Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.
Neuropathology. 2022 Aug;42(4):295-301. doi: 10.1111/neup.12807. Epub 2022 May 23.
Neurolymphomatosis is a neurological manifestation of lymphoma that involves the cranial or spinal peripheral nerves, nerve roots, and plexus with direct invasion of neoplastic cells. Neurolymphomatosis is rare among patients with low-grade lymphoma. We report an autopsied case of neurolymphomatosis that arose from follicular lymphoma. A 49-year-old woman who presented with pain of her neck and shoulder and numbness of her chin. Computed tomography revealed enlarged lymph nodes in her whole body, and biopsy from the axillary lymph node revealed grade 2 follicular lymphoma. Although the patient underwent chemotherapy, she gradually developed muscle weakness in the upper limbs and sensory disturbances of the trunk and limbs. F-fluorodeoxyglucose positron emission tomography (FDG-PET) revealed increased tracer uptake of the cervical nerve roots. Repeated FDG-PET after additional therapy revealed progression of disease within the nerve roots and brachial plexus, whereas gadolinium-contrast magnetic resonance imaging (MRI) showed weak enhancement of the cervical nerve roots without formation of mass lesions. She died after a total disease duration of 12 months. Postmortem observations revealed invasion of lymphoma cells into the cervical nerve roots, dorsal root ganglia, and subarachnoid spaces of the spinal cord. Neurolymphomatosis was prominent at the segments of C6-Th2. Combined loss of axons and myelin sheaths was observed in the cervical nerve roots and posterior columns. Lymphoma cells also invaded the cranial nerves. The subarachnoid and perivascular spaces of the brain demonstrated focal invasion of the lymphoma. Mass lesions were not observed in the central nervous system. The lymphoma cells did not show histological transformation to higher grades, and the density of the centroblasts remained at grade 2. Our report clarifies that low-grade follicular lymphoma can manifest as neurolymphomatosis and central nervous system invasion in the absence of transformation toward higher histological grades. FDG-PET may be more sensitive to non-mass-forming lesions, including neurolymphomatosis, than gadolinium-contrast MRI.
神经淋巴病是淋巴瘤的一种神经系统表现,涉及颅神经或脊神经周围神经、神经根和神经丛,伴有肿瘤细胞的直接侵犯。神经淋巴病在低级别淋巴瘤患者中较为罕见。我们报告一例由滤泡性淋巴瘤引起的神经淋巴病尸检病例。一名 49 岁女性,表现为颈部和肩部疼痛以及下巴麻木。计算机断层扫描显示全身淋巴结肿大,腋窝淋巴结活检显示 2 级滤泡性淋巴瘤。尽管患者接受了化疗,但她逐渐出现上肢肌无力和躯干及四肢感觉障碍。氟-脱氧葡萄糖正电子发射断层扫描(FDG-PET)显示颈椎神经根摄取示踪剂增加。在追加治疗后再次进行 FDG-PET 检查显示神经根和臂丛内疾病进展,而钆增强磁共振成像(MRI)显示颈椎神经根增强较弱,无肿块形成。患者在总病程 12 个月后死亡。尸检观察到淋巴瘤细胞侵犯颈椎神经根、背根神经节和脊髓蛛网膜下腔。神经淋巴病在 C6-Th2 节段较为突出。颈椎神经根和后柱可见轴突和髓鞘联合丧失。淋巴瘤细胞还侵犯颅神经。大脑蛛网膜下腔和血管周围间隙显示淋巴瘤的局灶性侵犯。中枢神经系统未见肿块形成。淋巴瘤细胞未发生组织学转化为更高等级,中心母细胞密度仍为 2 级。我们的报告阐明了低级别滤泡性淋巴瘤可表现为神经淋巴病和中枢神经系统侵犯,而无向更高组织学等级转化。FDG-PET 对非肿块形成病变(包括神经淋巴病)的敏感性可能高于钆增强 MRI。