Dalmau J O, Posner J B
Department of Neurology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Arch Neurol. 1999 Apr;56(4):405-8. doi: 10.1001/archneur.56.4.405.
The fact that a small cancer hidden in the chest, abdomen, or pelvis could destroy or damage portions of the nervous system, such as cerebellar Purkinje cells or cholinergic synapses, has intrigued neurologists since paraneoplastic syndromes were first described. In 1965, when little was known about their pathogenesis, a full issue of the journal Brain and an international symposium were devoted to paraneoplastic disorders. In this decade, the discovery of several paraneoplastic antibodies that react with both the nervous system and the causal cancer has rekindled interest in these syndromes (Table). Several other factors make these rare syndromes of clinical and scientific interest. A recent review by Dalmau and Posner contains a more comprehensive bibliography of paraneoplastic syndromes.
自副肿瘤综合征首次被描述以来,隐藏在胸部、腹部或骨盆中的小肿瘤能够破坏或损伤神经系统的某些部分,如小脑浦肯野细胞或胆碱能突触,这一事实一直吸引着神经学家。1965年,当人们对其发病机制知之甚少时,《大脑》杂志的一整期以及一次国际研讨会都专门讨论了副肿瘤性疾病。在这十年里,几种能与神经系统和引发癌症的肿瘤发生反应的副肿瘤抗体的发现,重新激发了人们对这些综合征的兴趣(见表)。还有其他几个因素使得这些罕见综合征具有临床和科学研究价值。达尔毛和波斯纳最近的一篇综述包含了更全面的副肿瘤综合征参考文献。