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OPCA的MRI影像诊断与临床

MRI diagnosis and clinical manifestation of OPCA
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摘要 目的:探讨OPCA的MRI征象,及与临床表现的关系。方法:回顾性分析30例OPCA的MRI影像学表现。结果:根据MRI征象将OPCA分为轻、中和重度3度。本组轻度者5例,中度者8例,重度者7例。轻度者:小脑脑沟增多、加深,脑干略变细,桥脑无明显改变。中度者:除前者征象外,可见桥脑腹侧萎缩,四脑室扩大,脑干周围基底池扩大。重度者:小脑、桥脑腹侧,延髓橄榄重度萎缩,小脑核,桥脑被盖,小脑下部不受累。临床症状以小脑性共济失调为主且是首发症状,占23例(76.6%),双下肢乏力4例(13.6%),帕金森氏综合征2例(9.4%);精神异常1例(3.4%),其它症状共占16.2%(包括闪电样疼痛,括约肌障碍,吞咽困难,视力减退,精神运动退变等)。结论:MRI可清楚显示 OPCA的病变程度,T1W像矢状位显示最佳,临床表现与 MRI所示病变程度密切相关。 Objective To study the MRI signs of OPCA and the relationship with clinical manifestion.Methods:30 cases of MRI manifestion of OPCA were reviewed retorseperctively. Results: According to the MRI signs, these 30 cases were divided into 3 types, mild degree 5 cases,moderate degree cases indicated that their cerebellar fold increased and deepened, brain stem slightly became thin, pontine had no clearly atrophy.To the mod- erate ones, except having all the signs of the mild ones,they showed that their pontine internal side atrophied ,four encephalocoeles,brain stem basi- laris pool dilated,the severe ones indicated that cerebell,pointine internal side and bulbaroliver seriously atrophied. According to the clinical observa- tion,the clinical manifestation mainly indicated cerebellarataxia, and 23 cases (76.6%) presented primary symptom, 4 cases (13.6%) presented two lower limbs fatigued,2 cases (9.4%)appeared Pakinsonian syndrome and 1 cases (3.4%)presented mental disorders. There are another symptom (16.2% ) (such as glistening ache,language disorders,swallow distress,eyesight weakened,mental movement degeneration and so on). Conclusion: MBI could clearly indicate the pathological changes degree of OPCA T1 W sagittal sections indication os excellent. Clinical manifestion has close rela- tionship with the pathological changes degree that MRI indicated.
出处 《河南实用神经疾病杂志》 2000年第5期5-6,共2页 Henan Journal of Practical Nervous Diseases
关键词 遗传性共济失调 诊断 MRI OPCA Olivoponto cerebeller atrophy(OPCA) Magnetic resonance image Diagnosis
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  • 1Y. Kageyama,K. Ichikawa,A. Fujioka,A. Tsutsumi,S. Yorifuji,K. Miyoshi. An autopsy case of mitochondrial encephalomyopathy with prominent degeneration in olivo-ponto-cerebellar system[J] 1991,Acta Neuropathologica(1):99~103

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