Borges Alexandra, Garcez Daniela, Pedro Cátia, Passos João
Radiology Department, Instituto Português de Oncologia Francisco Gentil, Centro de Lisboa, Rua Prof. Lima Basto, 1099-023 Lisbon, Portugal.
Radiology Department, Champalimaud Foundation for the unknown, Av. Brasília, 1400-038 Lisbon, Portugal.
eNeurologicalSci. 2021 Jan 20;22:100315. doi: 10.1016/j.ensci.2021.100315. eCollection 2021 Mar.
We report the case of a 28-year-old man, diagnosed with a non-secreting, non-metastatic suprasellar germinoma treated with chemoradiation who developed, four months after completion of radiation therapy, multiple discrete demyelinating lesions mimicking multiple sclerosis (MS). The patient had no previous diagnosis of MS and the neuroimaging studies performed both at the time of diagnosis and after chemotherapy, pre-irradiation, showed no evidence of white matter lesions. He remained asymptomatic, with no focal neurological deficits. Biochemical analysis of the CSF was positive for the intrathecal synthesis of IgG with oligoclonal bands. Follow-up MRI six months later showed a spontaneous decrease in lesion size and resolution of associated inflammatory signs, with lesions remaining stable in number. We discuss the potential origin of these white matter lesions, which may correspond to MS-like late-delayed demyelination secondary to chemoradiation therapy, in a previously predisposed patient.
我们报告了一例28岁男性病例,该患者被诊断为非分泌性、非转移性鞍上生殖细胞瘤,接受了放化疗,在放疗结束四个月后出现了多个散在的脱髓鞘病变,酷似多发性硬化症(MS)。该患者既往无MS诊断,诊断时及化疗后、放疗前进行的神经影像学检查均未显示白质病变迹象。他没有症状,也没有局灶性神经功能缺损。脑脊液的生化分析显示鞘内IgG合成及寡克隆带呈阳性。六个月后的随访MRI显示病变大小自发减小,相关炎症体征消退,病变数量保持稳定。我们讨论了这些白质病变的潜在起源,在先前易患的患者中,可能与放化疗继发的类似MS的迟发性脱髓鞘有关。