When a Rapid Accurate Diagnosis Changes Therapeutic Approach: Recognizing Acute Abdominal Pain with Ascites as a Possible Presentation of Systemic Lupus Erythematosus.

Szu-Cheng Huang, Yi-Ling Chan, Hao-Tsai Cheng, Zhong Ning Leonard Goh, Yon-Cheong Wong, Chen-Ken Seak, Joanna Chen-Yeen Seak, Chih-Huang Li, Hsien-Yi Chen, Chen-June Seak
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Abstract

Systemic lupus erythematosus (SLE) is a chronic, multi-organ autoimmune disease which rarely presents with peritoneal involvement. As such, its diagnosis in the emergency department (ED) based on a clinical presentation of gastrointestinal symptoms is extremely challenging. Yet, reaching such a diagnosis in the ED is crucial for avoiding unnecessary surgical intervention and initiating early glucocorticoid therapy to maximise patient outcomes. Here, we report a case of newly diagnosed SLE in a 28-year-old lady who presented atypically and unusually with abdominal pain and ascites. She required extensive but methodical investigations, and was eventually diagnosed with lupus mesenteric vasculitis with underlying newly diagnosed SLE in the ED. The patient was promptly treated with methylprednisolone resulting in marked clinical improvement. Emergency physicians should be mindful of abdominal pain with ascites as an extremely rare but important clinical presentation of SLE. Early diagnosis and commencement of glucocorticoid therapy in these patients are crucial in halting disease progression and averting the need for surgical intervention.

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当快速准确的诊断改变了治疗方法:认识到急性腹痛并腹水可能是系统性红斑狼疮的表现。
系统性红斑狼疮(SLE)是一种慢性、多器官自身免疫性疾病,很少表现为累及腹膜。因此,根据胃肠道症状的临床表现在急诊科(ED)诊断是极具挑战性的。然而,在急诊科中达到这样的诊断对于避免不必要的手术干预和早期开始糖皮质激素治疗以最大化患者预后至关重要。在这里,我们报告一个28岁的女性新诊断的SLE病例,她表现出不典型和不寻常的腹痛和腹水。她需要进行广泛而系统的调查,最终被诊断为狼疮肠系膜血管炎,并伴有ED中新诊断的SLE。患者立即接受甲基强的松龙治疗,临床明显改善。急诊医师应注意腹痛并腹水是SLE极为罕见但重要的临床表现。这些患者的早期诊断和开始糖皮质激素治疗对于阻止疾病进展和避免手术干预的需要至关重要。
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