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Acute necrotizing retinal vasculitis as onset of systemic lupus erythematosus: A case report

机译:急性坏死性视网膜血管炎作为系统性红斑狼疮的发作:一例报告

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Rationale: Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by autoantibody production, complement activation, and deposition of immune complexes in tissues and organs. SLE can involve any region of the visual system. Although ocular manifestations are not part of the classification criteria for SLE, they can be observed in up to one-third of the patients with SLE. They are rarely reported at the time of disease onset. Retinal vasculitis is usually associated with active generalized disease. Due to its low frequency, we report a case of acute necrotizing retinal vasculitis as onset of SLE. Patient concerns and diagnosis: A 25-year-old white female was referred to the rheumatology clinic with gradually and rapid deterioration of the vision due to abnormal vessel permeability in the right fundus with edema along the vessels, occlusion of arterial branches in the middle periphery with leakage of the dye in these areas and indentical but less prominent changes with cotton wool spots in the papillomacular area and extensive hemorrhages in the left eye. The onset of malar rash, arthralgias and positive antinuclear, anti-double stranded DNA, anti-ribosomal P and anti-β2 glycoprotein I antibodies with decreased C4 complement levels, as well as the positive lupus-band test confirmed the diagnosis of SLE. Interventions: Aggressive immunomodulating therapy with high-dose methylprednisolone, intravenous immunoglobulin, and cyclophosphamide was used for suppression of the disease activity followed by azathioprine as maintaince therapy. Outcomes: Substantial improvement and partial resorption of the vasculitic changes, including central retinal artery and vein, was achieved prominently in the left eye. The study was conducted in accordance with the Declaration of Helsinki and written informed consent was obtained from the patient. Because of this, there is no need to conduct special ethic review and the ethical approval is not necessary. Lessons: Inclusion of ocular manifestations among the classification criteria for SLE would enable earlier establishment of the diagnosis and therapeutic interventions in some instances of SLE.
机译:原理:系统性红斑狼疮(SLE)是一种复杂的自身免疫性疾病,其特征在于自身抗体的产生,补体激活以及免疫复合物在组织和器官中的沉积。 SLE可以涉及视觉系统的任何区域。尽管眼部表现不是SLE分类标准的一部分,但在多达三分之一的SLE患者中可以观察到眼部表现。在疾病发作时很少报道它们。视网膜血管炎通常与活动性全身疾病相关。由于它的频率低,我们报道一例急性坏死性视网膜血管炎为SLE发作。患者关注和诊断:一名25岁的白人女性因风湿病在右眼底血管通透性异常,伴有沿血管的水肿,中枢动脉分支闭塞,导致视力逐渐迅速下降,转诊至风湿病门诊染料在这些区域的泄漏以及与之相同但不太明显的变化,如乳头状瘤区域的棉绒斑点和左眼的大量出血。黄斑疹,关节痛和抗核,抗双链DNA阳性,C4补体水平降低的抗核糖体P和抗β2糖蛋白I抗体的阳性以及狼疮带阳性试验的确证了SLE的诊断。干预措施:采用大剂量甲基强的松龙,静脉注射免疫球蛋白和环磷酰胺的积极免疫调节疗法可抑制疾病活动,随后使用硫唑嘌呤作为维持疗法。结果:左眼明显改善了包括中央视网膜动脉和静脉在内的血管变化的实质性改善和部分吸收。该研究是根据赫尔辛基宣言进行的,并获得了患者的书面知情同意。因此,无需进行特殊的道德审查,也无需道德批准。经验教训:将眼部表现包括在SLE的分类标准中,可以在SLE的某些情况下更早地建立诊断和治疗干预措施。

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