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Bayrashevskaya A.V.

I.M. Sechenov First Moscow State Medical University of the Ministry of Health of Russia

Degtyareva N.D.

I.M. Sechenov First Moscow State Medical University of the Ministry of Health of Russia

Radenska-Lopovok S.G.

I.M. Sechenov First Moscow State Medical University

ANCA-associated small-vessel vasculitides

Authors:

Bayrashevskaya A.V., Degtyareva N.D., Radenska-Lopovok S.G.

More about the authors

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To cite this article:

Bayrashevskaya AV, Degtyareva ND, Radenska-Lopovok SG. ANCA-associated small-vessel vasculitides. Russian Journal of Archive of Pathology. 2022;84(1):50‑58. (In Russ.)
https://doi.org/10.17116/patol20228401150

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References:

  1. Jenntte JC. Overview of the 2012 revised International Chapel Hill Consensus Conference nomenclature of vasculitides. J Clin ExpNephrol. 2012;17(5):603-606.  https://doi.org/10.1007/s10157-013-0869-6
  2. Kronbichler A, Lee KH, Denicolò S, Choi D, Lee H, Ahn D, Kim KH, Lee JH, Kim H, Hwang M, Jung SW, Lee C, Lee H, Sung H, Lee D, Hwang J, Kim S, Hwang I, Kim DY, Kim HJ, Cho G, Cho Y, Kim D, Choi M, Park J, Park J, Tizaoui K, Li H, Smith L, Koyanagi A, Jacob L, GauckierPh, Shin JI. Immunopathogenesis of ANCA-associated vasculitis. Int J Mol Sci. 2020;21(19):7319. https://doi.org/10.3390/ijms21197319
  3. Kitching AR, Anders HJ, BasuN, Brouwer E, Gordon J, Jayne DR, Kullman J, Lyons PA, Merke lPA, Savage COS, Specks U, Kain R. ANCA-associated vasculitis. Nat Rev Dis Primers. 2020;6(1):71.  https://doi.org/10.1038/s41572-020-0204-y
  4. Bradwell RP, Mead AR, Stokes GP. Advanced atlas of autoantibody patterns. Birmingham: The Binding Site; 1999.
  5. Almaani S, Fussner LA, Brodsky S, Meara AS, Jayne D. ANCA-associated vasculitis: an update. J Clin Med. 2021;10(7):1446. https://doi.org/10.3390/jcm10071446
  6. Michailidou D, Mustelin T, Lood C. Role of neutrophils in systemic vasculitides. Front Immunol. 2020;11:619705. https://doi.org/10.3389/fimmu.2020.619705
  7. Geetha D, Jefferson JA. ANCA-associated vasculitis: core curriculum 2020. Am J Kidney Dis. 2020;75(1):124-137.  https://doi.org/10.1053/j.ajkd.2019.04.031
  8. Klose CSN, Artis D. Innate lymphoid cells control signaling circuits to regulate tissue-specific immunity. Cell Res. 2020;30(6):475-491.  https://doi.org/10.1038/s41422-020-0323-8
  9. Morita H, Moro K, Koyasu S. Innate lymphoid cells in allergic and nonallergic inflammation. J Allergy Clin Immunol. 2016; 138(5):1253-1264. https://doi.org/10.1016/j.jaci.2016.09.011
  10. Vaglio A, Buzio C, Zwerina J. Eosinophilic granulomatosis with polyangiitis (Churg—Strauss): state of the art. Allergy. 2013;68(3):261-273.  https://doi.org/10.1111/all.12088
  11. Zwerina J, Bach C, Martorana D, Jatzwauk M, Hegasy G, Moosig F, Bremer J, Wieczorek St, Moschen A, Tilg H, Neumann Th, Spreewald BM, Schett G, Vaglio A. Eotaxin-3 in Churg—Strauss syndrome: a clinical and immunogenetic study. Rheumatology (Oxford). 2011;50(10):1823-1827. https://doi.org/10.1093/rheumatology/keq445
  12. Jakiela B, Szczeklik W, Plutecka H, Sokolowska B, Mastalerz L, Sanak M, Bazan-Socha S, Szczeklik A, Musial J. Increased production of IL-5 and dominant Th2-type response in airways of Churg—Strauss syndrome patients. Rheumatology (Oxford). 2012; 51(10):1887-1893. https://doi.org/10.1093/rheumatology/kes171
  13. Pacholczak R, Bazan-Socha S, Iwaniec T, Zaręba L, Kielczewski S, Walocha JA, Musiał J, Dropiński J. Endothelial dysfunction in patients with eosinophilic granulomatosis with polyangiitis. Clin Rheumatol. 2019;38(2):417-424.  https://doi.org/10.1007/s10067-018-4253-5
  14. Klinger H. Grenzformen der periarteritisnodosa. Z Pathol. 1931; 42:455-480. 
  15. Wegener F. Über eine eigenartige rhinogene Granulomatose mit besonderer Beteilgung des Arteriensystems und der Nieren. Beitr Path Anat. 1939;102:36-38. 
  16. Kubaisi B, Abu Samra K, Foster CS. Granulomatosis with polyangiitis (Wegener’s disease): An updated review of ocular disease manifestations. Intractable Rare Dis Res. 2016;5(2):61-69.  https://doi.org/10.5582/irdr.2016.01014
  17. https://dep_pediatr.pnzgu.ru/files/dep_pediatr.pnzgu.ru/granulematoz_vegenera.pdf  https://dep_pediatr.pnzgu.ru/files/dep_pediatr.pnzgu.ru/granulematoz_vegenera.pdf
  18. Baranov AA, Alexeeva EI, eds. Detskaya revmatologiya. Atlas. 2nd ed. M.: Pediatr; 2015. (In Russ).
  19. Nakazawa D, Masuda S, Tomaru U, Ishizu A. Pathogenesis and therapeutic interventions for ANCA-associated vasculitis. Nat Rev Rheumatol. 2019;15(2):91-101.  https://doi.org/10.1038/s41584-018-0145-y
  20. Masiak A, Zdrojewski Z, Pęksa R, Smoleńska Ż, Czuszyńska Z, Siemińska A, Kowalska B, Stankiewicz C, Rutkowski B, Bułło-Piontecka B. The usefulness of histopathological examinations of non-renal biopsies in the diagnosis of granulomatosis with polyangiitis. Reumatologia. 2017;55(5):230-236.  https://doi.org/10.5114/reum.2017.71638
  21. Wojciechowska J, KręCicki T. Clinical characteristics of patients with granulomatosis with polyangiitis and microscopic polyangiitis in ENT practice: a comparative analysis. Acta Otorhinolaryngol Ital. 2018;38(6):517-527.  https://doi.org/10.14639/0392-100X-1776
  22. Greco A, Marinelli C, Fusconi M, Macri GF, Gallo A, De Virgilio A, Zambetti G, de Vincentiis M. Clinic manifestations in granulomatosis with polyangiitis. Int J Immunopathol Pharmaco. 2016;29(2):151-159.  https://doi.org/10.1177/0394632015617063
  23. Peters JE, Gupta V, Saeed IT, Offiah C, Jawad ASM. Severe localised granulomatosis with polyangiitis (Wegener’s granulomatosis) manifesting with extensive cranial nerve palsies and cranial diabetes insipidus: a case report and literature review. BMC Neurol. 2018;18:59.  https://doi.org/10.1186/s12883-018-1058-8
  24. Jennette JC, Nachman PH. ANCA glomerulonephritis and vasculitis. CJASN Clin J Am Soc Nephr. 2017;12(10):1680-1691. https://doi.org/10.2215/CJN.02500317
  25. Perry SR, Rootman J, White VA. The clinical and pathologic constellation of Wegener granulomatosis of the orbit. Ophthalmology. 1997;104(4):683-694.  https://doi.org/10.1016/s0161-6420(97)30251-6
  26. Kędzierska K, Sindrewicz K, Smektała T, Wiśniewska M, Masiuk M, Staniszewska E, Sporniak-Tutak K, Gołembiewska E, Ciechanowski K. Wegener’s granulomatosis and pyoderma gangrenosum-rare causes of facial ulcerations. Postepy Hig Med Dosw (Online). Postepy Hig Med Dosw. (Online). 2016;70:210-218.  https://doi.org/10.5604/17322693.1197372
  27. Pan SW, Wang C, Zhang X, Zhang L, Yan QQ, Zhao CJ, Chang C, Luan XD. A rare endoscopic appearance of granulomatosis with polyangiitis involving the intestine: a case report. BMC Gastroenterology. 2018;18(1):154.  https://doi.org/10.1186/s12876-018-0885-9
  28. Pagnoux C, Mahr A, Cohen P, Guillevin L. Presentation and outcome of gastrointestinal involvement in systemic necrotizing vasculitides. Medicine Baltimore. 2005;84(2):115-128.  https://doi.org/10.1097/01.md.0000158825.87055.0b
  29. De Oliveira NC, David TE, Armstrong S, Ivanov J. Aortic and mitral valve replacement with reconstruction of the intervalvular fibrous body: an analysis of clinical outcomes. J Thorac Cardiovasc Surg. 2005;129(2):286-290.  https://doi.org/10.1016/j.jtcvs.2004.09.032
  30. Raghunathan V, Pelcovits A, Gutman D, Carino G. Cardiogenic shock from coronary vasculitis in granulomatosis with polyangiitis. BMJ Case Rep. 2017:bcr2017220233. https://doi.org/10.1136/bcr-2017-220233
  31. Churg J, Strauss L. Allergic granulomatosis, allergic angiitis, and periarteritis nodosa. Am J Pathol. 1951;27:277-301. 
  32. Furuta S, Iwamoto T, Nakajima H. Update on eosinophilic granulomatosis with polyangiitis. Allergol Int. 2019;68(4):430-436.  https://doi.org/10.1016/j.alit.2019.06.004
  33. Voitsekhovskii VV, Pogrebnaya MV, Goborov ND, Fomina OP, Goryacheva SA. Peculiarities of diagnosis and treatment of Churg-Strauss syndrome. Bulletin of Physiology and Pathology of Respiration=Byulleten’ fiziologii i patologii dykhaniya. 2017;64:79-87. (In Russ.). https://doi.org/10.12737/article_59361a30e7f1e7.92279749
  34. Gioffredi A, Maritati F, Oliva E, Buzio C. Eosinophilic granulomatosis with polyangiitis: an overview. Front Immunol. 2014;5:549.  https://doi.org/10.3389/fimmu.2014.00549
  35. Ishibashi M, Kawahara Y, Chen KR. Spectrum of cutaneous vasculitis in eosinophilic granulomatosis with polyangiitis (Churg-Strauss): a case series. Am J Dermatopathol. 2015;37(3):214-221.  https://doi.org/10.1097/dad.0000000000000192
  36. Kataoka H, Tomita T, Kondo M, Mukai M. Presence of purpura is related to active inflammation in association with IL-5 in eosinophilic granulomatosis with polyangiitis. Rheumatol Int. 2021;41(2):449-454.  https://doi.org/10.1007/s00296-020-04672-8
  37. Zhou L, Cao F, Fan S, Chen P, Ding S, Liu G, Ouyang R. A case of eosinophilic granulomatosis with polyangiitis complicated with a similar condition to IgG4 related lung disease. BMC Pulm Med. 2019;19(1):154.  https://doi.org/10.1186/s12890-019-0917-4
  38. Comarmond C, Pagnoux C, Khellaf M, Cordier JF, Hamidou M, Viallard JF, Maurier F, et al. Eosinophilic granulomatosis with polyangiitis (Churg-Strauss): clinical characteristics and long-term follow up of the 383 patients enrolled in the French Vasculitis Study Group cohort. Arthritis Rheum. 2013;65(1):270-281.  https://doi.org/10.1002/art.37721
  39. Pinckard JK. A case of granulomatosis with polyangiitis diagnosed at autopsy. Acad Forensic Pathol. 2017;7(2):288-298.  https://doi.org/10.23907/2017.026
  40. Sheikh H, Siddiqui M, Uddin S, Haq A, Yaqoob U. The clinicopathological profile of eosinophilic myocarditis. Cureus. 2018; 10(12):e3677. https://doi.org/10.7759/cureus.3677
  41. Franco DL, Ruff K, Mertz L, Lam-Himlin DM, Heigh R. Eosinophilic granulomatosis with polyangiitis and diffuse gastrointestinal involvement. Case Rep Gastroenterol. 2014;8(3):329-336.  https://doi.org/10.1159/000369129
  42. Li D, Shi C, Ding Z, Li X. Budd-Chiari syndrome as a complication of eosinophilic granulomatosis with polyangiitis in a young Chinese man: a case report. J Int Med Res. 2020;48(10):300060520964352. https://doi.org/10.1177/0300060520964352
  43. Calatroni M, Oliva E, Gianfreda D, Gregorini G, Allinov M, Ramirez GA, Bozzolo EP, Monti S, Bracaglia C, Marucci G, Bodria M, Sinico RA, Pieruzzi F, Moroni G, Pastore S, Emmi G, Esposito P, Catanoso M, Barbano G, Bonanni A, Vaglio A. ANCA-associated vasculitis in childhood: recent advances. Italian J Ped. 2017;43(1):46.  https://doi.org/10.1186/s13052-017-0364-x

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