Department of Neurology, Tokyo Metropolitan Neurological Hospital, Japan.
Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Japan.
Intern Med. 2021 Jun 15;60(12):1941-1947. doi: 10.2169/internalmedicine.6461-20. Epub 2021 Jan 15.
Due to its rarity and the limited literature, the clinicopathological characteristics of peripheral nerve involvement in immunoglobulin G4 (IgG4)-related disease are unknown. We present two cases of IgG4-related disease, accompanied by peripheral neuropathy, presenting as unilateral ptosis (case 1) and sclerosing cholangitis (case 2), respectively. In both cases, sural nerve biopsy indicated vasculitis as the underlying pathophysiology; the peripheral neuropathy was refractory to corticosteroid therapy. In contrast to the previously proposed pathomechanism of IgG4-related neuropathy (direct lymphoplasmacytic infiltration), the pathological findings in our cases suggest that vasculitis occurs secondary to systemic autoimmune conditions.
由于其罕见性和文献有限,免疫球蛋白 G4(IgG4)相关疾病中周围神经受累的临床病理特征尚不清楚。我们报告了两例 IgG4 相关疾病伴周围神经病的病例,分别表现为单侧上睑下垂(病例 1)和硬化性胆管炎(病例 2)。在这两种情况下,腓肠神经活检均表明血管炎是潜在的病理生理学基础;周围神经病对皮质类固醇治疗无反应。与之前提出的 IgG4 相关神经病的发病机制(直接淋巴浆细胞浸润)不同,我们的病例中的病理发现表明血管炎继发于系统性自身免疫性疾病。