Pawar Priti, Kanyal Deepika, Kadam Abhinav, Khare Shweta
Department of Hospital Administration, Datta Meghe Institute of Higher Education and Research, Wardha, IND.
Department of Medicine, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.
Cureus. 2024 Jul 31;16(7):e65905. doi: 10.7759/cureus.65905. eCollection 2024 Jul.
Neurological complications are observed less frequently with primary Sjögren syndrome (SS). The central nervous system (CNS) has seldom been shown to exhibit symptoms of SS, making the diagnosis of SS with neurological involvement difficult. We present a rare case scenario in which a young 23-year-old male presenting with an acute history of fever, headache, vomiting, altered sensorium, and seizures was admitted and diagnosed as a sub-acute infarct in the right frontal-parietal-temporal lobes on a computed tomography (CT) scan. Upon further examination, laboratory investigations were suggestive of viral encephalitis. The patient was treated accordingly with antiviral drugs, and the patient improved. The patient took "discharge against medical advice" after 12 days, only to return to the hospital with similar complaints within 15 days. Magnetic resonance imaging (MRI) was done, which suggested an acute evolving infarct in the right frontal and parietal lobe, and further evaluation yielded a diagnosis of SS. The patient was treated with high-dose steroids for seven days. A repeat MRI showed new acute infarcts with dilatation of the ventricular system with periventricular ooze. The patient could not be revived and succumbed after one week of steroid therapy.
原发性干燥综合征(SS)较少出现神经并发症。中枢神经系统(CNS)很少表现出SS症状,使得诊断伴有神经受累的SS很困难。我们报告一例罕见病例,一名23岁年轻男性,有发热、头痛、呕吐、意识改变和癫痫发作的急性病史,入院后经计算机断层扫描(CT)诊断为右侧额顶颞叶亚急性梗死。进一步检查后,实验室检查提示为病毒性脑炎。患者接受了相应的抗病毒药物治疗,病情有所改善。患者在12天后“自动出院”,但在15天内又因类似症状返回医院。进行了磁共振成像(MRI)检查,提示右侧额叶和顶叶急性进展性梗死,进一步评估后确诊为SS。患者接受了七天的大剂量类固醇治疗。复查MRI显示有新的急性梗死灶,脑室系统扩张伴脑室周围渗出。患者在类固醇治疗一周后未能苏醒并死亡。