Schnitzler Syndrome after COVID-19 Vaccination

Mizuki Asako, H. Matsunaga, K. Oka, S. Ueda
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引用次数: 2

Abstract

An 86-year-old Japanese woman was referred for an examination of leukocytosis and diagnosed with Waldenström macroglobulinemia. She was asymptomatic and remained stable during follow-up without treatment. The day after receiving her first COVID-19 vaccination (Pfizer-BioNTech), she developed urticarial exanthema on her limbs. Although the rash improved with topical steroids, it worsened the day after she received the second vaccination; bone pain, general fatigue, and leukocytosis (white blood cell count: 11,600/ μL) also developed. A skin biopsy showed perivascular and interstitial neutrophil infiltrate with leukocytoclasia (Picture A, B), and definite Schnitzler syndrome was diagnosed according to the Strasbourg criteria (1). She rapidly responded to low-dose prednisolone (10 mg/day), and the skin rash and systemic symptoms resolved. Schnitzler syndrome is autoinflammatory and characterized by urticarial rash and immunoglobulin M monoclonal gammopathy. Lymphoproliferative disorders feature immune dysregulation that often results in autoimmune disease (2). In patients with lymphoproliferative disorders, physicians should pay careful attention to immune complications after COVID-19 vaccination.
COVID-19疫苗接种后的施尼茨勒综合征
一位86岁的日本妇女因白细胞增多症被诊断为Waldenström巨球蛋白血症。患者无症状,随访期间病情稳定。在她第一次接种COVID-19疫苗(辉瑞- biontech)的第二天,她的四肢出现了荨麻疹。虽然局部类固醇改善了皮疹,但在她接受第二次疫苗接种的第二天,皮疹恶化了;骨痛、全身乏力、白细胞增多(白细胞计数:11600 / μL)。皮肤活检显示血管周围和间质中性粒细胞浸润伴白细胞减少(图A、B),根据斯特拉斯堡标准诊断为明确的施尼茨勒综合征(1)。低剂量强的松龙(10mg /天)治疗后迅速反应,皮疹和全身症状消失。施尼茨勒综合征是一种自身炎症,以荨麻疹和免疫球蛋白M单克隆γ病为特征。淋巴细胞增生性疾病以免疫失调为特征,常导致自身免疫性疾病(2)。对于淋巴细胞增生性疾病患者,医生应注意COVID-19疫苗接种后的免疫并发症。
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