Okano Atsushi, Kanai Masahiro, Kita Takanobu, Nakai Yoshiyuki, Okada Hiroaki, Yamaguchi Keiji
Department of Neurology, Ichinomiya-Nishi Hospital.
Rinsho Shinkeigaku. 2021 Dec 22;61(12):856-861. doi: 10.5692/clinicalneurol.cn-001655. Epub 2021 Nov 18.
An 82-year-old man presented with subacute bilateral lower limb paralysis, deep sensory disturbance, and vesico-rectal disturbance. MRI of the spinal cord revealed a large gray matter-dominant lesion extending from the medulla oblongata to the lower thoracic spinal cord. The patient was treated with steroid-pulse therapy for myelitis, but without symptomatic improvement. A spinal cord biopsy was performed for treatment-resistant myelopathy, and histopathology revealed a diffuse large B-cell lymphoma, that was diagnosed as a primary intramedullary spinal cord lymphoma because systemic examination didn't show any other findings suggestive of malignant lymphoma. A spinal cord biopsy is necessary for the definitive diagnosis of this disease, but in the case of poor response to treatment and a progressive course, intramedullary malignant lymphoma should be considered if there is a persistent elevation of CSF IL-10 or a prolonged contrast effect.
一名82岁男性出现亚急性双侧下肢瘫痪、深感觉障碍及膀胱直肠功能障碍。脊髓MRI显示一个以灰质为主的大病灶,从延髓延伸至下胸段脊髓。患者接受了脊髓炎的类固醇冲击治疗,但症状无改善。因难治性脊髓病进行了脊髓活检,组织病理学显示为弥漫性大B细胞淋巴瘤,由于全身检查未发现任何其他提示恶性淋巴瘤的迹象,故诊断为原发性髓内脊髓淋巴瘤。脊髓活检对于该病的确诊是必要的,但在治疗反应不佳且病情进展的情况下,如果脑脊液IL-10持续升高或造影剂效应持续时间延长,则应考虑髓内恶性淋巴瘤。