Boban Jasmina, Ardalı Selin, Thurnher Majda M
Faculty of Medicine, Department for Radiology, University of Novi Sad, Hajduk Veljkova 3, Novi Sad, 21000, Serbia.
Department of Radiology, Hacettepe University Faculty of Medicine, Sıhhiye, 06100, Ankara, Turkey.
Neuroradiology. 2018 Jul;60(7):769-773. doi: 10.1007/s00234-018-2028-y. Epub 2018 May 7.
Immunoglobulin G4 (IgG4)-related disease represents a spectrum of fibro-inflammatory disorders that affects various organ systems, including the central nervous system.
Here we present the case of lgG4-related hypertrophic meningitis with exclusively leptomeningeal involvement and spread via perivascular spaces.
A 58-year-old male patient presented with complex partial seizures. Initial computed tomography examination showed left frontal sulcal hyperdensity. Subsequent magnetic resonance examination revealed FLAIR hyperintensity in the central sulcus, with post-contrast enhancement in the form of "dotted line." Physical examination, routine laboratory, and cerebrospinal fluid analyses were unremarkable. Meningeal biopsy confirmed IgG4-related meningitis. After corticosteroid treatment, a complete resolution of imaging findings was observed. Two months later, the patient presented with relapsing neurological symptoms and radiological findings in postcentral, precentral, and temporal sulci, resembling the form of "dotted line" contrast enhancement. In addition, linear intraparenchymal enhancement that followed perivascular spaces was seen in the left parietal lobe. After repeated steroid therapy, all lesions resolved completely.
We reported the first case of isolated IgG4-related leptomeningeal involvement with a "dotted line" enhancement and perivascular intraparenchymal spread. Although IgG4-related meningitis represents a rare disease, both clinicians and radiologists should include this condition in the differential diagnosis of unclear leptomeningeal disease.
免疫球蛋白G4(IgG4)相关疾病是一种影响包括中枢神经系统在内的多个器官系统的纤维炎症性疾病谱。
本文报告一例IgG4相关肥厚性脑膜炎,仅累及软脑膜并通过血管周围间隙扩散。
一名58岁男性患者出现复杂部分性发作。最初的计算机断层扫描检查显示左侧额叶脑沟高密度影。随后的磁共振检查显示中央沟在液体衰减反转恢复序列(FLAIR)上呈高信号,增强扫描呈“虚线”样强化。体格检查、常规实验室检查和脑脊液分析均无异常。脑膜活检证实为IgG4相关脑膜炎。皮质类固醇治疗后,影像学表现完全消失。两个月后,患者出现复发的神经症状,中央后回、中央前回和颞叶脑沟出现类似“虚线”样强化的影像学表现。此外,左侧顶叶可见沿血管周围间隙的脑实质内线性强化。再次给予类固醇治疗后,所有病变完全消失。
我们报告了首例孤立的IgG4相关软脑膜受累伴“虚线”样强化及血管周围脑实质内扩散的病例。尽管IgG4相关脑膜炎是一种罕见疾病,但临床医生和放射科医生在鉴别诊断不明原因的软脑膜疾病时均应考虑此病。