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本文引用的文献

1
High prevalence of splenic marginal zone lymphoma among patients with acquired C1 inhibitor deficiency.获得性C1抑制剂缺乏患者中脾边缘区淋巴瘤的高患病率。
Br J Haematol. 2016 Mar;172(6):902-8. doi: 10.1111/bjh.13908. Epub 2016 Jan 5.
2
Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group.血管性水肿的分类、诊断和治疗方法：遗传性血管性水肿国际工作组的共识报告。
Allergy. 2014 May;69(5):602-16. doi: 10.1111/all.12380. Epub 2014 Mar 27.
3
Gastrointestinal manifestations, diagnosis, and management of hereditary angioedema.遗传性血管性水肿的胃肠道表现、诊断和治疗。
J Clin Gastroenterol. 2013 Nov-Dec;47(10):817-23. doi: 10.1097/MCG.0b013e31829e7edf.
4
Diagnosis and management of angioedema with abdominal involvement: a gastroenterology perspective.伴有腹部受累的血管性水肿的诊断和治疗：胃肠病学视角。
World J Gastroenterol. 2010 Oct 21;16(39):4913-21. doi: 10.3748/wjg.v16.i39.4913.
5
Acquired deficiency of the inhibitor of the first complement component: presentation, diagnosis, course, and conventional management.获得性第一补体成分抑制物缺乏症：临床表现、诊断、病程及传统治疗
Immunol Allergy Clin North Am. 2006 Nov;26(4):669-90. doi: 10.1016/j.iac.2006.08.002.
6
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.
7
CT of angioedema of the small bowel.小肠血管性水肿的CT检查
AJR Am J Roentgenol. 2001 Mar;176(3):649-52. doi: 10.2214/ajr.176.3.1760649.

由后天性C1酯酶抑制剂缺乏引起的肠道血管性水肿，与潜在的脾边缘区淋巴瘤相关。

Intestinal angioedema caused by an acquired C1 esterase inhibitor deficiency associated with underlying splenic marginal zone lymphoma.

作者信息

Thongtan Thanita, Deb Anasua, Bedanie Genanew, Elmassry Mohamed, Soape Matthew, Nugent Kenneth

机构信息

Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas.

出版信息

Proc (Bayl Univ Med Cent). 2021 Feb 22;34(4):519-520. doi: 10.1080/08998280.2021.1885277.

DOI:10.1080/08998280.2021.1885277
PMID:34219945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8224193/
Abstract

A 75-year-old woman presented with recurrent abdominal pain and vomiting for 1 year and was later found to have splenomegaly and pancytopenia. This case report depicts a clinical picture of intestinal angioedema, a challenging diagnosis, and an underlying rare syndrome of acquired C1 esterase inhibitor deficiency associated with splenic marginal zone lymphoma.

摘要

一名75岁女性因反复腹痛和呕吐1年就诊，后来发现有脾肿大和全血细胞减少。本病例报告描述了肠道血管性水肿的临床表现、具有挑战性的诊断以及与脾边缘区淋巴瘤相关的罕见的获得性C1酯酶抑制剂缺乏综合征。