Vasculitis from the Perspective of a Dermatologist

1.    AGUR, T., LEVY, Y., PLOTKIN, E. et al. Minocycline-induced polyarteritis nodosa-like vasculitis. Israel Medical Association Journal, 2014, 16(5), p. 322–323.

2.   ALFREDO, C. S., NUNES, N. A., LEN, C. A. et al., Henoch-Schönlein purpura: Recurrence and chronicity. J. Pediatr. (Rio. J)., 2007, 83(2), p. 177–180.

3.    ALIBAZ-ONER, F., SAWALHA, A. H., DIRESKENELI, H. Management of Behçet’s disease. Current Opinion in Rheumatology, 2018, 30(3), p. 238–242.

4.   ALIBAZ-ONER, F., KOSTER, M. J., CROWSON, C. S. et al. Clinical Spectrum of Medium-Sized Ves-sel Vasculitis. Arthritis Care Res., 2017, 69(6), p. 884–891.

5.    ALPSOY, E. Behçet’s disease: A comprehensive review with a focus on epidemiology, etiology and clinical features, and management of mucocutaneous lesions. Journal of Dermatology, 2016, 43(6), p. 620–632.

6.    ARORA, A., WETTER, D. A., GONZALEZ-SANTIAGO, T. M. et al. Incidence of leukocytoclastic vasculitis, 1996 to 2010: A population-based study in olm-sted county, Minnesota. Mayo Clin. Proc., 2014, 89(11), p. 1515–1524.

7.    AWAN, S., MANDHADI, R., ABELES, A. M. Refractory psoriatic arthritis and polyarteritis nodosa: Co-occurrence in a patient with undiagnosed HIV. Conn. Med., 2017, 41(5), p. 285–289.

8.    BARRA, L., YANG, G., PAGNOUX, C. Non-glucocorticoid drugs for the treatment of Takayasu’s arteritis: A systematic review and meta-analysis. Autoimmunity Reviews, 2018, 17(7), p. 683–693.

9.   BLANCO, R., MARTÍNEZ-TABOADA, V. M., RODRÍGUEZ-VALVERDE, V. et al. Henoch-Schonlein purpura in adulthood and childhood: Two different expressions of the same syndrome. Arthritis Rheum., 1997, 40(5), p. 859–864.

10. BOOTH, A., HARPER, L., HAMMAD, T. et al. Prospective Study of TNFα Blockade with Infliximab in Anti-Neutrophil Cytoplasmic Antibody-Associated Systemic Vasculitis. J. Am. Soc. Nephrol., 2004, 15(3), p. 717–721.

11. BOSCO, L., PERONI, A., SCHENA, D. et al. Cutaneous manifestations of Churg-Strauss syndrome: Report of two cases and review of the literature. Clin. Rheumatol., 2011, 30(4), p. 573–580.

12. BOSCH, X., GUILABERT, A., ESPINOSA, G. et al. Treatment of antineutrophil cytoplasmic antibody-associated vasculitis: A systematic review. JAMA, 2007, 298(6), p. 655–669.

13. BORGES, A. S., BRASILEIRO, A., APETATO, M. Nodular vasculitis associated with lung adenocarcinoma. Anais Brasileiros de Dermatologia, 2018, 93(6), p. 887–889.

14. BORCHERS, A. T., GERSHWIN, M. E. Giant cell arteritis: A review of classification, pathophysiology, geoepidemiology and treatment. Autoimmunity Reviews, 2012, 11(6–7).

15. BREUER, G. S., REINUS, K., NESHER, G. et al. Recur-rent unilateral orchitis as a presenting symptom of polyarteritis nodosa. Isr. Med. Assoc. J., 2015, 17(9), p. 585–586.

16. BROGAN, P., ELEFTHERIOU, D. Vasculitis update: pathogenesis and biomarkers. Pediatric Nephrology, 2018, 33(2), p. 187–198.

17. BRUCATO, A., MAESTRONI, S., MASCIOCCO, G. et al. Il coinvolgimento cardiaco nella sindrome di Churg-Strauss. G. Ital. Cardiol., 2015, 16(9), p. 493–500.

18. CABRAL, D. A., URIBE, A. G., BENSELER, S. et al. Classification, presentation, and initial treatment of Wegener’s granulomatosis in childhood. Arthritis Rheum., 2009, 60(11), p. 3413–3424.

19. CALVO-RÍO, V., LORICERA, J., MATA, C. et al. Henoch-schönlein purpura in Northern Spain: Clinical spectrum of the disease in 417 patients from a single center, Medicine (United States), 2014, 93(2), p. 106–113.

20. CARLSON, J. A., NG, B. T., CHEN, K. R. Cutaneous vasculitis update: Diagnostic criteria, classifica-tion, epidemiology, etiology, pathogenesis, evaluation and prognosis, Am. J. Dermatopathol., 2005, 27(6), p. 504–528.

21. CARUSO, C., GENCARELLI, G., GAETA, F. et al. Efficacy of omalizumab treatment in a man with occupational asthma and eosinophilic granulomatosis with polyangioitis. Ann. Allergy, Asthma Immunol., 2018, 120(2), p. 209–211.

22. COHEN, P., PAGNOUX, C., MAHR, A. et al. Churg-Strauss syndrome with poor-prognosis factors: A prospective multicenter trial comparing glucocorticoids and six or twelve cyclophosphamide pulses in forty-eight patients. Arthritis Care Res., 2007, 57(4), p. 686–693.

23. COMARMOND, C., PAGNOUX, C., KHELLAF, M. et al. Eosinophilic granulomatosis with polyangiitis (Churg-Strauss): Clinical characteristics and long--term followup of the 383 patients enrolled in the French Vasculitis Study Group cohort. Arthritis Rheum., 2013, 65(1), p. 270–281.

24. CUNDIFF, J., KANSAL, S., KUMAR, A. et al. Cogan’s syndrome: A cause of progressive hearing deafness. Am. J. Otolaryngol. – Head Neck Med. Surg., 2006, 27(1), p. 68–70.

25. D’AGUANNO, V., RALLI, M., DE VINCENTIIS, M. et al. Optimal management of Cogan’s syndrome: A multidisciplinary approach. J. Multidisciplin. Healthcare, 2018, 11, p. 1–11.

26. DAVIS, M. D. P., DAOUD, M. S., KIRBY, B. et al. Clinicopathologic correlation of hypocomplementemic and normocomplementemic urticarial vasculitis. J. Am. Acad. Dermatol., 1998, 38(6 I), p. 899–905.

27. DAVIS, M. D. P., DAOUD, M. S., McEVOY, M. T. et al. Cutaneous manifestations of Churg-Strauss syndrome: A clinicopathologic correlation. J. Am. Acad. Dermatol., 1997, 37 (2 I), p. 199–203.

28. DAVID, C., JACHIET, M., PINETON DE CHAMBRUN, M. et al. Chronic obstructive pulmonary disease associated with hypocomplementemic urticarial vasculitis. J. Allergy Clin. Immunol. Pract., 2020, 8(9), p. 3222–3224.e1.

29. DeREMEE, R. A., SPECKS, U., DANIEL SU, W. P. Cutaneous Wegener’s granulomatosis: Clinical, histopathologic, and immunopathologic features of thirty patients. J. Am. Acad. Dermatol., 1994, 31(4), p. 605–612.

30. Di LERNIA, V., LOMBARDI, M., LO SCOCCO, G. Infantile acute hemorrhagic edema and rotavirus infection. Pediatr. Dermatol., 2004, 21(5), p. 548–550.

31. Di PIETRO, G. M., CASTELLAZZI, M. L., MASTRANGELO, A. et al. Henoch-Schönlein Purpura in children: Not only kidney but also lung. Pediatric Rheumatology, 2019, 17(1).

32. DOKTOR, V., HADI, A., HADI, A. et al. Erythema elevatum diutinum: a case report and review of literature. International Journal of Dermatology, 2019, 58(4), p. 408–415.

33. DO, N., RINGOLD, S., BRANDLING-BENNETT, H. Cutaneous polyarteritis nodosa in pediatric patients successfully treated with TNF-α inhibitor and methotrexate: Case series and literature review. Pediatr. Dermatol., 2019, 36(6), p. 932–935.

34.     DUMOUCHEL, W., SMITH, E. T., BEASLEY, R. et al. Association of asthma therapy and Churg-Strauss syndrome: An analysis of postmarketing surveillance data. Clin. Ther., 2004, 26(7), p. 1092–1104.

35.     E MOURA GARCIA, C. S., SOKOLOVA, A., TORRE, M. L. et al. Acute Hemorrhagic Edema of Infancy. Eur. Ann. Allergy Clin. Immunol., 2016, 48(1), p. 22–26.

36. ERDEN, A., BATU, E. D., SÖNMEZ, H. E. et al. Comparing polyarteritis nodosa in children and adults: a single center study. Int. J. Rheum. Dis., 2017, 20(8), p. 1016–1022.

37. ESATOGLU, S. N., KUTLUBAY, Z., HATEMI, G. Highlights of the 18th International Conference on Beh-çet’s syndrome. Clin. Exp. Rheumatol., 2018, 36(6), p. 3–12.

38. FELICETTI, M., GASPAROTTO, M., FRIGO, A. C. et al. Renal involvement at baseline can predict major renal relapse in anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis. Clin. Exp. Rheumatol., 2020, 38(2), p. 201–206.

39. FERREIRO, J. E., PASARIN, G., QUESADA, R. et al. Benign hypergammaglobulinemic purpura of Waldenström associated with Sjögren’s syndrome. Case report and review of immunologic aspects. Am. J. Med., 1986, 81(4), p. 734–740.

40. FINDER, K. A., McCOLLOUGH, M. L., DIXON, S. L. et al. Hypergammaglobulinemic purpura of Waldenström. J. Am. Acad. Dermatol., 1990, 23(4), p. 669–676.

41. FURUTA, S., IWAMOTO, T., NAKAJIMA, H., Update on eosinophilic granulomatosis with polyangiitis. Allergology International, 2019, 68(4), p. 430–436.

42. GENOVESE, G., TAVECCHIO, S., BERTI, E. et al. Pyoderma gangrenosum-like ulcerations in granulomatosis with polyangiitis: two cases and literature review, Rheumatol. Internat., 2018, 38(6), p. 1139–1151.

43. GILCHRIST, H., PATTERSON, J. W. Erythema nodosum and erythema induratum (nodular vasculitis): Diagnosis and management. Dermatologic Therapy, 2010, 23(4), p. 320–327.

44. GINSBERG, S., ROSNER, I., SLOBODIN, G. et al. Infliximab for the treatment of refractory polyarteritis nodosa. Clin Rheumatol, 2019, 38(10), p. 2825–2833.

45. GIOFFREDI, A., MARITATI, F., OLIVA, E. et al. Eosinophilic granulomatosis with polyangiitis: An overview. Frontiers in Immunology, 2014, 5, (NOV).

46. GIUGGIOLI, D., MANFREDI, A., LUMETTI, F. et al. Cryoglobulinemic vasculitis and skin ulcers. Our therapeutic strategy and review of the literature. Seminars in Arthritis and Rheumatism, 2015, 44(5), p. 518–526.

47. GOLSHEVSKY, D., CHEUNG, M., BURGNER, D. Kawasaki disease: The importance of prompt recognition and early referral. Aust. Fam. Physician, 2013, 42(7), p. 473–476.

48. GRAU, R. G. Churg-Strauss syndrome: 2005–2008 update. Current Rheumatology Reports, 2008, 10(6), p. 453–458.

49. GRECO, A., DE VIRGILIO, A., RIZZO, M. I. et al. Microscopic polyangiitis: Advances in diagnostic and therapeutic approaches. Autoimmunity Reviews, 2015, 14(9), p. 837–844.

50. GRECO, A., GALLO, A., FUSCONI, M. et al. Cogan’s syndrome: An autoimmune inner ear disease. Autoimmunity Reviews, 2013, 12(3), p. 396–400.

51. GRECO, A., MARINELLI, C., FUSCONI, M. et al. Clinic manifestations in granulomatosis with polyangiitis. Intern. J. Immunopathol. Pharmacol., 2016, 29(2), p. 151–159.

52. GROH, M., MASCIOCCO, G., KIRCHNER, E. et al. Heart transplantation in patients with eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome). J. Hear. Lung Transplant., 2014, 33(8), p. 842–850.

53. HA, T. S., LEE, J. S. Scrotal involvement in childhood Henoch-Schönlein purpura. Acta Paediatr. Int. J. Paediatr., 2007, 96(4), p. 552–555.

54. HAMAD, A., JITHPRATUCK, W., KRISHNASWAMY, G. Urticarial vasculitis and associated disorders. Ann. Allergy, Asthma Immunol., 2017, 118(4), p. 394–398.

55. HAMADA, H., SUZUKI, H., ONOUCHI, Y. et al. Efficacy of primary treatment with immunoglobulin plus ciclosporin for prevention of coronary artery abnormalities in patients with Kawasaki disease predicted to be at increased risk of non-response to intravenous immunoglobulin (KAICA): a randomised controlled, open-label, blinded-endpoints, phase 3 trial. Lancet, 2019, 393(10176), p. 1128–1137.

56. HERNÁNDEZ-RODRÍGUEZ, J., CARBONELL, C., MIRÓN-CANELO, J. A. et al. Rituximab treatment for IgA vasculitis: A systematic review. Autoim. Rev, 2020, 19, (4).

57. HOFFMAN, G. S., KERR, G. S., LEAVITT, R. Y. et al. Wegener granulomatosis: An analysis of 158 patients. Ann Intern Med, 1992, 116(6), p. 488–498.

58. HOLLE, J. U., DUBRAU, C., HERLYN, K. et al. Rituximab for refractory granulomatosis with polyangiitis (Wegener’s granulomatosis): Comparison of efficacy in granulomatous versus vasculitic manifestations. Ann. Rheum. Dis., 2012, 71(3), p. 327–333.

59. HUNDER, G. G., AREND, W. P., BLOCH, D. A. et al. The American College of Rheumatology 1990 criteria for the classification of vasculitis: Introduc-tion. Arthritis Rheum., 1990, 33(8), p. 1065–1067.

60. CHARTAPISAK, W., OPASTIRAKUL, S., HODSON, E. M. et al. Interventions for preventing and treating kidney disease in Henoch-Schönlein Purpura (HSP). Cochrane Database of Systematic Reviews, 2009, (3).

61. CHASSET, F., FRANCÈS, C. Cutaneous Manifesta-tions of Medium- and Large-Vessel Vasculitis. Clinical Reviews in Allergy and Immunology, 2017, 53(3), p. 452–468.

62. CHEN, K. R., TOYOHARA, A., SUZUKI, A. et al. Clinical and histopathological spectrum of cutaneous vasculitis in rheumatoid arthritis. Br. J. Dermatol., 2002, 147(5), p. 905–913.

63. CHERQAOUI, B., CHAUSSET, A., STEPHAN, J. L. et al. Intravenous immunoglobulins for severe gastrointestinal involvement in pediatric Henoch-Schönlein purpura: A French retrospective study. Arch. Pediatr., 2016, 23(6), p. 584–590.

64. CHO, K. H., LEE, D. Y., KIM, C. W. Erythema induratum of bazin. Int. J. Dermatol., 1996, 35(11), p. 802–808.

65. CHOU, T., LOUISSANT, V. R., ADAMS, A. et al. Suc-cessful treatment of henoch-schönlein purpura with recurrent gastrointestinal involvement with mycophenolate Mofetil: A brief report. Clin. Pediatr. (Phila)., 2015, 54(9), p. 900–903.

66. CHUNG, S. A., SEO, P. Microscopic Polyangiitis. Rheum Dis Clin North Am, 2010, 36(3), p. 545–558.

67. INTERNATIONAL STUDY GROUP FOR BEHÇET’S DISEASE Criteria for diagnosis of Behcet’s disease. Lancet, 1990, 335(8697), p. 1078–1080.

68. ITO, Y., ARITA, M., KUMAGAI, S. et al. Diffuse alveo-lar hemorrhage in iga vasculitis with an atypical presentation. Intern. Med., 2018, 57(1), p. 81–84.

69. JACHIET, M., FLAGEUL, B., DEROUX, A. et al. The clinical spectrum and therapeutic management of hypocomplementemic urticarial vasculitis: Data from a french nationwide study of fifty-seven patients. Arthritis Rheumatol., 2015, 67(2), p. 527–534.

70. JAYNE, D. Challenges in the management of microscopic polyangiitis: Past, present and future. Curr Opin Rheumatol, 2008, 20(1), p. 3–9.

71. JENNETTE, J. C., FALK, R. J. New insight into the pathogenesis of vasculitis associated with antineutrophil cytoplasmic autoantibodies. Curr Opin Rheumatol, 2008, 20(1), p. 55–60.

72. JENNETTE, J. C., FALK, R. J., BACON, P. A. et al. 2012 Revised International Chapel Hill consensus conference nomenclature of vasculitides. Arthritis and Rheumatism, 2013, 65 (1), p. 1–11.

73. JIAO, T., WANG, M., ZHU, X. A case of erythema elevatum diutinum associated with peripheral ulcerative keratitis. Australas. J. Dermatol., 2012, 53(1), p. 78–80.

74. JOHN, K. J., SADIQ, M., THOMAS, M. et al. Henoch-Schonlein purpura associated with HLA-B27 positive axial spondyloarthritis in a young man. BMJ Case Rep., 2019, 12(5).

75. KALLAS, R., GOLDMAN, D., PETRI, M. A. Cutaneous vasculitis in SLE. Lupus Sci. Med., 2020, 7(1), p. e000411.

76. KARADAG, O., JAYNE, D. J. Polyarteritis nodosa revisited: A review of historical approaches, subphenotypes and a research agenda. Clin Exp Rheumatol, 2018, 36, p. S135–S142.

77. KARRAS, A. Microscopic Polyangiitis: New Insights into Pathogenesis, Clinical Features and Therapy. Semin. Respir. Crit. Care Med., 2018, 39(4), p. 459–464.

78. KAWAKAMI, T., KAWANABE, T., SAITO, C. et al. Clinical and histopathologic features of 8 patients with microscopic polyangiitis including two with a slowly progressive clinical course. J. Am. Acad. Dermatol., 2007, 57(5), p. 840–848.

79. KAWAKAMI, T., SOMA, Y. Correlation of livedo racemosa, cutaneous inflammatory plaques, and antiphospholipid antibodies in patients with cutaneous polyarteritis nodosa. Medicine (Baltimore), 2011, 90(2), p. 119–124.

80. KIEFFER, C., CRIBIER, B., LIPSKER, D. Neutrophilic urticarial dermatosis a variant of neutrophilic urticaria strongly associated with systemic disease. report of 9 new cases and review of the literature. Medicine (Baltimore), 2009, 88(1), p. 23–31.

81. KIM, J. Y., CHOI, H., KIM, M. K. et al., Clinical significance of ANCA positivity in patients with IgA vasculitis: a retrospective monocentric study. Rheumatol. Int., 2019, 39 (11), p. 1927–1936.

82. KLUGER, N., PAGNOUX, C., GUILLEVIN, L. et al. Comparison of cutaneous manifestations in systemic polyarteritis nodosa and microscopic polyangiitis. Br. J. Dermatol., 2008, 159(3), p. 615–620.

83. KOLKHIR, P., GRAKHOVA, M., BONNEKOH, H. et al. Treatment of urticarial vasculitis: A systematic review. J. Allergy Clin. Immunol., 2019, 143(2), p. 458–466.

84. KOSSARD, S. Defining lymphocytic vasculitis. Australasian Journal of Dermatology, 2000, 41(3), p. 149–155.

85. KRUSCHE, M., RUFFER, N., SCHNEIDER, U. et al. Tocilizumab treatment for polyarteritis nodosa. Rheumatology (United Kingdom), 2020, 59(10), p. E63–E65.

86. KUO, H. C., LIANG, C. DI, WANG, C. L. et al. Serum albumin level predicts initial intravenous immunoglobulin treatment failure in Kawasaki disease. Acta Paediatr. Int. J. Paediatr., 2010, 99(10), p. 1578–1583.

87. KWAN, Y. W., LEUNG, C. W. Pustulo-vesicular skin eruption in a child with probable Kawasaki disease. Eur. J. Pediatr., 2005, 164(12), p. 770–771.

88. LEUNG, A. K. C., BARANKIN, B., LEONG, K. F. Henoch-Schönlein Purpura in Children: An Updated Review. Curr. Pediatr. Rev., 2020, 16(4), p. 265–276.

89. LEUNG, A. K. C., LEONG, K. F., LAM, J. M. Acute Hemorrhagic Edema of Infancy: A Diagnostic Challenge for the General Pediatrician. Curr. Pediatr. Rev., 2020, 16(4), p. 285–293.

90. LIMTONG, P., CHANPRAPAPH, K., VACHIRAMON, V. et al. Cutaneous and extracutaneous manifesta-tions of behçet’s disease linked to its disease activi-ty and prognosis. Clin. Cosmet. Investig. Dermatol., 2020, 13, p. 639–647.

91. LINSKEY, K. R., KROSHINSKY, D., MIHM, M. C. et al. Immunoglobulin-A – Associated small-vessel vasculitis: A 10-year experience at the Massachusetts General Hospital. J. Am. Acad. Dermatol., 2012, 66(5), p. 813–822.

92. LIPSKER, D. Monoclonal gammopathy of cutaneous significance: review of a relevant concept. Journal of the European Academy of Dermatology and Venereology, 2017, 31(1), p. 45–52.

93. LYNCH, J. P., DERHOVANESSIAN, A., TAZELAAR, H. et al. Granulomatosis with Polyangiitis (Wegener’s Granulomatosis): Evolving Concepts in Treatment. Seminars in Respiratory and Critical Care Medicine, 2018, 39(4), p. 434–458.

94. MAKINO, N., NAKAMURA, Y., YASHIRO, M. et al. Descriptive epidemiology of Kawasaki disease in Japan, 2011–2012: From the results of the 22nd nationwide survey. J. Epidemiol., 2015, 25(3), p. 239–245.

 95.        MARITATI, F., IANNUZZELLA, F., PAVIA, M. P. et al. Kidney involvement in medium- and large-vessel vasculitis. Journal of Nephrology, 2016, 29(4), p. 495–505.

 96. MARZANO, A. V., RAIMONDO, M. G., BERTI, E. et al. Cutaneous Manifestations of ANCA-Associated Small Vessels Vasculitis. Clinical Reviews in Allergy and Immunology, 2017, 53(3), p. 428–438.

 97.        MAZZARO, C., MAURO, E., ERMACORA, A. et al. Hepatitis C virus- related cryoglobulinemic vasculitis. Minerva Med., 2020, 112(2).

 98. MILOSLAVSKY, E. M., SPECKS, U., MERKEL, P. A. et al. Clinical outcomes of remission induction therapy for severe antineutrophil cytoplasmic antibody-associated vasculitis. Arthritis Rheum., 2013, 65(9), p. 2441–2449.

 99.        MOMEN, S. E., JORIZZO, J., AL-NIAIMI, F. Erythema elevatum diutinum: A review of presentation and treatment. Journal of the European Academy of Dermatology and Venereology, 2014, 28(12), p. 1594–1602.

100. MORGAN, A. J., SCHWARTZ, R. A. Cutaneous polyarteritis nodosa: A comprehensive review. International Journal of Dermatology, 2010, 49(7), p. 750–756.

101. MOTA, A., SAHEBGHADAM LOTFI, A., JAMSHIDI, A. R. et al. Alpha 1-antitrypsin activity is markedly decreased in Wegener’s granulomatosis. Rheumatol. Int., 2014, 34(4), p. 553–558.

102. NAKAMURA, T., KANAZAWA, N., IKEDA, T. et al. Cutaneous polyarteritis nodosa: Revisiting its definition and diagnostic criteria. Archives of Dermatological Research, 2009, 48301(1), p. 117–121.

103. NAKAZAWA, D., MASUDA, S., TOMARU, U. et al. Pathogenesis and therapeutic interventions for ANCA-associated vasculitis. Nature Reviews Rheumatology, 2019, 15(2), p. 91–101.

104. NEWBURGER, J., SCHMIEDER, G. J. Erythema Elevatum Diutinum. 2021.

105. NEWBURGER, J. W., TAKAHASHI, M., BURNS, J. C. Kawasaki Disease. Journal of the American College of Cardiology, 2016, 67(14), p. 1738–1749.

106. NGUYEN, Y., GUILLEVIN, L. Eosinophilic Granulomatosis with Polyangiitis (Churg-Strauss). Semin. Respir. Crit. Care Med., 2018, 39(4), p. 471–481.

107. NIIYAMA, S., AMOH, Y., TOMITA, M. et al. Dermatological manifestations associated with microscopic polyangiitis. Rheumatol. Int., 2008, 28(6), p. 593–595.

108. NINAN, J., LESTER, S., HILL, C. Giant cell arteritis. Best Practice and Research: Clinical Rheumatology, 2016, 30(1), p. 169–188.

109. OSTOJIC, P., JEREMIC, I. R. Managing refractory cryoglobulinemic vasculitis: Challenges and solutions. Journal of Inflammation Research, 2017, p. 49–54.

110. PAGNOUX, C., SEROR, R., HENEGAR, C. et al. Clinical features and outcomes in 348 patients with polyarteritis nodosa: A systematic retrospective study of patients diagnosed between 1963 and 2005 and entered into the French Vasculitis Study Group database. Arthritis Rheum., 2010, 62(2), p. 616–626.

111. PAGNOUX, C., MAHR, A., HAMIDOU, M. A. et al. Azathioprine or Methotrexate Maintenance for ANCA-Associated Vasculitis. N. Engl. J. Med., 2008, 359(26), p. 2790–2803.

112. PATNALA, G. P., SUNANDINI, A. P., RAYAVARAPU, R. et al. Erythema elevatum diutinum in associa-tion with IgA monoclonal gammopathy: A rare case report. Indian Dermatol. Online J., 2016, 7(4), p. 300–303.

113. PIRAM, M. AND MAHR, A. Epidemiology of immunoglobulin A vasculitis (Henoch-Schönlein): Current state of knowledge. Curr Opin Rheumatol, 2013, 25(2), p. 171–178.

114. PODJASEK, J. O., WETTER, D. A., PITTELKOW, M. R. et al. Cutaneous small-vessel vasculitis associated with solid organ malignancies: The Mayo Clinic experience, 1996 to 2009. J. Am. Acad. Dermatol., 2012, 66(2).

115. POLAT, A. K., KARAALI, M. G., AKSU, A. E. K. et al. A rare cutaneous tuberculosis form, erythema induratum of bazin: 6 years’ experience. Acta Dermatovenerologica Alpina, Pannonica Adriat., 2020, 29(3), p. 123–128.

116. POTERUCHA, T. J., WETTER, D. A., GIBSON, L. E. et al. Correlates of systemic disease in adult Henoch-Schönlein purpura: A retrospective study of direct immunofluorescence and skin lesion distribution in 87 patients at Mayo Clinic. J. Am. Acad. Dermatol., 2012, 67(4), p. 612–616.

117. POTERUCHA, T. J., WETTER, D. A., GIBSON, L. E. et al. Histopathology and correlates of systemic disease in adult Henoch-Schönlein purpura: A retrospective study of microscopic and clinical findings in 68 patients at Mayo Clinic. J. Am. Acad. Dermatol., 2013, 68(3).

118. RAINE, C., CANNING, B., MARKS, J. et al. Severe gangrene in a patient with anti-RNP positive limited cutaneous systemic sclerosis/rheumatoid arthritis overlap syndrome caused by vasculopathy and vasculitis. Eur. J. Rheumatol., 2018, 5(4), p. 269–271.

119. RAJAGOPALA, S., SHOBHA, V., DEVARAJ, U. et al. Pulmonary Hemorrhage in Henoch-Schönlein Purpura: Case Report and Systematic Review of the English Literature. Semin. Arthritis Rheum., 2013, 42(4), p. 391–400.

120. REKHTMAN, S., TANNENBAUM, R., STRUNK, A. et al. Mucocutaneous disease and related clinical characteristics in hospitalized children and adolescents with COVID-19 and multisystem inflammatory syndrome in children. J. Am. Acad. Dermatol., 2021, 84(2), p. 408–414.

121. RIMAR, D., ALPERT, A., STAROSVETSKY, E. et al. Tofacitinib for polyarteritis nodosa: A tailored therapy. Annals of the Rheumatic Diseases, 2016, 75(12), p. 2214–2216.

122. RODÓ, X., CURCOLL, R., ROBINSON, M. et al. Tropospheric winds from northeastern China carry the etiologic agent of Kawasaki disease from its source to Japan. Proc. Natl. Acad. Sci. U. S. A., 2014, 111(22), p. 7952–7957.

123. RONKAINEN, J., KOSKIMIES, O., ALA-HOUHALA, M. et al. Early prednisone therapy in Henoch-Schönlein purpura: A randomized, double-blind, placebo-controlled trial. J. Pediatr., 2006, 149(2), p. 241–247.

124. RUSSO, R. A. G., KATSICAS, M. M. Takayasu arteritis. Frontiers in Pediatrics, 6. Frontiers Media S.A., 2018.

125. ROWLEY, A. H., BAKER, S. C., SHULMAN, S. T. et al. Ultrastructural, immunofluorescence, and RNA evidence support the hypothesis of a “new” virus associated with Kawasaki disease. J. Infect. Dis., 2011, 203(7), p. 1021–1030.

126. SAADOUN, D., TERRIER, B., SEMOUN, O. et al. Hepatitis C virus associated polyarteritis nodosa. Arthritis Care Res., 2011, 63(3), p. 427–435.

127. SALIM, S. A., YOUSUF, T., PATEL, A. et al. Hypocomplementemic Urticarial Vasculitis Syndrome With Crescentic Glomerulonephritis. Am. J. Med. Sci., 2018, 355(2), p. 195–200.

128. SAULSBURY, F. T. Clinical update: Henoch-Schönlein purpura. Lancet, 2007, 369 (9566), p. 976–978.

129. SEGELMARK, M., SELGA, D., The challenge of managing patients with polyarteritis nodosa. Curr Opin Rheumatol, 2007, 19(1), p. 33–38.

130. SEGURA, S., PUJOL, R. M., TRINDADE, F. et al. Vasculitis in erythema induratum of Bazin: A histopathologic study of 101 biopsy specimens from 86 patients. J. Am. Acad. Dermatol., 2008, 59(5), p. 839–851.

131. SHAVIT, E., ALAVI, A., SIBBALD, R. G. Vasculitis–What Do We Have to Know? A Review of Literature. International Journal of Lower Extremity Wounds, 2018, 17(4), p. 218–226.

132. SHIMIZU, A., TANAKA, K., TAKAZAWA, S. et al. A large superior mesenteric artery aneurysm and ileal obstruction: A rare presentation of polyarteritis nodosa in an infant. Oxford Med. Case Reports, 2019, 2019, (9), p. 401–404.

133. SHUAI, Z. W., LV, Y. F., ZHANG, M. M. et al. Clinical analysis of patients with myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis. Genet. Mol. Res., 2015, 14(2), p. 5296–5303.

134. SHUAI, Z. Q., ZHANG, C. X., SHUAI, Z. W. et al. Efficacy and safety of biological agents in the treatment of patients with takayasu arteritis: A systematic review and meta-analysis. European Review for Medical and Pharmacological Sciences, 2021, 25(1), p. 250–262.

135. SCHROETER, A. L., CONN, D. L., and JORDON, R. E. Immunoglobulin and complement deposition in skin of rheumatoid arthritis and systemic lupus erythematosus patients. Ann. Rheum. Dis., 1976, 35(4), p. 321–326.

136. SCHNEIDER, J. W., JORDAAN, H. F. The histopathologic spectrum of erythema induratum of Bazin. Am. J. Dermatopathol., 1997, 19(4), p. 323–333.

137. SILVA, F., PINTO, C., BARBOSA, A. et al. New in-sights in cryoglobulinemic vasculitis. Journal of Autoimmunity, 2019, 105. Academic Press.

138. SINGH, S., VIGNESH, P., AND BURGNER, D. The epidemiology of Kawasaki disease: A global update. Archives of Disease in Childhood, 2015, 100(11), p. 1084–1088.

139. SMYTH, L., GASKIN, G., PUSEY, C. D. Microscopic polyangiitis. Seminars in Respiratory and Critical Care Medicine, 2004, 25(5), p. 523–533.

140. SONG, G. G., LEE, Y. H. Efficacy and safety of biological agents in patients with giant cell arteritis: A meta-analysis of randomized trials. Int. J. Clin. Pharmacol. Ther., 2020, 58(9), p. 504–510.

141. SÖNMEZ, H. E., ARMAĞAN, B., AYAN, G. et al. Polyarteritis nodosa: lessons from 25 years of experience. Clin. Exp. Rheumatol., 2019, 37(2), p. 52–56.

142. STONE, J. H. Rituximab versus cyclophosphamide for ANCA-associated vasculitis. Journal fur Mineralstoffwechsel, 2010, 17(4), p. 168.

143. SUNDERKÖTTER, C. H., ZELGER, B., CHEN, K. R. et al. Nomenclature of Cutaneous Vasculitis: Der-matologic Addendum to the 2012 Revised International Chapel Hill Consensus Conference Nomenclature of Vasculitides. Arthritis Rheumatol., 2018, 70(2), p. 171–184.

144. UEHARA, R., BELAY, E. D. Epidemiology of Kawasa-ki disease in Asia, Europe, and the United States. J. Epidemiol., 2012, 22(2), p. 79–85.

145. ULUCA, Ü., ECE, A., ŞEN, V. et al. Management of intestinal bleeding with single-dose cyclophosphamide in Henoch-Schönlein purpura. Pediatr. Int., 2015, 57(3), p. 498–500.

146. VAN WIJNGAARDEN, R. A. F. D. L., VAN RIJN, L., HAGEN, E. C. et al. Hypotheses on the etiology of antineutrophil cytoplasmic autoantibody-associated vasculitis: The cause is hidden, but the result is known. Clin J Am Soc Nephrol, 2008, 3(1), p. 237–252.

147. VANKALAKUNTI, M., JOSHI, K., JAIN, S. et al. Polyarteritis nodosa in hairy cell leukaemia: An autopsy report [2]. J Clin Pathol, 2007, 60(10), p. 1181–1182.

148. VIGUIER, M., GUILLEVIN, L., LAROCHE, L. Treat-ment of Parvovirus B19-Associated Polyarteritis Nodosa with Intravenous Immune Globulin. N. Engl. J. Med., 2001, 344(19), p. 1481–1482.

149. VOLEJNIKOVA, J., HORACEK, J., KOPRIVA, F. Dapsone treatment is efficient against persistent cutaneous and gastrointestinal symptoms in children with Henoch-Schönlein purpura. Biomed. Pap., 2018, 162(2), p. 154–158.

150. WATTS, R., LANE, S., HANSLIK, T. et al. Development and validation of a consensus methodology for the classification of the ANCA-associated vasculitides and polyarteritis nodosa for epidemiological studies. Ann. Rheum. Dis., 2007, 66(2), p. 222–227.

151. WEISS, P. F., KLINK, A. J., LOCALIO, R. et al. Corticosteroids may improve clinical outcomes during hospitalization for henoch-schönlein purpura. Pediatrics, 2010, 126(4), p. 674–681.

152. WEYAND, C. M., GORONZY, J. J. Giant-Cell Arteritis and Polymyalgia Rheumatica. N. Engl. J. Med., 2014, 371(1), p. 50–57.

153. WINKLER, A., TRUE, D. Giant Cell Arteritis: 2018 Review. Mo. Med., 2018, 115(5), p. 468–470.

154. WOLF, D., BEN-YEHUDA, A., OKON, E. et al. Nodular vasculitis associated with propylthiouracil therapy. Cutis, 1992, 49(4), p. 253–255.

155. WRIGHT, A. C., GIBSON, L. E., DAVIS, D. M. R. Cutaneous manifestations of pediatric granulomatosis with polyangiitis: A clinicopathologic and immunopathologic analysis. J. Am. Acad. Dermatol., 2015, 72(5), p. 859–867.

156. XU, H., LI, Y. M., MA, H. et al. Mycobacterium tuberculosis found at both skin lesions and Mantoux testing site in a patient with erythema induratum of Bazin. J. Dermatol., 2017, 44(10), p. 1145–1147.

157. XU, J., XU, J., LI, H. et al. Dermatomyositis combined with IgA vasculitis: A case report. Beijing Da Xue Xue Bao., 2019, 51(6), p. 1173–1177.