以脾梗死为表现的抗磷脂综合征和系统性红斑狼疮:病例报告

Johan Azañero-Haro , Liliana Chambi , Alonso Soto
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引用次数: 0

摘要

脾梗塞是一种罕见的疾病,通常与全身性疾病有关。抗磷脂综合征(APS)是一种自身免疫性疾病,可表现为脾梗塞引起的腹痛。我们描述了一名因急性腹痛入院的系统性红斑狼疮患者。腹部 CT 扫描显示脾梗塞,抗磷脂抗体和抗β2-糖蛋白 I 抗体检测呈阳性。本文讨论了与 APS 相关的脾梗死的病理生理学和临床表现,强调了将这种疾病纳入全身性疾病患者不明原因腹痛的鉴别诊断中的重要性。
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Splenic infarction as presentation of antiphospholipid syndrome and systemic lupus erythematosus: A case report

Splenic infarction is a rare condition usually associated with systemic conditions. Antiphospholipid syndrome (APS) is an autoimmune condition that can present as abdominal pain due to splenic infarction. We describe a patient with systemic lupus erythematosus, admitted due to acute abdominal pain. Abdominal CT scan showed splenic infarction, and tests for antiphospholipid and anti-β2-glycoprotein I antibodies were positive. The pathophysiology and clinical presentation of splenic infarction associated with APS is discussed, emphasizing the importance of including this entity in the differential diagnosis of abdominal pain of uncertain cause in patients with systemic conditions.

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