副肿瘤性小脑变性
小脑变性
医学
脑干
恶性肿瘤
病理
共济失调
肌阵挛
小脑共济失调
视索克隆
小脑
淋巴瘤
抗体
免疫学
自身抗体
内科学
生物
神经母细胞瘤
遗传学
精神科
细胞培养
作者
Justin R. Abbatemarco,Christian A. Vedeler,John Greenlee
出处
期刊:Handbook of Clinical Neurology
日期:2024-01-01
卷期号:: 173-191
被引量:2
标识
DOI:10.1016/b978-0-12-823912-4.00030-x
摘要
Paraneoplastic cerebellar and brainstem disorders are a heterogeneous group that requires prompt recognition and treatment to help prevent irreversible neurologic injury. Paraneoplastic cerebellar degeneration is best characterized by Yo antibodies in patients with breast or ovarian cancer. Tr (DNER) antibodies in patients with Hodgkin lymphoma can also present with a pure cerebellar syndrome and is one of the few paraneoplastic syndromes found with hematological malignancy. Opsoclonus-myoclonus-ataxia syndrome presents in both pediatric and adult patients with characteristic clinical findings. Other paraneoplastic brainstem syndromes are associated with Ma2 and Hu antibodies, which can cause widespread neurologic dysfunction. The differential for these disorders is broad and also includes pharmacological side effects, infection or postinfectious processes, and neurodegenerative diseases. Although these immune-mediated disorders have been known for many years, mechanisms of pathogenesis are still unclear, and optimal treatment has not been established.
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