Sakakibara R, Hattori T, Tojo M, Yamanishi T, Yasuda K, Hirayama K
Department of Neurology, Chiba University School of Medicine, Japan.
Jpn J Psychiatry Neurol. 1993 Sep;47(3):591-8. doi: 10.1111/j.1440-1819.1993.tb01804.x.
Detailed micturitional histories and urodynamic studies were conducted to investigate the micturitional disturbance in multiple system atrophy (MSA). Eighty-six patients with MSA comprised of 14 with striatonigral degeneration (SND), 42 with olivopontocerebellar atrophy (OPCA) and 30 with Shy-Drager syndrome (SDS). The results were as follows. Micturitional symptoms were noted in over 90% of patients with each type of MSA. Dominant symptoms were irritative ones in SND and OPCA, and a combination of irritative and obstructive ones in SDS. Micturitional symptoms in SDS appeared earlier than those in SND or OPCA. The degree of micturitional disturbance was severer in SDS than in SND or OPCA. Micturitional disturbance tended to become worse as the disease progressed. The responsible sites of lesions of micturitional disturbance seemed to be supra- as well as infranuclear lesions of the pelvic and pudendal nerves in MSA. Infranuclear lesions were more prominent in SDS than in SND or OPCA. Follow-up studies of some of the patients with SDS and OPCA suggested that the responsible sites of pelvic nerve lesions changed from supra- to infranuclear lesions during the course of disease.
为研究多系统萎缩(MSA)患者的排尿障碍,我们进行了详细的排尿史调查和尿动力学研究。86例MSA患者包括14例纹状体黑质变性(SND)、42例橄榄脑桥小脑萎缩(OPCA)和30例Shy-Drager综合征(SDS)。结果如下:各类MSA患者中超过90%出现排尿症状。SND和OPCA的主要症状为刺激性症状,而SDS的症状为刺激性和梗阻性症状的组合。SDS患者的排尿症状比SND或OPCA患者出现得更早。SDS患者排尿障碍的程度比SND或OPCA患者更严重。排尿障碍往往随着疾病进展而加重。MSA患者排尿障碍的病变责任部位似乎是盆腔神经和阴部神经的核上及核下病变。SDS患者的核下病变比SND或OPCA患者更突出。对部分SDS和OPCA患者的随访研究表明,盆腔神经病变的责任部位在疾病过程中从核上病变转变为核下病变。