Anti-NMDAR-Positive Small-Cell Lung Cancer Paraneoplastic Limbic Encephalitis: A Case Report and Literature Review.

IF 0.9 Q4 CLINICAL NEUROLOGY Case Reports in Neurological Medicine Pub Date : 2020-06-02 eCollection Date: 2020-01-01 DOI:10.1155/2020/5269352
Raman Sohal, Steven H Adams, Vishal Phogat, Abha Harish, Carlos Ynigo D Lopez, Michael P A Williams, Kamal K Khurana, Basel Abuzuaiter, Nia Jagroop, Bhavya Narapureddy
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Abstract

Introduction: Paraneoplastic limbic encephalitis (PLE) is a rare disease that presents as rapid onset dementia characterized by short-term memory loss (STM), anxiety, and behavioral changes. Anti-NMDAR antibodies are unfrequently reported in PLE associated with small-cell lung cancer (SCLC). Given that PLE can precede the diagnosis of cancer, it is very important that once infectious, metabolic, nutritional, or structural disorders associated with short-term memory loss are ruled out that vigorous effort must be made to rule out underlying malignancy.

Case: We report a rare case of PLE as the presenting symptom of SCLC. A 72-year-old male with history of COPD was brought to the ED by his wife after he was found to have short-term memory loss, including forgetfulness of his wedding anniversary the day before, and anxiety. Neurological exam showed impaired short-term recall on MOCA. CT head showed no evidence of infarct. Lumbar puncture was performed which showed lymphocytic pleocytosis, a nonspecific inflammatory change. CSF panel was negative for HSV, Neisseria, Hemophilus, E. coli, and HIV. Initial EEG was unremarkable, though a repeat EEG showed mild slowing of the posterior dominant rhythm consistent with mild encephalopathy. MRI showed equivocal increased FLAIR on T2-weighted images in the bilateral temporal lobes, left greater than right. CTA thorax showed bulky mediastinal and right hilar LAD. FNA of the R4 lymph node revealed SCLC. The NM bone scan showed no osteoblastic lesions. While the serum autoantibody panel was positive for anti-NMDAR, the CSF autoantibody panel returned entirely negative. Chemotherapy with etoposide and cisplatin was started on Day 4 of admission. The patient's neurological symptoms showed improvement following chemotherapy.

Conclusion: This case highlights the importance of recognizing short-term memory loss as a feature of PLE.

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抗nmdar阳性小细胞肺癌副肿瘤边缘脑炎1例并文献复习。
简介:副肿瘤边缘脑炎(PLE)是一种罕见的疾病,表现为以短期记忆丧失(STM)、焦虑和行为改变为特征的快速发作性痴呆。抗nmdar抗体在与小细胞肺癌(SCLC)相关的PLE中很少报道。鉴于PLE可以先于癌症的诊断,一旦排除了与短期记忆丧失相关的感染性、代谢性、营养性或结构性疾病,就必须大力排除潜在的恶性肿瘤,这一点非常重要。病例:我们报告一例罕见的以小细胞肺癌为主要症状的原发性脑出血病例。一位有慢性阻塞性肺病病史的72岁男性被妻子带到急诊科,因为他被发现有短期记忆丧失,包括忘记前一天结婚纪念日和焦虑。神经学检查显示MOCA短期记忆受损。头部CT未见梗死灶。腰椎穿刺显示淋巴细胞增多症,一种非特异性炎症改变。脑脊液面板阴性HSV,奈瑟氏菌,血友病,大肠杆菌和艾滋病毒。初始脑电图无明显异常,但重复脑电图显示轻度后优势节律减慢,符合轻度脑病。MRI显示双侧颞叶t2加权FLAIR模糊增加,左侧大于右侧。CTA胸廓显示纵隔和右门LAD肿大。R4淋巴结FNA显示SCLC。NM骨扫描未见成骨细胞病变。血清自身抗体组抗nmdar阳性,脑脊液自身抗体组完全阴性。入院第4天开始依托泊苷联合顺铂化疗。化疗后病人的神经症状有所改善。结论:本病例强调了将短期记忆丧失视为PLE特征的重要性。
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