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并存的韦格纳肉芽肿病和抗肾小球基底膜病。

Coexistent Wegener's granulomatosis and anti-glomerular basement membrane disease.

作者信息

Wahls T L, Bonsib S M, Schuster V L

出版信息

Hum Pathol. 1987 Feb;18(2):202-5. doi: 10.1016/s0046-8177(87)80340-4.

DOI:10.1016/s0046-8177(87)80340-4
PMID:3542802
Abstract

Wegener's granulomatosis and Goodpasture's syndrome represent two major causes of a pulmonary-renal syndrome. We describe the clinical course and morphologic features of a patient in whom pulmonary manifestations of Wegener's granulomatosis developed and were followed six months later by anti-glomerular basement membrane disease. Although we regard this as a unique and probably fortuitous association, a genetic predisposition or a secondary form of anti-GBM disease cannot be excluded.

摘要

韦格纳肉芽肿病和古德帕斯丘综合征是肺肾综合征的两大主要病因。我们描述了一名患者的临床病程和形态学特征,该患者先出现韦格纳肉芽肿病的肺部表现,六个月后又出现抗肾小球基底膜病。尽管我们认为这是一种独特且可能偶然的关联,但不能排除遗传易感性或抗肾小球基底膜病的继发形式。

相似文献

1
Coexistent Wegener's granulomatosis and anti-glomerular basement membrane disease.并存的韦格纳肉芽肿病和抗肾小球基底膜病。
Hum Pathol. 1987 Feb;18(2):202-5. doi: 10.1016/s0046-8177(87)80340-4.
2
Coexistent Wegener's granulomatosis and Goodpasture's disease: what is the mechanism?韦格纳肉芽肿病与古德帕斯彻综合征并存:其机制是什么?
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Diffuse pulmonary hemorrhage and rapidly progressive renal failure. An uncommon presentation of Wegener's granulomatosis.弥漫性肺出血和快速进展性肾衰竭。韦格纳肉芽肿的一种不常见表现。
Am J Med. 1979 May;66(5):894-8. doi: 10.1016/0002-9343(79)91149-5.
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Coexistent Wegener's granulomatosis and Goodpasture's disease.韦格纳肉芽肿病与肺出血肾炎综合征并存。
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Wegener's granulomatosis exhibiting the clinical features of Goodpasture's syndrome.表现为肺出血肾炎综合征临床特征的韦格纳肉芽肿。
Int Urol Nephrol. 1981;13(4):375-85. doi: 10.1007/BF02081939.
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POLYVASCULITIS, WITH REFERENCE TO CASES OF WEGENER'S, GOODPASTURE'S AND CEELEN'S SYNDROMES.多血管炎,参考韦格纳氏、古德帕斯彻氏和塞伦氏综合征病例
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Delayed form of Wegener's granulomatosis.韦格纳肉芽肿的迟发型
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Pulmonary renal syndromes--a review.肺肾综合征——综述
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Procalcitonin as an indicator of systemic response to infection in active pulmonary Wegener's granulomacytosis.降钙素原作为活动性肺韦格纳肉芽肿病中全身感染反应的指标。
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ACUTE PULMONARY-RENAL SYNDROMES.急性肺肾综合征
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引用本文的文献

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Anti-glomerular basement membrane disease developing 3 years after the development of Sweet syndrome and 1 year after the development of anti-neutrophil cytoplasmic antibody-associated vasculitis: a case report.抗肾小球基底膜病在Sweet 综合征发病 3 年后和抗中性粒细胞胞质抗体相关性血管炎发病 1 年后发展:病例报告。
CEN Case Rep. 2023 Aug;12(3):259-264. doi: 10.1007/s13730-022-00758-3. Epub 2022 Dec 1.
2
Sequential development of ANCA-associated vasculitis and anti-GBM disease: A report of two cases.抗中性粒细胞胞浆抗体(ANCA)相关血管炎与抗肾小球基底膜(GBM)病的序贯性发展:两例报告
Clin Case Rep. 2021 Jul 23;9(7):e04553. doi: 10.1002/ccr3.4553. eCollection 2021 Jul.
3
Asymptomatic autoantibodies associate with future anti-glomerular basement membrane disease.
无症状自身抗体与未来的抗肾小球基底膜病相关。
J Am Soc Nephrol. 2011 Oct;22(10):1946-52. doi: 10.1681/ASN.2010090928. Epub 2011 Aug 25.
4
Anti-glomerular basement membrane (anti-GBM) disease accompanied by vasculitis that was not positive for antineutrophil cytoplasmic antibodies to myeloperoxidase and proteinase 3: a report of two cases and the incidence of anti-GBM disease at one institution.抗肾小球基底膜 (anti-GBM) 病伴发血管炎,且中性粒细胞胞浆抗体(针对髓过氧化物酶和蛋白酶 3 )阴性:两例报告及一家机构的抗 GBM 病发病率。
Clin Exp Nephrol. 2011 Aug;15(4):504-13. doi: 10.1007/s10157-011-0435-z. Epub 2011 Apr 9.
5
Autoantibodies and target antigens in antineutrophil cytoplasmic antibody (ANCA)-associated vasculitides.抗中性粒细胞胞浆抗体(ANCA)相关血管炎中的自身抗体和靶抗原
Rheumatol Int. 1996;16(3):109-14. doi: 10.1007/BF01409982.
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Diverse target antigens recognized by circulating antibodies in anti-neutrophil cytoplasm antibody-associated renal vasculitides.抗中性粒细胞胞浆抗体相关性肾血管炎中循环抗体识别的多种靶抗原。
Clin Exp Immunol. 1990 Nov;82(2):238-43. doi: 10.1111/j.1365-2249.1990.tb05433.x.
7
Antineutrophil cytoplasmic antibody--a useful serological marker for vasculitis.
J Clin Immunol. 1991 Jul;11(4):161-74. doi: 10.1007/BF00917422.