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血管性水肿作为系统性红斑狼疮的首发特征。

Angioedema as the presenting feature of systemic lupus erythematosus.

作者信息

Kumar Naveen, Surendran Deepanjali, Bammigatti Chanaveerappa

机构信息

Department of Medicine, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry, India.

出版信息

BMJ Case Rep. 2018 Mar 28;2018:bcr-2018-224222. doi: 10.1136/bcr-2018-224222.

DOI:10.1136/bcr-2018-224222
PMID:29593002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5878267/
Abstract

A young female in her early 20s presented with low-grade fever for 1 month, puffiness of face and abdominal distension for 15 days. Evaluation revealed pancytopenia with normocellular marrow, hypocomplementaemia and Coomb's positive haemolytic anaemia. She had angioedema with laryngospasm and worsening facial oedema which had dramatic response to steroids. Further workup lead to a diagnosis of systemic lupus erythematosus with neuropsychiatric involvement. Treatment with pulse steroids and cyclophosphamide resulted in dramatic improvement of her symptoms with no recurrence of angioedema during her follow-up visits.

摘要

一名20岁出头的年轻女性出现低热1个月,面部肿胀和腹胀15天。检查发现全血细胞减少伴正常细胞骨髓、低补体血症和库姆斯试验阳性的溶血性贫血。她有血管性水肿伴喉痉挛,面部水肿加重,对类固醇有显著反应。进一步检查诊断为系统性红斑狼疮伴神经精神系统受累。脉冲类固醇和环磷酰胺治疗使她的症状显著改善,随访期间血管性水肿未复发。

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本文引用的文献

1
Refractory Angioedema in a Patient with Systemic Lupus Erythematosus.一名系统性红斑狼疮患者的难治性血管性水肿
Iran J Med Sci. 2015 Jul;40(4):372-5.
2
Facial angioedema and systemic lupus erythematosus: case report.
J Oral Maxillofac Surg. 2015 May;73(5):928-32. doi: 10.1016/j.joms.2014.12.007. Epub 2014 Dec 13.
3
Derivation and validation of the Systemic Lupus International Collaborating Clinics classification criteria for systemic lupus erythematosus.系统性红斑狼疮国际协作临床分类标准的推导与验证
Arthritis Rheum. 2012 Aug;64(8):2677-86. doi: 10.1002/art.34473.
4
Intractable acquired autoimmune angioedema in a patient with systemic lupus erythematosus.一名系统性红斑狼疮患者的难治性获得性自身免疫性血管性水肿
Rev Bras Reumatol. 2010 Jan-Feb;50(1):102-6.
5
Angioedema and systemic lupus erythematosus--a complementary association?血管性水肿与系统性红斑狼疮——一种互补性关联?
Ann Acad Med Singap. 2007 Feb;36(2):142-5.
6
Acquired C1-inhibitor deficiency in a patient with systemic lupus erythematosus: a case report and review of the literature.系统性红斑狼疮患者获得性C1抑制剂缺乏症:一例病例报告及文献复习
Eur J Clin Invest. 2005 Dec;35(12):781-4. doi: 10.1111/j.1365-2362.2005.01571.x.
7
Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary Angioedema.2003年加拿大遗传性血管性水肿诊断、治疗及管理国际共识算法
J Allergy Clin Immunol. 2004 Sep;114(3):629-37. doi: 10.1016/j.jaci.2004.06.043.
8
Hereditary and acquired angioedema: problems and progress: proceedings of the third C1 esterase inhibitor deficiency workshop and beyond.遗传性和获得性血管性水肿:问题与进展:第三届C1酯酶抑制剂缺乏症研讨会及后续会议论文集
J Allergy Clin Immunol. 2004 Sep;114(3 Suppl):S51-131. doi: 10.1016/j.jaci.2004.06.047.
9
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Medicine (Baltimore). 2003 Jul;82(4):274-81. doi: 10.1097/01.md.0000085055.63483.09.
10
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