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病例报告:一例转移性脑肿瘤和癌性脑膜炎酷似副肿瘤性神经综合征患者的尸检报告。

Case report: An autopsy report of patient with metastatic brain tumor and carcinomatous meningitis mimicking paraneoplastic neurological syndrome.

作者信息

Amano Ryota, Sunouchi Azusa, Yokota Yuka, Mochizuki Kunio

机构信息

Department of Neurology, Fujiyoshida Municipal Medical Center, Yamanashi, Japan.

Department of Pathology, University of Yamanashi, Yamanashi, Japan.

出版信息

Front Neurol. 2024 Oct 11;15:1471668. doi: 10.3389/fneur.2024.1471668. eCollection 2024.

Abstract

Differential diagnosis of metastatic brain tumor, carcinomatous meningitis, and paraneoplastic neurological syndrome (PNS) can be challenging in atypical cases. When examining patient with increased T2 fluid-attenuated inversion recovery (FLAIR) hyperintensities in the temporal polar white matter, autoimmune encephalitis, including PNS, should be considered. Herein, we report the case of an 85-year-old man with carcinomatous meningitis due to lung large cell carcinoma. He showed disturbance of consciousness, abnormal behavior, incomprehensible speech, and apathy, which suggested brain dysfunction. Magnetic resonance imaging revealed high intensities on the whole cerebellum on a diffusion-weighted image and bilateral T2 FLAIR hyperintensities in the temporal polar white matter. Cerebrospinal fluid analysis and cytology showed elevated total protein levels, pleocytosis, and atypical cells with nuclear enlargement, hyperchromasia, and irregular shape. Autopsy revealed lung large cell carcinoma and its brain metastasis. Tumor cells were disseminated to the central nervous system along the subarachnoid space. Furthermore, plenty of carcinoma cells and peritumoral enlarged perivascular space were observed in the temporal poles. To our knowledge, this is the first report of bilateral T2 FLAIR hyperintensities in the temporal polar white matter caused by carcinomatous meningitis with pathological confirmation. In patient with carcinomatous meningitis, abnormal T2 FLAIR hyperintensities may not be derived from ischemia or tumor invasion to parenchyma.

摘要

在非典型病例中,转移性脑肿瘤、癌性脑膜炎和副肿瘤性神经系统综合征(PNS)的鉴别诊断可能具有挑战性。当检查颞极白质T2液体衰减反转恢复(FLAIR)高信号增强的患者时,应考虑自身免疫性脑炎,包括PNS。在此,我们报告一例85岁因肺大细胞癌导致癌性脑膜炎的男性病例。他表现出意识障碍、行为异常、言语不清和淡漠,提示脑功能障碍。磁共振成像显示在扩散加权图像上整个小脑呈高信号,在颞极白质有双侧T2 FLAIR高信号。脑脊液分析和细胞学检查显示总蛋白水平升高、细胞增多以及具有核增大、核染色质增多和形状不规则的非典型细胞。尸检发现肺大细胞癌及其脑转移。肿瘤细胞沿蛛网膜下腔扩散至中枢神经系统。此外,在颞极观察到大量癌细胞和肿瘤周围扩大的血管周围间隙。据我们所知,这是首例经病理证实由癌性脑膜炎引起的颞极白质双侧T2 FLAIR高信号的报告。在癌性脑膜炎患者中,异常的T2 FLAIR高信号可能并非源于缺血或肿瘤对实质的侵犯。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4aab/11512452/62399a28980a/fneur-15-1471668-g0001.jpg

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