Neurology Service, George E. Wahlen Veterans Affairs Medical Center, Salt Lake City, UT 84148, USA.
J Neurol Sci. 2010 Apr 15;291(1-2):74-8. doi: 10.1016/j.jns.2009.12.019. Epub 2010 Jan 20.
Paraneoplastic neurological syndromes are unusual in prostatic cancer, and paraneoplastic cerebellar degeneration associated with adenocarcinoma of the prostate is rare. Here we report a 68year old man who developed progressive ataxia in the setting of stage D2 adenocarcinoma of the prostate and whose MRI showed cerebellar atrophy. The patient's serum produced a previously undescribed pattern of immunoreactivity, binding to nuclei and cytoplasm of Purkinje cells, deep cerebellar neurons, scattered cells in the molecular and granule cell layers, and neuronal populations in thalamus, cerebral cortex, and hippocampus but not with liver or kidney. The patient's IgG also labeled a 65kDa protein, discrete from Yo antigen, in Western blots of Purkinje cell lysates and did not react with blotted recombinant HuD, Ri, Yo, or amphiphysin proteins. Sera from neurologically normal patients with adenocarcinoma of the prostate did not contain this antibody, and the patient's serum did not react with normal prostate or with prostatic adenocarcinomas from other individuals. Prostatic adenocarcinoma may occasionally be accompanied by development of anticerebellar antibodies. Adenocarcinoma of the prostate should be considered as a possible underlying malignancy in older males with unexplained progressive cerebellar degeneration.
副肿瘤性神经系统综合征在前列腺癌中不常见,与前列腺腺癌相关的副肿瘤性小脑变性则更为罕见。本文报告了一例 68 岁男性,患有 D2 期前列腺腺癌,出现进行性小脑共济失调,MRI 显示小脑萎缩。患者的血清产生了一种以前未描述的免疫反应模式,与浦肯野细胞、深部小脑神经元、分子层和颗粒细胞层中的散在细胞以及丘脑、大脑皮层和海马中的神经元群的细胞核和细胞质结合,但不与肝或肾结合。患者的 IgG 还标记了浦肯野细胞裂解物 Western 印迹中与 Yo 抗原分离的 65kDa 蛋白,并且不与印迹的重组 HuD、Ri、Yo 或 amphiphysin 蛋白反应。来自患有前列腺腺癌的神经正常患者的血清不含有这种抗体,并且患者的血清也不与正常前列腺或来自其他个体的前列腺腺癌反应。前列腺腺癌偶尔可能伴有抗小脑抗体的产生。对于不明原因进行性小脑变性的老年男性,前列腺腺癌应被视为潜在的恶性肿瘤。