由抗磷脂综合征引发的急性 Q 热:病例报告

La Revue de medecine interne Pub Date : 2024-07-01 Epub Date: 2024-05-17 DOI:10.1016/j.revmed.2024.05.006
K Balasoupramanien, J-B Roseau, N Cazes, C Surcouf, E Le Dault
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摘要

简介Q 热是一种由烧伤柯西氏菌引起的人畜共患疾病。急性感染主要无症状。在其他情况下,它主要引起流感样疾病、肺炎或肝炎。我们报告了一例以大量胸腔积液为表现的急性 Q 热的非典型病例:我们报告了一例因急性呼吸窘迫转诊至我院的 43 岁男性病例。进一步分析表明,患者有渗出性嗜酸性粒细胞胸腔积液,并伴有肺栓塞和股深静脉血栓形成。病原学调查显示,急性 Q 热(针对烧伤弧菌第二阶段抗原的 IgM 和 IgG)与抗磷脂有关。使用维生素 K 拮抗剂、强力霉素和羟氯喹后,直到抗磷脂抗体呈阴性,治疗效果良好:讨论与结论:在烧伤梭菌急性感染期间,抗磷脂抗体非常普遍,但血栓并发症却很少见。2023 年 ACR/EULAR APS 标准限制了 APS 的诊断,就像我们的急性重症感染病例一样。在非典型肺炎和/或血栓事件面前,对烧伤桿菌和抗磷脂抗体进行筛查可能是有用的。鉴于其证据水平较低,有学者讨论了用强力霉素、羟氯喹和抗凝剂延长治疗烧伤弧菌相关抗磷脂综合征的方法,但在我们的病例中取得了成功。
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Acute Q fever revealed by an anti-phospholipid syndrome: A case report.

Introduction: Q fever is a zoonosis caused by Coxiella burnetii. Acute infection is mainly asymptomatic. In other cases it mainly causes a flu-like illness, a pneumonia, or an hepatitis. We present an atypical case of an acute Q fever revealed by a massive pleural effusion.

Case report: We report the case of a 43-year-old man referred to our hospital for an acute respiratory distress. Further analyses showed an exudative eosinophilic pleural effusion, associated with a pulmonary embolism and a deep femoral vein thrombosis. Aetiologic explorations revealed an acute Q fever (IgM and IgG against C. burnetii phase II antigens) associated with anti-phospholipids. The outcome was favorable with vitamin K antagonists, doxycycline, and hydroxychloroquine, till the negativation of the anti-phospholipid antibodies.

Discussion and conclusion: During acute C. burnetii infections, anti-phospholipid antibodies are highly prevalent but thrombotic complications are rare. The 2023 ACR/EULAR APS criteria restricts the diagnosis of APS, as in our case of acute severe infection. In front of an atypical pneumonia and/or thrombotic events, screening of C. burnetii and anti-phospholipid antibodies could be useful. Given its low level of evidence, prolongated treatment by doxycycline, hydroxychloroquine ± anticoagulant for C. burnetii's associated anti-phospholipid syndrome is discussed, but succeeded in our case.

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