UnMASking the diagnosis: Acute severe necrotizing pancreatitis in the setting of systemic lupus erythematosus complicated by macrophage activation syndrome

C. Askin, J. Edelson, G. Dooley, A. Stratton
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Abstract

Systemic lupus erythematosus (SLE) is a common rheumatologic condition with known GI involvement. Acute pancreatitis (AP) is a rare GI complication of SLE and is typically associated with increased disease activity. Macrophage activation syndrome (MAS) is an unusual, hyper-inflammatory response to a rheumatologic stimulus characterized by hyperferritinemia, pancytopenia, thermal dysregulation and multi-organ dysfunction. MAS, more commonly seen in children, has been reported to complicate both adult onset SLE and AP. We present a case of necrotizing AP secondary to an SLE flare complicated by MAS in an adult patient successfully treated with anakinra.
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揭示诊断:急性重症坏死性胰腺炎在系统性红斑狼疮并发巨噬细胞激活综合征的设置
系统性红斑狼疮(SLE)是一种常见的风湿病,已知累及胃肠道。急性胰腺炎(AP)是SLE的一种罕见的胃肠道并发症,通常与疾病活动性增加有关。巨噬细胞激活综合征(MAS)是一种罕见的、对风湿病刺激的高炎症反应,其特征是高铁蛋白血症、全血细胞减少症、热失调和多器官功能障碍。MAS更常见于儿童,有报道称它会使成人发病的SLE和AP复杂化。我们报告了一例继发于SLE发作并MAS的坏死性AP,该患者为阿那白成功治疗的成人患者。
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