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神经精神性狼疮:一位肺结核患者的艰难历程

Neuropsychiatric Lupus: A Challenging Journey of a Patient With Pulmonary Tuberculosis.

作者信息

Chapra Ammar Farook, Khir Fadi, Alamami Ans, Salem Khaled M, Yusof Alhady

机构信息

Internal Medicine, Hamad Medical Corporation, Doha, QAT.

Internal Medicine Residency Program, Medical Education, Hamad Medical Corporation, Doha, QAT.

出版信息

Cureus. 2021 Jun 29;13(6):e16018. doi: 10.7759/cureus.16018. eCollection 2021 Jun.

Abstract

Systemic lupus erythematosus (SLE) is a disease that affects multiple systems in the body. Due to its variable manifestations, it can at times pose challenges for physicians to hold SLE as the culprit behind an affected system. This is most true when encountering patients with neuropsychiatric manifestations of SLE. We present a case of a 38-year-old female with known SLE limited to skin involvement and on treatment for active pulmonary tuberculosis (TB), yet otherwise healthy, who presented with acute fever associated with generalized tonic-clonic seizures. She was investigated for meningoencephalitis with a cerebrospinal fluid (CSF) analysis not being fully conclusive and with imaging features suggestive of viral encephalitis. However, despite receiving optimal care for causes of bacterial, viral, and tuberculous meningitis the patient continued to deteriorate and started to develop predominant psychiatric symptoms in the form of confusion and combative behavior requiring pharmacological restraint. Hence a trial of immunosuppressives was given with a presumptive diagnosis of neuropsychiatric lupus with IV methylprednisolone followed by a course of IV cyclophosphamide. However, this treatment proceeded with caution due to the fear of disseminated tuberculosis for which she did not show any sign of in the subsequent weeks. The patient showed modest clinical and radiological improvement and hence the treatment was continued. The case highlights the uncertainty that may precede a diagnosis of neuropsychiatric lupus and the challenges in treating it in patients with active mycobacterial infection.

摘要

系统性红斑狼疮(SLE)是一种影响身体多个系统的疾病。由于其表现多样,有时医生很难将SLE认定为某个受累系统的病因。在遇到有SLE神经精神症状的患者时尤其如此。我们报告一例38岁女性病例,该患者已知患有仅累及皮肤的SLE,正在接受活动性肺结核(TB)治疗,除此之外身体健康,她出现了伴有全身强直阵挛性发作的急性发热。对其进行了脑膜炎调查,脑脊液(CSF)分析结果不完全明确,影像学特征提示为病毒性脑炎。然而,尽管针对细菌性、病毒性和结核性脑膜炎的病因给予了最佳治疗,患者病情仍持续恶化,并开始出现以意识模糊和攻击行为为主的精神症状,需要药物约束。因此,在初步诊断为神经精神性狼疮的情况下,给予了免疫抑制剂试验性治疗,先静脉注射甲泼尼龙,随后静脉注射环磷酰胺。然而,由于担心播散性结核,治疗过程谨慎,在随后几周患者未表现出任何播散性结核迹象。患者临床和影像学表现有适度改善,因此继续进行治疗。该病例凸显了神经精神性狼疮诊断前可能存在的不确定性,以及在患有活动性分枝杆菌感染的患者中治疗该病的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b845/8320408/e1a2291be7b6/cureus-0013-00000016018-i01.jpg

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