系统性红斑狼疮合并急性胰腺炎的异常表现:1例报告

Majed Saleh Alanazi, Ahmed Hameed Alreshidi, Hamoud Fahad Aldhamadi, Yasir Saleh Alrashidi, Abdulaziz Khalid Alshammari
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引用次数: 0

摘要

系统性红斑狼疮(SLE)是一种影响任何器官的慢性自身免疫性疾病,具有多种临床表现。狼疮相关性急性胰腺炎(AP)是sle引起的急性腹部不适的严重原因,同时伴有狼疮肠系膜血管炎。系统性红斑狼疮(SLE)是一种复杂的慢性自身免疫性疾病,其特点是其能够影响几乎任何器官系统,导致广泛的临床表现。狼疮相关性急性胰腺炎(AP)是SLE的一个特别严重的并发症,可引起急性腹部不适。狼疮肠系膜血管炎是SLE的另一腹部表现,进一步突出了该疾病的全身性。狼疮性胰腺炎在女性和30岁以上人群中更为常见,发病率从0.7%到4%不等。本病例报告描述了一名16岁的沙特女性,她因间歇性发烧、上腹部疼痛、出汗、食欲不振和腹泻等症状来到急诊科。她的实验室检查结果显示白细胞减少,贫血,肝脏和胰腺酶水平升高,炎症标志物升高,补体不足。在排除了其他潜在原因后,她被诊断出患有狼疮性胰腺炎。治疗包括类固醇和羟氯喹。患者所有症状均有明显改善,强调及时诊断和处理的必要性。本病例坚持及时诊断和适当治疗,以减轻狼疮性胰腺炎和其他sle相关并发症的潜在严重后果。总之,SLE是一种多方面的自身免疫性疾病,影响包括胰腺在内的各个器官,导致狼疮性胰腺炎等疾病。本病例深刻地提醒了SLE临床表现的多样性,并强调了及时诊断和有效管理在改善患者预后方面的关键作用。
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Unusual Presentation of Systemic Lupus Erythematosus with Acute Pancreatitis: A Case Report
Systemic Lupus Erythematosus (SLE) is a chronic autoimmune disease affecting any organ with diverse clinicalmanifestations. Lupus-related acute pancreatitis (AP) is a serious cause of SLE-induced acute abdominal discomfort, along with lupusmesenteric vasculitis. Systemic Lupus Erythematosus (SLE) is a complex and chronic autoimmune disease characterized by its ability toaffect virtually any organ system, resulting in a wide array of clinical manifestations. One particularly severe complication associatedwith SLE is lupus-related acute pancreatitis (AP), which can cause acute abdominal discomfort. Lupus mesenteric vasculitis is anotherabdominal manifestation of SLE, further highlighting the systemic nature of the disease. Lupus pancreatitis is more common in femalesand the third decade of life, with an incidence ranging from 0.7% to 4%. This case report describes a 16-year-old Saudi female whopresented to the emergency department with episodic fever, epigastric abdominal pain, sweating, loss of appetite, and diarrhoea,among other symptoms. Her laboratory test results showed leukopenia, anaemia, increased liver, and pancreatic enzyme levels,increased inflammatory markers, and hypocomplementemia. She was diagnosed with lupus pancreatitis after ruling out other potentialcauses. Treatment included steroids and hydroxychloroquine. The patient showed marked improvement in resolving all symptoms,emphasizing the need for prompt diagnosis and management. This case insists on timely diagnosis and appropriate management inmitigating the potentially severe consequences of lupus pancreatitis and other SLE-related complications. In conclusion, SLE is amultifaceted autoimmune condition that affects various organs, including the pancreas, leading to conditions like lupus pancreatitis.The presented case serves as a poignant reminder of the diverse clinical presentations of SLE and highlights the crucial role of promptdiagnosis and effective management in improving patient outcomes.
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