药物致过敏反应表现为系统性毛细血管渗漏样综合征伴多浆液炎1例。

IF 2.1 Q3 RHEUMATOLOGY
Ninh Xuan Nguyen, Ngoc Tien Pham, Huong Thi Thanh Le, Quoc Viet Tran, Hang Ngoc Thuy Tran, An Thien Do
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引用次数: 0

摘要

背景:系统性毛细血管渗漏综合征(SCLS)是一种罕见的疾病,其特征是血管通透性增加导致液体和蛋白质的第三间距。药物引起的超敏反应在临床和放射学上可以模拟scs。病例介绍:一名42岁越南男性在接受幽门螺杆菌根除治疗后出现腹胀、面部水肿和呼吸困难。影像显示胸膜、心包及腹膜积液、门静脉周围水肿及间质性肺水肿。实验室结果显示低钠血症、低白蛋白血症和轻度贫血。自身免疫筛查显示ANA阳性(1:80,斑点)和狼疮抗凝血,尽管可提取的核抗原为阴性。患者使用皮质类固醇和抗组胺药后病情迅速好转。结论:本病例提示潜在免疫失调患者可能存在类似毛细血管渗漏综合征的药物致全身超敏反应。意识到这种表现可能有助于早期识别和适当的免疫调节治疗,同时避免不必要的干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug-induced hypersensitivity reaction presenting as systemic capillary leak-like syndrome with polyserositis: a case report.

Background: Systemic capillary leak syndrome (SCLS) is a rare disorder characterized by increased vascular permeability leading to third-spacing of fluids and protein. Drug-induced hypersensitivity reactions can mimic SCLS clinically and radiologically.

Case presentation: A 42-year-old Vietnamese man developed abdominal distension, facial edema, and dyspnea after initiation of Helicobacter pylori eradication therapy. Imaging revealed pleural, pericardial, and peritoneal effusions, periportal edema, and interstitial pulmonary edema. Laboratory results showed hyponatremia, hypoalbuminemia, and mild anemia. Autoimmune screening revealed ANA positivity (1:80, speckled) and lupus anticoagulant, though extractable nuclear antigens were negative. The patient improved rapidly with corticosteroids and antihistamines.

Conclusion: This case suggests a probable drug-induced systemic hypersensitivity reaction mimicking capillary leak syndrome, occurring in a patient with latent immune dysregulation. Awareness of this presentation may facilitate early recognition and appropriate immunomodulatory treatment while avoiding unnecessary interventions.

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来源期刊
BMC Rheumatology
BMC Rheumatology Medicine-Rheumatology
CiteScore
3.80
自引率
0.00%
发文量
73
审稿时长
15 weeks
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