Sihvonen Aleksi J, Laakso Sini M, Tynninen Olli, Saaren-Seppälä Heikki, Löfberg Mervi
Department of Neurology, Neurocenter, Helsinki University Central Hospital, Haartmaninkatu 4, P.O. Box 340, 00029 Helsinki, Finland.
Clinical Neurosciences, Neurology, University of Helsinki and Brain Center, Helsinki University Hospital, Helsinki, Finland.
Ther Adv Neurol Disord. 2023 Jul 18;16:17562864231186091. doi: 10.1177/17562864231186091. eCollection 2023.
IgG4-related disease (IgG4-RD) is an emerging immune-mediated chronic fibrotic disease characterized by tumour-like mass formation. Reports of brain parenchymal involvement in IgG4-RD are rare and complete treatment-related remission of lesions has never been reported. Here, we present a woman in her mid-50s who developed headache and seizures. Brain magnetic resonance imaging revealed frontal bilateral pachymeningitis and a left frontal lobe parenchymal lesion, and pathologic findings were consistent with an IgG4-RD central nervous system manifestation. She had a history of tumour-like growth around the right optic nerve, orbital and maxillary cavities treated successfully with corticosteroids 28 years ago, and was receiving infliximab as a maintenance therapy for uveitis for the last 14 years. After initial high-dose corticosteroid treatment, the patient was treated with rituximab, and after 3 months, the patient presented with complete remission of IgG4-RD lesions and associated symptoms. This case illustrates the chronic, decades-spanning nature of IgG4-RD, and a complete response to rituximab even with intracerebral mass lesions that had emerged despite the use of infliximab, a therapy previously reported successful in IgG4-RD.
IgG4相关性疾病(IgG4-RD)是一种新出现的免疫介导的慢性纤维化疾病,其特征为肿瘤样肿块形成。脑实质受累于IgG4-RD的报道罕见,且从未有过与治疗相关的病变完全缓解的报道。在此,我们报告一名50多岁的女性,她出现头痛和癫痫发作。脑部磁共振成像显示双侧额叶硬脑膜炎和左侧额叶实质病变,病理结果与IgG4-RD的中枢神经系统表现一致。她有28年前曾成功接受皮质类固醇治疗的右侧视神经、眼眶和上颌窦周围肿瘤样生长病史,并且在过去14年中一直在接受英夫利昔单抗作为葡萄膜炎的维持治疗。在最初的高剂量皮质类固醇治疗后,患者接受了利妥昔单抗治疗,3个月后,患者出现IgG4-RD病变及相关症状完全缓解。该病例说明了IgG4-RD的慢性、长达数十年的病程特点,以及即使存在尽管使用了此前报道在IgG4-RD中成功的英夫利昔单抗仍出现的脑内肿块病变,利妥昔单抗仍能产生完全反应。