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非霍奇金淋巴瘤中的获得性血管性水肿。

Acquired angioedema in non-Hodgkin's lymphoma.

作者信息

Healy Claire, Abuzakouk Mohamed, Feighery Conleth, Flint Stephen

机构信息

Department of Oral and Maxillofacial Surgery, Oral Medicine and Oral Pathology, Dublin Dental School and Hospital, Trinity College Dublin, Dublin, Ireland.

出版信息

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007 May;103(5):e29-32. doi: 10.1016/j.tripleo.2006.11.015. Epub 2007 Feb 21.

DOI:10.1016/j.tripleo.2006.11.015
PMID:17317233
Abstract

This paper describes a middle-aged patient who developed repeated episodes of swelling of the orofacial tissues after dental treatment. On investigation, C1 inhibitor, C1q, C2, and C4 levels were all markedly reduced, and a diagnosis of acquired C1 inhibitor deficiency was made. The patient had been diagnosed with non-Hodgkin's lymphoma (NHL) 2 years previously and had undergone a successful course of chemotherapy. The development of her episodes of angioedema prompted thorough reinvestigation and a recurrence of NHL was identified. Therefore, acquired C1 inhibitor deficiency heralded a recurrence, although this had not been a manifestation when NHL was first diagnosed. The patient underwent a further course of chemotherapy and remains well, although C1 inhibitor, C1q, C2, and C4 levels remain reduced.

摘要

本文描述了一名中年患者,其在牙科治疗后出现口面部组织反复肿胀发作。经检查,C1抑制剂、C1q、C2和C4水平均显著降低,诊断为获得性C1抑制剂缺乏症。该患者2年前被诊断为非霍奇金淋巴瘤(NHL),并接受了成功的化疗疗程。她血管性水肿发作的出现促使进行了全面复查,结果发现NHL复发。因此,获得性C1抑制剂缺乏症预示着复发,尽管在首次诊断NHL时这并非其表现。患者接受了进一步的化疗疗程,目前情况良好,尽管C1抑制剂、C1q、C2和C4水平仍降低。

相似文献

1
Acquired angioedema in non-Hodgkin's lymphoma.非霍奇金淋巴瘤中的获得性血管性水肿。
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007 May;103(5):e29-32. doi: 10.1016/j.tripleo.2006.11.015. Epub 2007 Feb 21.
2
[Angioedema due to acquired complement-C1-inhibitor deficiency in a female patient with non-Hodgkin lymphoma and autoimmune hemolytic anemia].[一名患有非霍奇金淋巴瘤和自身免疫性溶血性贫血的女性患者因获得性补体C1抑制物缺乏导致血管性水肿]
Schweiz Med Wochenschr. 1991 Jun 22;121(25):943-7.
3
Angioedema due to acquired C1-inhibitor deficiency: a bridging condition between autoimmunity and lymphoproliferation.获得性C1抑制物缺乏所致血管性水肿:自身免疫与淋巴细胞增殖之间的过渡状态。
Autoimmun Rev. 2008 Dec;8(2):156-9. doi: 10.1016/j.autrev.2008.05.003. Epub 2008 Jun 12.
4
[Formation of IgG antibodies to C1 inhibitor as the cause of life-threatening angioedema].[形成针对C1抑制剂的IgG抗体作为危及生命的血管性水肿的病因]
Dtsch Med Wochenschr. 1987 Mar 27;112(13):503-6. doi: 10.1055/s-2008-1068084.
5
Acquired C1-inhibitor deficiency associated with a lupus-like anticoagulant activity.获得性C1抑制物缺乏症与狼疮抗凝物活性相关。
Ann Allergy. 1988 Nov;61(5):348-50.
6
Autoantibodies and lymphoproliferative diseases in acquired C1-inhibitor deficiencies.获得性C1抑制物缺乏症中的自身抗体与淋巴增殖性疾病。
Medicine (Baltimore). 2003 Jul;82(4):274-81. doi: 10.1097/01.md.0000085055.63483.09.
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A new type of acquired C1 inhibitor deficiency associated with systemic lupus erythematosus.一种与系统性红斑狼疮相关的新型获得性C1抑制剂缺乏症。
Arthritis Rheum. 2001 Aug;44(8):1836-40. doi: 10.1002/1529-0131(200108)44:8<1836::AID-ART321>3.0.CO;2-Y.
8
[A case of acquired angioedema].[一例获得性血管性水肿]
Ann Biol Clin (Paris). 2006 Mar-Apr;64(2):166-9.
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C1-inhibitor (C1-INH) autoantibodies in hereditary angioedema. Strong correlation with the severity of disease in C1-INH concentrate naïve patients.遗传性血管性水肿中的C1抑制因子(C1-INH)自身抗体。与未使用过C1-INH浓缩物的患者疾病严重程度密切相关。
Mol Immunol. 2007 Feb;44(6):1454-60. doi: 10.1016/j.molimm.2006.04.020. Epub 2006 Jun 5.
10
[Practical management of C1 inhibitor deficiency].[C1 抑制剂缺乏症的实际管理]
Actas Dermosifiliogr. 2007 May;98(4):240-9.

引用本文的文献

1
Clinical manifestations of hereditary angioedema and a systematic review of treatment options.遗传性血管性水肿的临床表现及治疗选择的系统评价。
Laryngoscope Investig Otolaryngol. 2021 Apr 3;6(3):394-403. doi: 10.1002/lio2.555. eCollection 2021 Jun.
2
Acquired Angioedema: A Rare Manifestation of Angioimmunoblastic T Cell Lymphoma.获得性血管性水肿:血管免疫母细胞性T细胞淋巴瘤的一种罕见表现。
Indian J Otolaryngol Head Neck Surg. 2019 Oct;71(Suppl 1):96-99. doi: 10.1007/s12070-017-1122-5. Epub 2017 Apr 7.
3
Angioedema as the first presentation of B-cell non-Hodgkin lymphoma--an unusual case with normal C1 esterase inhibitor level: a case report.
血管性水肿作为B细胞非霍奇金淋巴瘤的首发表现——1例C1酯酶抑制剂水平正常的罕见病例:病例报告
BMC Res Notes. 2014 Aug 7;7:495. doi: 10.1186/1756-0500-7-495.