北京大学学报(医学版) ›› 2023, Vol. 55 ›› Issue (6): 1118-1124. doi: 10.19723/j.issn.1671-167X.2023.06.025
Jie WU,Wen ZHANG,Shu LIANG,Yi-lu QIN,Wen-qiang FAN*()
摘要:
原发性干燥综合征(primary Sjögren’s syndrome, pSS)的中枢神经系统受累少见, 常表现为脑白质病变、视神经脊髓炎谱系疾病(neuromyelitis optica spectrum disorder, NMOSD)或横贯性脊髓炎。NMOSD是一类免疫介导的中枢神经系统炎性脱髓鞘病变, 发病特点为高复发、高致残。pSS合并NMOSD患者病情更严重、预后更差。本研究报道1例pSS合并NMOSD妊娠期危重症的病例, 患者为有pSS病史的30岁孕妇, 被诊断为NMOSD, 在妊娠期接受甲泼尼龙琥珀酸钠、丙种球蛋白和硫酸羟氯喹片联合治疗, 治疗后患者出现口干、吞咽困难、腰背以下部位麻木感基本消失。患者于院外未规律服药, 右下肢出现无力、不能活动, 左下肢活动尚可, 偶伴麻木感。后急诊入院, 紧急行剖宫产分娩一健康男婴后, 患者病情加重, 高热伴双下肢瘫痪无力, 无法自主大小便。患者再次接受甲泼尼龙琥珀酸钠、丙种球蛋白治疗, 但症状改善不佳。首次给予利妥昔单抗输注后患者出现尿路感染, 予控制感染后继续规律输注利妥昔单抗, 后期患者行走略跛, 能够控制排尿和排便, 可正常工作。该病例表明, pSS合并NMOSD的妊娠期患者可考虑给予甲泼尼龙琥珀酸钠、丙种球蛋白和硫酸羟氯喹片联合治疗。利妥昔单抗可以明显改善NMSOD患者产后瘫痪、二便失禁等症状, 但同时可能有感染的风险。
中图分类号:
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