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I型遗传性血管性水肿患者孕期前后血管性水肿发作频率的比较

Comparison of the Frequency of Angioedema Attack, before and during Pregnancy, in a Patient with Type I Hereditary Angioedema.

作者信息

Satomura Atsushi, Fujita Takayuki, Nakayama Tomohiro

机构信息

Division of Laboratory Medicine, Department of Pathology and Microbiology, Nihon University School of Medicine, Japan.

Division of Nephrology, Hypertension and Endocrinology, Department of Medicine, Nihon University School of Medicine, Japan.

出版信息

Intern Med. 2018 Mar 1;57(5):751-755. doi: 10.2169/internalmedicine.9407-17. Epub 2017 Nov 1.

DOI:10.2169/internalmedicine.9407-17
PMID:29093422
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5874354/
Abstract

The patient was a 38-year-old Japanese woman who had been diagnosed with hereditary angioedema type I at 7 years of age based on her family history. She had undergone four pregnancies. She gave birth to a healthy baby girl after her first pregnancy and had reported few episodes of angioedema. However, she subsequently required abortions due to frequent angioedema episodes that occurred during her three subsequent pregnancies. Thus, our patient showed two clinical pregnancy courses. After treating her with C1-inhibitor concentrate, her symptoms of angioedema disappeared. The preventive use of C1 inhibitor concentrates should be considered in hereditary angioedema (HAE) patients with frequent angioedema attacks during pregnancy.

摘要

该患者是一名38岁的日本女性,根据家族病史,她在7岁时被诊断为I型遗传性血管性水肿。她经历过四次怀孕。第一次怀孕后生下了一个健康的女婴,且报告的血管性水肿发作次数很少。然而,在随后的三次怀孕中,由于频繁出现血管性水肿发作,她随后需要进行流产。因此,我们的患者表现出两种临床妊娠过程。用C1抑制剂浓缩物治疗后,她的血管性水肿症状消失了。对于在怀孕期间频繁出现血管性水肿发作的遗传性血管性水肿(HAE)患者,应考虑预防性使用C1抑制剂浓缩物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e500/5874354/1dc2a27e6a57/1349-7235-57-0751-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e500/5874354/d1239a5eb179/1349-7235-57-0751-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e500/5874354/1dc2a27e6a57/1349-7235-57-0751-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e500/5874354/d1239a5eb179/1349-7235-57-0751-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e500/5874354/1dc2a27e6a57/1349-7235-57-0751-g002.jpg

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本文引用的文献

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High attack frequency in patients with angioedema due to C1-inhibitor deficiency is a major determinant in switching to home therapy: a real-life observational study.C1抑制剂缺乏所致血管性水肿患者的高发作频率是转向家庭治疗的主要决定因素:一项真实世界观察性研究
Orphanet J Rare Dis. 2016 Sep 29;11(1):133. doi: 10.1186/s13023-016-0518-8.
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Management of Pregnancy and Delivery in Patients With Hereditary Angioedema Due to C1 Inhibitor Deficiency.遗传性血管性水肿患者妊娠和分娩的管理:C1 抑制剂缺乏症。
J Investig Allergol Clin Immunol. 2016;26(3):161-7. doi: 10.18176/jiaci.0037.
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Diagnosis and treatment of bradykinin-mediated angioedema: outcomes from an angioedema expert consensus meeting.
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Current status of implementation of self-administration training in various regions of Europe, Canada and the USA in the management of hereditary angioedema.欧洲、加拿大和美国各地区在遗传性血管性水肿管理中实施自我管理培训的现状。
Int Arch Allergy Immunol. 2013;161 Suppl 1:10-6. doi: 10.1159/000351233. Epub 2013 May 28.
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Hereditary angioedema attacks resolve faster and are shorter after early icatibant treatment.遗传性血管性水肿发作经早期艾卡替班特治疗后缓解更快、持续时间更短。
PLoS One. 2013;8(2):e53773. doi: 10.1371/journal.pone.0053773. Epub 2013 Feb 4.
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WAO Guideline for the Management of Hereditary Angioedema.WAO 遗传性血管性水肿管理指南。
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Guideline for hereditary angioedema (HAE) 2010 by the Japanese Association for Complement Research - secondary publication.日本补体研究协会 2010 年遗传性血管性水肿指南 - 二次出版物。
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