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非霍奇金淋巴瘤患者中伴慢性炎性脱髓鞘性多发性神经病的抗Ma2相关边缘叶脑炎:一例报告

Anti-Ma2-associated limbic encephalitis with coexisting chronic inflammatory demyelinating polyneuropathy in a patient with non-Hodgkin lymphoma: A case report.

作者信息

Ju Weina, Qi Baochang, Wang Xu, Yang Yu

机构信息

Department of Neurology Department of Orthopedic Trauma, the First Hospital of Jilin University, Changchun, Jilin, China.

出版信息

Medicine (Baltimore). 2017 Oct;96(40):e8228. doi: 10.1097/MD.0000000000008228.

Abstract

RATIONALE

We report the rare case of a 74-year-old man with anti-Ma2-associated paraneoplastic neurologic syndrome (PNS), and review and analyze the clinical manifestations, diagnosis, and treatment of the disease.

PATIENT CONCERNS

The patient presented with a 5-month history of muscle weakness, progressive body aches, and weakness and numbness in both lower extremities. Before his hospitalization, he had experienced cognitive function decline; ptosis, inward gaze, and vertical gaze palsy in the right eye; and occasional visual hallucinations. Brain and spinal cord magnetic resonance imaging (MRI) yielded normal results. Anti-Ma2 antibodies were detected in both serum and cerebrospinal fluid. A 4-hour electroencephalogram showed irregular sharp slow waves and δ waves in the temporal region. Electromyography showed peripheral nerve demyelination. Positron-emission tomography/computed tomography (PET-CT) examination revealed hypermetabolism in the lymph nodes of the whole body. Biopsy of the lymph nodes showed non-Hodgkin lymphoma.

DIAGNOSIS

A clinical diagnosis of lymphoma and PNS was made.

INTERVENTIONS

The patient was treated with intravenous dexamethasone (15 mg/day) for 3 days.

LESSONS

We have presented a rare case of a PNS involving both the central and peripheral nervous systems. The clinical features of this case indicated anti-Ma2-associated encephalitis and chronic inflammatory demyelinating polyneuropathy. PET-CT played a critical role in enabling early diagnosis and prompt treatment in this case.

摘要

原理

我们报告了一例罕见的74岁男性抗Ma2相关副肿瘤性神经综合征(PNS)病例,并对该疾病的临床表现、诊断和治疗进行回顾与分析。

患者情况

该患者有5个月的肌肉无力、进行性全身疼痛以及双下肢无力和麻木病史。住院前,他出现认知功能下降;右眼上睑下垂、内斜视和垂直凝视麻痹;以及偶尔的视幻觉。脑和脊髓磁共振成像(MRI)结果正常。血清和脑脊液中均检测到抗Ma2抗体。4小时脑电图显示颞区有不规则尖慢波和δ波。肌电图显示周围神经脱髓鞘。正电子发射断层扫描/计算机断层扫描(PET-CT)检查显示全身淋巴结代谢增高。淋巴结活检显示为非霍奇金淋巴瘤。

诊断

临床诊断为淋巴瘤和PNS。

干预措施

患者接受静脉注射地塞米松(15毫克/天)治疗3天。

经验教训

我们展示了一例罕见的累及中枢和周围神经系统的PNS病例。该病例的临床特征提示为抗Ma2相关脑炎和慢性炎症性脱髓鞘性多发性神经病。PET-CT在该病例的早期诊断和及时治疗中发挥了关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a8f/5738013/60abdf77b945/medi-96-e8228-g001.jpg

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