Bilateral Periorbital Erythema and Swelling as an Initial Presentation of Systemic Lupus Erythematosus: A Rare Case.

IF 1.2 Q4 RHEUMATOLOGY
Jitendra Singh, Anju Dinkar, Nilesh Kumar, Kailash Kumar, Isha Atam
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引用次数: 0

Abstract

Introduction: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by multisystem involvement due to autoantibody production and immune complex deposition. While classical cutaneous manifestations, such as malar rash, are common, atypical presentations, like periorbital erythema and swelling, are rare and pose diagnostic challenges. Early recognition is crucial to prevent disease progression and complications.

Case presentation: A 16-year-old girl presented with a three-month history of intermittent bilateral periorbital swelling. Clinical examination revealed pallor and localized alopecia with no significant systemic abnormalities. Laboratory investigations showed pancytopenia with normal renal, hepatic, and thyroid functions and unremarkable urinalysis, chest X-ray, and ECG. Autoimmune markers were positive, with a strongly positive ANA titer of 1:1000 and significantly elevated anti- dsDNA antibodies of 380 IU/mL (reference range: 0-200 IU/mL). According to the 2019 EULAR/ ACR classification criteria, a diagnosis of SLE was established. The patient was treated with pulse intravenous methylprednisolone (1g daily for three days), followed by oral prednisolone (1 mg/kg/day), in a tapering regimen and hydroxychloroquine at standard doses. She showed marked improvement, with resolution of periorbital swelling, recovery of pancytopenia, and hair regrowth. At two-month follow-up, she remained asymptomatic and continued hydroxychloroquine for maintenance therapy.

Conclusion: This case underscores the importance of considering SLE in patients with atypical presentations, like periorbital erythema and pancytopenia. Early diagnosis based on clinical and serological findings, followed by appropriate therapy, can achieve remission and prevent complications. The case highlights the need for heightened clinical suspicion and multidisciplinary management in young patients.

双侧眼眶周围红斑和肿胀作为系统性红斑狼疮的初始表现:一个罕见的病例。
系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病,其特点是自身抗体产生和免疫复合物沉积累及多系统。虽然典型的皮肤表现,如颧红疹是常见的,但非典型的表现,如眼眶周围红斑和肿胀,是罕见的,并构成诊断挑战。早期识别对于预防疾病进展和并发症至关重要。病例介绍:一个16岁的女孩提出了三个月的间歇性双侧眼眶周围肿胀的历史。临床检查显示苍白和局部脱发,无明显的全身异常。实验室检查显示全血细胞减少,肾、肝、甲状腺功能正常,尿液分析、胸部x线和心电图无明显异常。自身免疫标志物呈阳性,ANA滴度为1:1000强阳性,抗dsDNA抗体显著升高380 IU/mL(参考范围:0-200 IU/mL)。根据2019年EULAR/ ACR分类标准,建立SLE诊断。患者接受脉搏静脉注射甲基强的松龙(每日1g,连用3天),随后口服强的松龙(1mg /kg/天),逐渐减少治疗方案,并以标准剂量羟氯喹治疗。她表现出明显的改善,眼眶周围肿胀消退,全血细胞减少症恢复,头发再生。随访2个月,患者无症状,继续使用羟氯喹维持治疗。结论:该病例强调了考虑SLE患者非典型表现的重要性,如眼眶周围红斑和全血细胞减少症。基于临床和血清学发现的早期诊断,然后进行适当的治疗,可以达到缓解和预防并发症。该病例强调了对年轻患者加强临床怀疑和多学科管理的必要性。
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来源期刊
CiteScore
2.30
自引率
0.00%
发文量
82
期刊介绍: Current Rheumatology Reviews publishes frontier reviews on all the latest advances on rheumatology and its related areas e.g. pharmacology, pathogenesis, epidemiology, clinical care, and therapy. The journal"s aim is to publish the highest quality review articles dedicated to clinical research in the field. The journal is essential reading for all researchers and clinicians in rheumatology.
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