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一名患有系统性红斑狼疮且抗磷脂抗体阴性的女性患者出现脾梗死——一例罕见病例报告。

Splenic infarcts in a lady with systemic lupus erythematosus and negative antiphospholipid antibodies-A rare case report.

作者信息

Ashour Amr, Faisal Mohanad, Ibrahim Elmunzer, Al-Madani Mohammed

机构信息

Department of Medical Education Hamad Medical Corporation Doha Qatar.

Department of Internal Medicine Hamad Medical Corporation Doha Qatar.

出版信息

Clin Case Rep. 2023 Mar 19;11(3):e7092. doi: 10.1002/ccr3.7092. eCollection 2023 Mar.

Abstract

Systemic lupus erythematosus is a multisystem autoimmune disease associated with a variety of arterial and venous thrombotic manifestations when combined with antiphospholipid syndrome. We present a case report of a 23-year-old female patient with a recent diagnosis of systemic lupus erythematosus who was admitted for abdominal pain and later diagnosed with splenic infarction via abdominal computed tomography. This was the only hematologic manifestation, with no prior history of thrombotic events or antiphospholipid antibodies.

摘要

系统性红斑狼疮是一种多系统自身免疫性疾病,与抗磷脂综合征合并时会出现多种动脉和静脉血栓形成表现。我们报告一例23岁女性患者,近期诊断为系统性红斑狼疮,因腹痛入院,随后经腹部计算机断层扫描诊断为脾梗死。这是唯一的血液学表现,既往无血栓形成事件或抗磷脂抗体病史。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3fe/10025247/a79a33b96f01/CCR3-11-e7092-g001.jpg

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