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干燥综合征:五例系列报道

Sjogren's Syndrome: A Series of Five Cases.

作者信息

Naphade Pravin, Rohatgi Shalesh, Rao Prajwal, Nirhale Satish

机构信息

Neurology, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Pune, IND.

出版信息

Cureus. 2024 Oct 15;16(10):e71572. doi: 10.7759/cureus.71572. eCollection 2024 Oct.

Abstract

Sjogren's syndrome is an autoimmune disorder that has a prominent involvement of exocrine glands. Systemic involvement of other organs can also happen. Peripheral nervous system involvement is common and may present as axonal sensory/sensorimotor or demyelinating polyneuropathy, mononeuritis multiplex, ganglionopathy, or cranial neuritis. It can also present with transverse myelitis, especially longitudinally extensive transverse myelitis in association with aquaporin-4 antibodies. It can also mimic central nervous system (CNS) demyelinating disorders such as multiple sclerosis. The present case series highlights some uncommon neurological presentations of Sjogren's syndrome. In this series, patients presented with Miller-Fischer syndrome, recurrent Guillain-Barre syndrome, multifocal dystonia, and demyelinating disorder of CNS. None of the cases had presenting complaints of dry mouth or eyes. Special investigations such as magnetic resonance imaging (MRI), nerve conduction studies, anti-ganglioside panel, and cerebrospinal fluid analysis, depending on the clinical presentation of the cases, were conducted. Schirmer's test, tear breakup time, antinuclear antibodies (ANA) by immunofluorescent assay, ANA blot demonstrating the presence of anti-SSA (Ro) and/or anti-SSB (La) antibodies, and lip biopsy were conducted in all cases, which confirmed the diagnosis of Sjogren's syndrome. After the diagnosis was confirmed, other tests such as C- reactive protein, serum cryoglobulin, and rheumatoid factor were conducted. Treatment was initiated with steroids, followed by long-term immunosuppression with injection rituximab. Sjogren's syndrome may present with various presentations of neurological involvement, sometimes rare, and hence a high degree of suspicion is required when other usual causes are excluded.

摘要

干燥综合征是一种自身免疫性疾病,主要累及外分泌腺。其他器官也可能出现全身性受累。周围神经系统受累很常见,可表现为轴索性感觉/感觉运动性或脱髓鞘性多发性神经病、多发性单神经炎、神经节病或颅神经炎。它也可表现为横贯性脊髓炎,尤其是与水通道蛋白4抗体相关的纵向广泛横贯性脊髓炎。它还可能类似中枢神经系统(CNS)脱髓鞘疾病,如多发性硬化症。本病例系列突出了干燥综合征一些不常见的神经学表现。在这个系列中,患者表现为米勒-费希尔综合征、复发性吉兰-巴雷综合征、多灶性肌张力障碍和中枢神经系统脱髓鞘疾病。所有病例均无口干或眼干的主诉。根据病例的临床表现,进行了特殊检查,如磁共振成像(MRI)、神经传导研究、抗神经节苷脂检测和脑脊液分析。所有病例均进行了施密特试验、泪膜破裂时间、免疫荧光法检测抗核抗体(ANA)、显示抗SSA(Ro)和/或抗SSB(La)抗体存在的ANA印迹以及唇腺活检,这些检查确诊了干燥综合征。确诊后,进行了其他检查,如C反应蛋白、血清冷球蛋白和类风湿因子检测。治疗首先使用类固醇,随后长期使用注射用利妥昔单抗进行免疫抑制。干燥综合征可能表现为各种神经受累表现,有时很罕见,因此在排除其他常见病因时需要高度怀疑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/181c/11564634/623d09fcb320/cureus-0016-00000071572-i01.jpg

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