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以腹膜炎为首发表现的系统性红斑狼疮:一例报告。

Peritonitis as the first presentation of systemic lupus erythematous: a case report.

机构信息

Baharloo Hospital, Tehran University of Medical Sciences (TUMS), Tehran, Iran.

Department of Gastroenterology, Tehran University of Medical Sciences (TUMS), Tehran, Iran.

出版信息

J Med Case Rep. 2021 Dec 26;15(1):611. doi: 10.1186/s13256-021-03216-3.

DOI:10.1186/s13256-021-03216-3
PMID:34953487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8710242/
Abstract

BACKGROUND

Systemic lupus erythematosus is an inflammatory disease affecting several organs. Serositis is one of the systemic lupus erythematosus presentations, but peritonitis is a relatively rare presentation. Particularly, it is extremely rare to observe peritonitis as the first presentation of systemic lupus erythematosus.

CASE PRESENTATION

Here, we present a case of peritonitis without other symptoms of systemic lupus erythematosus, in a patient who was finally diagnosed with systemic lupus erythematosus. Our patient was a 27-year-old Persian/Caucasian male with fatigue, weakness, weight loss, abdominal distension, massive ascites, and normocytic hemolytic anemia. He did not mention any prior medical conditions and did not use any drugs. There were no signs of thyroid dysfunction, cardiac dysfunction, cancers, infectious diseases, hepatitis, kidney diseases, or other diseases. Low-gradient, high-protein ascites fluid, and positive antinuclear antibody and anti-double stranded DNA were in favor of systemic lupus erythematosus. Corticosteroid pulse therapy led to resolution of ascites, and the patient was discharged with prednisolone and hydroxychloroquine.

CONCLUSION

Peritonitis is a rare presentation of systemic lupus erythematosus, particularly as the first presentation and in the absence of other signs and symptoms; however, systemic lupus erythematosus should be considered as one the differential diagnoses for peritonitis when other etiologies have been ruled out.

摘要

背景

系统性红斑狼疮是一种影响多个器官的炎症性疾病。浆膜炎是系统性红斑狼疮的一种表现,但腹膜炎是相对罕见的表现。特别是,观察到腹膜炎作为系统性红斑狼疮的首发表现是极其罕见的。

病例介绍

在这里,我们报告了一例无系统性红斑狼疮其他症状的腹膜炎患者,该患者最终被诊断为系统性红斑狼疮。我们的患者是一名 27 岁的波斯/高加索男性,表现为疲劳、虚弱、体重减轻、腹胀、大量腹水和正细胞正色素性溶血性贫血。他没有提到任何既往病史,也没有使用任何药物。没有甲状腺功能障碍、心脏功能障碍、癌症、传染病、肝炎、肾脏疾病或其他疾病的迹象。低梯度高蛋白腹水、抗核抗体和抗双链 DNA 阳性均支持系统性红斑狼疮的诊断。皮质类固醇脉冲治疗导致腹水消退,患者出院时给予泼尼松龙和羟氯喹。

结论

腹膜炎是系统性红斑狼疮的一种罕见表现,特别是作为首发表现且无其他体征和症状时;然而,当排除其他病因后,应将系统性红斑狼疮作为腹膜炎的鉴别诊断之一。

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本文引用的文献

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A comparison of the performance of the 2019 European League Against Rheumatism/American College of Rheumatology criteria and the 2012 Systemic Lupus International Collaborating Clinics criteria with the 1997 American College of Rheumatology classification criteria for systemic lupus erythematous in new-onset Chinese patients.2019年欧洲抗风湿病联盟/美国风湿病学会标准与2012年系统性红斑狼疮国际协作临床组标准在初发中国患者中与1997年美国风湿病学会系统性红斑狼疮分类标准的性能比较。
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The diagnostic accuracies of the 2012 SLICC criteria and the proposed EULAR/ACR criteria for systemic lupus erythematosus classification are comparable.2012 年 SLICC 标准和建议的 EULAR/ACR 标准对系统性红斑狼疮分类的诊断准确性相当。
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Systemic Lupus Erythematosus Presenting with Massive Ascites: A Case of Pseudo-Pseudo Meigs Syndrome.以大量腹水为表现的系统性红斑狼疮:一例假性梅格斯综合征病例
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Chinese SLE Treatment and Research group (CSTAR) registry VII: prevalence and clinical significance of serositis in Chinese patients with systemic lupus erythematosus.中国系统性红斑狼疮治疗与研究协作组(CSTAR)注册研究VII:中国系统性红斑狼疮患者浆膜炎的患病率及临床意义
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Ascites due to lupus peritonitis: a rare form of onset of systemic lupus erythematosus.狼疮性腹膜炎所致腹水:系统性红斑狼疮的一种罕见起病形式。
Rev Bras Reumatol. 2012 Jan-Feb;52(1):116-9.
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Pathogenesis of systemic lupus erythematosus revisited 2011: end organ resistance to damage, autoantibody initiation and diversification, and HLA-DR.2011 年系统性红斑狼疮发病机制的再探讨:靶器官对损伤的抵抗、自身抗体的起始和多样化,以及 HLA-DR。
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Ascites: diagnosis and management.腹水:诊断与管理
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Systemic lupus erythematosus.系统性红斑狼疮
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