴侧旁中央区域。
所有导致构音障碍的小脑外梗死均位于锥体束走行部位。这一发现与90.7%(n = 62)的患者频繁出现相关锥体束征相符。所有导致构音障碍的孤立性小脑梗死均位于小脑上动脉供血区。