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神经系统副肿瘤综合征

Neurological paraneoplastic syndromes.

作者信息

Nath U, Grant R

机构信息

Department of Clinical Neurosciences, Western General Hospital, Edinburgh, UK.

出版信息

J Clin Pathol. 1997 Dec;50(12):975-80. doi: 10.1136/jcp.50.12.975.

Abstract

Paraneoplastic neurological syndromes are uncommon, however, their diagnosis is of major practical importance. The identification of antibodies in the serum or cerebrospinal fluid in central nervous system paraneoplastic syndromes confirms the clinical diagnosis of a paraneoplastic syndrome and allows early identification of an underlying tumour at a stage when it is localised and more amenable to treatment. The failure to identify antibodies in patients with characteristic presentations of underlying neurological paraneoplastic syndromes does not exclude an underlying cancer. Necrotising myelopathy, dermatomyositis, and chronic inflammatory demyelinating polyneuropathy all occur more frequently than expected in patients with cancer but autoantibodies have not yet been identified. Although significant advances have been made in diagnosis, further research is needed in the detection of autoantibodies and the elucidation of their role in the aetiology of neurological disease.

摘要

副肿瘤性神经系统综合征并不常见,然而,其诊断具有重要的实际意义。在中枢神经系统副肿瘤综合征患者的血清或脑脊液中鉴定出抗体,可确诊副肿瘤综合征,并能在肿瘤处于局限且更易于治疗的阶段早期识别出潜在肿瘤。在具有潜在神经副肿瘤综合征特征性表现的患者中未能鉴定出抗体,并不排除存在潜在癌症。坏死性脊髓病、皮肌炎和慢性炎症性脱髓鞘性多发性神经病在癌症患者中的发生率均高于预期,但尚未鉴定出自身抗体。尽管在诊断方面已取得显著进展,但在自身抗体的检测及其在神经疾病病因学中作用的阐明方面仍需进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3753/500375/17a44f97829c/jclinpath00261-0003-a.jpg

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