Schwarz J, Tatsch K, Vogl T, Kirsch C M, Trenkwalder C, Arnold G, Gasser T, Oertel W H
Department of Neurology, Klinikum Grosshadern, Ludwig-Maximilians-University, Munich, Germany.
Mov Disord. 1992;7(1):58-61. doi: 10.1002/mds.870070111.
[123I]iodobenzamide-single photon emission computed tomography (IBZM-SPECT) was employed to study the distribution of dopamine D2 receptors in a patient with biochemically proven Wilson's disease presenting with generalized dystonia. IBZM is a dopamine D2 receptor antagonist with high affinity and specific binding to basal ganglia detectable by SPECT. IBZM-SPECT in this patient (age, 20 years) displayed a striatum to frontal cortex ratio of 1.2 compared to 1.55 +/- 0.05 (mean +/- SD) in normal controls (n = 7; mean age, 53.3 years). In parallel with this finding, MRI with heavily T2-weighted sequences showed atrophy and low signal intensity changes of the basal ganglia. There was no improvement of dystonia after a subcutaneous injection of apomorphine. In contrast, IBZM-SPECT of a neurologically asymptomatic Wilson's disease patient (age, 21 years) displayed a striatum to frontal cortex ratio of 1.6. The MRI scan of this patient was normal. It is suggested that the observed apomorphine-unresponsive generalized dystonia in this Wilson's disease patient is related to striatal lesions proven by IBZM-SPECT and MRI.
采用[123I]碘苯甲酰胺单光子发射计算机断层扫描(IBZM-SPECT)研究一名经生化证实患有威尔逊病且表现为全身性肌张力障碍患者的多巴胺D2受体分布情况。IBZM是一种多巴胺D2受体拮抗剂,对基底神经节具有高亲和力且能被SPECT检测到特异性结合。该患者(20岁)的IBZM-SPECT显示纹状体与额叶皮质的比值为1.2,而正常对照组(n = 7;平均年龄53.3岁)的该比值为1.55±0.05(平均值±标准差)。与此发现相一致的是,采用重T2加权序列的MRI显示基底神经节萎缩及低信号强度改变。皮下注射阿扑吗啡后肌张力障碍无改善。相比之下,一名神经学上无症状的威尔逊病患者(21岁)的IBZM-SPECT显示纹状体与额叶皮质的比值为1.6。该患者的MRI扫描结果正常。提示在这名威尔逊病患者中观察到的对阿扑吗啡无反应的全身性肌张力障碍与IBZM-SPECT和MRI证实的纹状体病变有关。