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遗传性血管性水肿

Hereditary angioedema.

作者信息

Moore G P, Hurley W T, Pace S A

机构信息

Department of Emergency Medicine, Darnall Army Community Hospital, Fort Hood, Texas.

出版信息

Ann Emerg Med. 1988 Oct;17(10):1082-6. doi: 10.1016/s0196-0644(88)80450-5.

DOI:10.1016/s0196-0644(88)80450-5
PMID:3052191
Abstract

Although the condition is rare, patients with hereditary angioedema often present because of abdominal pain or airway compromise. A 27-year-old woman presented to the emergency department in acute abdominal distress. Identification of the disease in this patient allowed for proper management and avoidance of invasive procedures. Pathophysiology, clinical manifestations, diagnosis, and therapy of hereditary angioedema are discussed.

摘要

尽管这种情况很少见,但遗传性血管性水肿患者常因腹痛或气道受压而就诊。一名27岁女性因急性腹痛被送往急诊科。对该患者的疾病诊断有助于进行适当的治疗并避免侵入性操作。本文讨论了遗传性血管性水肿的病理生理学、临床表现、诊断和治疗。

相似文献

1
Hereditary angioedema.遗传性血管性水肿
Ann Emerg Med. 1988 Oct;17(10):1082-6. doi: 10.1016/s0196-0644(88)80450-5.
2
Hereditary angioneurotic edema. A case with recurring abdominal pain.遗传性血管性水肿。一例反复腹痛的病例。
Am J Dig Dis. 1972 May;17(5):435-8. doi: 10.1007/BF02231296.
3
[Abdominal manifestations in hereditary acute angioneurotic oedema. Value of study of the complement system (author's transl)].[遗传性急性血管神经性水肿的腹部表现。补体系统研究的价值(作者译)]
Nouv Presse Med. 1977 Jun 18;6(25):2233, 2235-8.
4
CT findings in small bowel angioedema: a cause of acute abdominal pain.小肠血管性水肿的CT表现:急性腹痛的一个病因
Emerg Radiol. 2007 Feb;13(5):281-3. doi: 10.1007/s10140-006-0562-0. Epub 2007 Jan 10.
5
[Hereditary angioneurotic edema. Clinical aspects and extended diagnostic and therapeutic possibilities].[遗传性血管性水肿。临床特征及扩展的诊断与治疗可能性]
Dtsch Med Wochenschr. 1979 Mar 16;104(11):405-9. doi: 10.1055/s-0028-1103919.
6
[Familial angioneurotic edema: a case with typical abdominal and respiratory complications].[家族性血管性水肿:一例伴有典型腹部和呼吸系统并发症的病例]
Schweiz Med Wochenschr. 1970 Aug 29;100(35):1491-3.
7
Recurrent abdominal pain due to hereditary angioedema.
Indian J Pediatr. 2007 Jan;74(1):83-4. doi: 10.1007/s12098-007-0034-x.
8
[Hereditary angioedema. A rare cause of acute abdominal pain with ascites].[遗传性血管性水肿。伴有腹水的急性腹痛的罕见病因]
Dtsch Med Wochenschr. 1998 Oct 2;123(40):1166-71. doi: 10.1055/s-2007-1024139.
9
Acute abdominal attack of hereditary angioneurotic oedema associated with ultrasound abnormalities suggestive of acute hepatitis.遗传性血管性水肿急性腹部发作伴超声异常,提示急性肝炎。
Acta Paediatr. 2002;91(8):971-4. doi: 10.1080/080352502760148720.
10
Hereditary angioneurotic oedema: an unusual cause of recurring abdominal pain.遗传性血管性水肿:反复腹痛的罕见病因。
Gut. 1970 Dec;11(12):983-8. doi: 10.1136/gut.11.12.983.

引用本文的文献

1
Clinical features of hereditary angioedema and warning signs (H4AE) for its identification.遗传性血管性水肿的临床特征和识别警示(H4AE)。
Clinics (Sao Paulo). 2022 Mar 19;77:100023. doi: 10.1016/j.clinsp.2022.100023. eCollection 2022.
2
Characterizing disease manifestations and treatment outcomes among patients with orofacial granulomatosis in China.中国口腔面部肉芽肿病患者的疾病表现及治疗结果特征分析。
JAAD Int. 2020 Aug 12;1(2):126-134. doi: 10.1016/j.jdin.2020.07.003. eCollection 2020 Dec.
3
Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis.
巴西遗传性血管性水肿管理指南 - 2017年更新 第1部分:定义、分类与诊断
Clinics (Sao Paulo). 2018;73:e310. doi: 10.6061/clinics/2018/e310. Epub 2018 May 3.
4
Hereditary angioedema caused by c1-esterase inhibitor deficiency: a literature-based analysis and clinical commentary on prophylaxis treatment strategies.遗传性血管性水肿致 C1 酯酶抑制剂缺乏症:基于文献的分析和预防治疗策略的临床评论。
World Allergy Organ J. 2011 Feb;4(2 Suppl):S9-S21. doi: 10.1097/WOX.0b013e31821359a2.
5
Brazilian guidelines for the diagnosis and treatment of hereditary angioedema.巴西遗传性血管性水肿诊断和治疗指南。
Clinics (Sao Paulo). 2011;66(9):1627-36. doi: 10.1590/s1807-59322011000900021.
6
Hereditary angioedema: New therapeutic options for a potentially deadly disorder.遗传性血管性水肿:一种潜在致命疾病的新治疗选择。
BMC Blood Disord. 2010 May 14;10:3. doi: 10.1186/1471-2326-10-3.
7
C1 inhibitor deficiency: consensus document.C1 抑制剂缺乏症:共识文件。
Clin Exp Immunol. 2005 Mar;139(3):379-94. doi: 10.1111/j.1365-2249.2005.02726.x.
8
Current management of hereditary angio-oedema (C'1 esterase inhibitor deficiency).遗传性血管性水肿(C1酯酶抑制剂缺乏症)的当前管理
J Clin Pathol. 2002 Apr;55(4):266-70. doi: 10.1136/jcp.55.4.266.
9
Hereditary angioedema: an unusual case in an African-American woman.遗传性血管性水肿:一名非裔美国女性的罕见病例。
J Natl Med Assoc. 1998 Feb;90(2):115-8.