Urticarial vasculitis

Bibliography:
1. Hypocomplementia with cutaneous vasculitis and arthritis: Possible immune complex syndrome / R С McDuffie, W. Mitchell Sams, J.E. Maldonado [et al.] // Mayo. Clin. Proc. 1973. №48. R. 340-348; 2. Soter N.A. Chronic urticaria as a manifestation of necrotizing venulitis//N. Engl.J. Med. 1977. №296. R. 1440-1442; 3. Huston D.P, Bressler R.B. Urticaria and angioedema // Med. Clin.N. Amer. 1992. № 76. P. 805-840; 4. Soter N.A., Austen K. R, Gigli I. Urticaria and arthralgias as manifestations of necrotizing angiitis (vasculitis) // J. Invest. Dermatol. 1974. № 63. R. 485-490; 5. Agnello V., Ruddy S., Winchester R.J., Christian C.L., Kunkel H.G. Hereditary C2 deficiency in systemic lupus erythematosus and acquired complement abnormalities in an unusual SLE-related syndrome//Birth. Defects. 1975. № 11. R. 312-317; 6. A hypocomplementemic vasculitic urticarial syndrome: Report of four new cases and definition of the disease / C.R. Zeiss, RX. Burch, R.J. Marder [et al.] //Am.J. Med. 1980. №68. R. 867-875; 7. Black A. K. Urticarial vasculitis // Clin. Dermatol. 1999. №17. R. 565-569; 8. Aboobaker J., Greaves M.W Urticarial vasculitis // Clin.Exp. Dermatol. 1986. № 11. R. 436-444; 9. Gibson L. E., Su W P. Cutaneous vasculitis // Rheum. Dis. Clin. North. Am. 1990. № 16. R. 309-324; 10. Mehregan D.R., Hall M.J., Gibson L. E. Urticarial vasculitis: a histopathologicand clinical reviewof 72 cases// J.Am. Acad. Dermatol. 1992. № 26. R. 441-448; 11. Sanchez N.P, Wnkelmann R.K., Schroeter A. L, Dick-en C.H. The clinical and histopathologic spectrums of urticarial vasculitis: study of forty cases // J.Am. Acad. Dermatol. 1982. № 7. R. 599-605; 12.Asherson R.A., D»Cruz D., Stephens С J., McKee P. H., Hughes G. R. Urticarial vasculitis in aconnective tissue disease clinic: patterns, presentations, and treatment // Semin. Arthritis. Rheum. 1991. № 20. R. 285-296; 13. Hypocomplementemicurticarial vasculitis syndrome with severe systemic manifestations /A. Martini, A. Ravelli, S. Albani [et al.] // J. Pediatr. 1994. № 124. R. 742-744; 14. Waldo F.B., Leist P. A., Strife C.R, Forristal J., West С D. Atypical hypocomplementemic vasculitis syndrome in a child//J. Pediatr. 1985. № 106. R. 745-750; 15. Cadnapaphornchai M.A., Saulsbury F.T., Norwood V. F. Hypocomplementemic urticarial vasculitis:report of a pediatric case // Pediatr. Nephrol. 2000. № 14. R. 328-331; 16. Renard M., Wouters C, Proesmans W. Rapidly progressive glomerulonephritis is a boy with hypocomplementaemic urticarial vasculitis// Eur. J. Pediatr. 1998. № 157. P. 243-245; 17. Monroe E.W. Urticarial vasculitis: an updated review // J.Am. Acad. Dermatol. 1981. №5. R. 88-95; 18. Berg R.E., KantorG.R., Bergfeld W F. Urticarial vasculitis// Int. J. Dermatol. 1988. № 27. R. 468-472; 19. Kano Y, Orihara M, Shiohara T. Cellular and molecular dynamics in exercise-induced urticarial vasculitis lesions //Arch. Dermatol. 1998. № 134. R. 62-67; 20 Systemic lupus erythematosus presenting with normo-complementemic urticarial vasculitis in a 4-year-old girl /A. Soy-lu, S. Kavukcu, N. Uzuner// Pediatr. Int. 2001. № 43. R. 420-422; 21. Davis A. E III: C1 INH and hereditary angioneurotic edema //Annu. Rev. Immunol. 1988. № 6. R. 595-627; 22. Venzor J., Lee W.L, Huston D.P. Urticarial vasculitis // Clin.Rev. Allergy.lmmunol. 2002. №23. R. 201-216; 23. Taillandier J., Alemanni M., Emile J.F. Normocomple-mentemic urticarial vasculitis inaugurating destructive polyarthritis // Joint. Bone. Spine. 2001. № 68. R. 510-512; 24. Hong L., Wackers R, Dewar M., Kashgarian M., Aske-nase P. W. Atypical fatal hypocomplementemicurticarial vasculitis with involvement of native and homograft aortic valves in an African American man // J. Allergy. Clin. Immunol. 2000. № 106. R. 1196-1198; 25. Renal transplantationin a patient with hypocomplementemic urticarial vasculitis syndrome / P. Grimbert, К Scholte, С Buisson[etal.]//Am.J. Kidney. Dis. 2001. №37. R. 144-148; 26. Recurrent cutaneous necrotizing eosinophilic vasculitis. A novel eosinophil-mediated syndrome / К Chen, M.R. Pittelkow, D. Su [etal.]//Arch. Dermatol. 1994. № 130. R. 1159-1166; 27. Messiaen T, Van Damme В., Kuypers D., Maes В., Van-renterghem Y Crescentic glomerulonephritis complicating the course of a hypocomplementemic urticarial vasculitis // Clin. Nephrol. 2000. № 54. R. 409-412; 28. Chen H.J., Bloch К J. Hypocomplementemic urticarial vasculitis, jaccoud»sarthropathy, valvular heart disease, and reversible tracheal stenosis: a surfeit of syndromes//J. Rheumatol. 2001. № 28. R. 383-386; 29. Skytta E., Pohjankoski H., Savolainen A. Etaner-cept and urticaria in patients with juvenile idiopathic arthritis // Clin.Exp. Rheumatol. 2000. № 18. R. 533-534; 30. Wsnieski J.J., Jones S. M. IgG autoantibodies to the collagen-like region of C1q in hypocomplementemic urticarial vasculitis syndrome, systemic lupus erythematosus, and 6 other musculoskeletalor rheumatic diseases // J. Rheumatol. 1992. №19. R. 884-888; 31. Agnello V, Koffler D., Eisenberg J.W., Wnchester R.J., Kundel H.G. C1q precipitins in the sera ofpatients with systemic lupus erythematosus and other hypocomplementemic states: characterization of high and low molecular weight types // J.Exp. Med. 1971. №34. R. 228-241; 32. Soma J., Sato H., Ito S., Saito T. Nephrotic syndrome associated with hypocomplementaemic urticarial vasculitis syndrome: successful treatment with cyclosporine II k. Nephrol. Dial. Trans. 1999. № 14. R. 1753-1757; 33. Thuong-Nguyen V, Kadunce D.P, Hendrix J.D., Gammon W.R., Zone J.J. Inhibition of neutrophiladherence to antibody by dapsone: a possible therapeutic mechanism of dapsone in the treatmentof IgA dermatoses // J. Invest. Dermatol. 1993. №100. R. 349-355.