Zusammenfassung
Unter dem klinischen Begriff kutane Vaskulitis wird ein weites Spektrum von Dermatosen verstanden, deren gemeinsames Merkmal histologische Entzündungszeichen an den Hautgefäßen und Veränderungen im umhegenden perivaskulären Gewebe sind.
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Literatur
Boom BW, Mommaas AM, Vermeer BJ (1992) Presence and interpretation of vascular immune deposits in human skin: the value of direct immunofluorescence. J Dermatol Sci 3: 26–34
Callen JP (1985) Colchicine is effective in controlling chronic cutaneous leukocytoclastic vasculitis. J Am Acad Dermatol 13: 193–200
Cupps TR, Fauci AS (1981) The vasculitides. Saunders, Philadelphia, 211 pp
DeVita S, Neri R, Bombardieri S (1991) Cyclophosphamide pulses in the treatment of rheumatic diseases: an update. Clin Exp Rheumatol 9: 179–193
Dinarello CA (1992) Interleukin-1 and tumor necrosis factor: effector cytokines in autoimmune diseases. Semin Immunol 4: 133–145
Duquesnoy B (1991) Henoch-Schönlein purpura. Baillieres Clin Rheumatol 5: 253–261
Fauci AS, Haynes BR, Costa J et al. (1982) Lymphomatoid granulomatosis. Prospective, clinical and therapeutic experience over 10 years. N Engl J Med 306: 68–74
Gaskin G, Savage CO, Ryan JJ (1991) Anti-neutrophil cytoplasmic antibodies and disease activity during longterm follow-up of 70 patients with systemic vasculitis. Nephrol Dial Transplant 6: 689–694
Horn T (1985) Long-standing erythematous facial plaques: Granuloma faciale. Arch Dermatol 121: 1553–1557
James WD, Odom RB, Katzenstein AL (1981) Cutaneous manifestations of lymphomatoid granulomatosis: Report of 44 cases and review of the literature. Arch Dermatol 117: 196–202
Katz SI, Gallin JI, Hertz KC et al. (1977) Erythema elevatum diutinum: Skin and systemic manifestations, immunologic studies, and successful treatment with dapsone. Medicine 56: 443–455
Longley J, Demar L, Feinstein RP et al. (1987) Clinical and histologic features of pityriasis lichenoides et varioliformis acuta in children. Arch Dermatol 123: 1335–1339
McCune WJ, Friedman AW (1992) Immunosuppressive drug therapy for rheumatic disease. Curr Opin Rheumatol 4: 314–312
Mertz LE, Conn DL (1992) Vasculitis associated with malignancy. Curr Opin Rheumatol 4: 39–46
Mollica F, Li Volti S, Garozzo R, Russo G (1992) Effectiveness of early prednisolone treatment in preventing the development of nephropathy in anaphylactoid purpura. Eur J Pediatr 151: 140–144
Planaguma M, Puig L, Alomar A et al. (1992) Pyoderma gangrenosum in association with erythema elevatum diutinum. Report of two cases. Cutis 49: 201–206
Sams WM (1980) Necrotizing vasculitis. J Am Acad Dermatol 3: 1–13
Sanchez NP, Van Hale HM, Su WPD (1985) Clinical and histopathological spectrum of necrotizing vasculitis: Report of findings in 101 cases. Arch Dermatol 121: 220–224
Wilkinson SM, English JSC, Smith NP et al. (1992) Erythema elevatum diutinum: A clinicopathological study. Clin Exp Dermatol 17: 87–93
Willemze R (1985) Lymphomatoid papulosis. Dermatol Clin 3: 735–747
Horio T, Danno K, Okamoto H et al. (1983) Potassium iodide in erythema nodosum and other erythematous dermatosis. J Am Acad Dermatol 9: 77–81
Schafer N, Kerdel FA (1991) Nodular vasculitis (erythema induratum) Treatment with auranofin. J Am Acad Dermatol 25: 426–429
Soderstrom RM, Krull EA (1978) Erythema nodosum: a review. Cutis 21: 806–810
Ubogy Z, Persellin RH (1982) Suppression of erythema nodosum by indomethacin. Acta Derm Venereol 62: 265–267
Upchurch KS, Heller K, Bress NM (1987) Low-dose methotrexate therapy for cutaneous vasculitis with rheumatoid arthritis. J Am Acad Dermatol 17: 355–359
Bisalbutra P, Kullavanijaya P (1993) Sulfasalazine in atrophie blanche. J Am Acad Dermatol 28: 275–276
Drucker CR, Duncan WC (1982) Antiplatelet therapy in atrophie blanche and livedo vasculitis. J Am Acad Dermatol 7: 359–363
Jetton RL, Lazarus GS (1983) Minidose heparin therapy for vasculitis of atrophie blanche. J Am Acad Dermatol 8: 23–26
Milestone LM, Braverman IM, Lucky P, Fleckman P (1983) Classification and therapy of atrophie blanche. Arch Dermatol 119: 963–969
Purcell SM, Hayes TJ (1986) Nifedipine treatment of idiopathic atrophie blanche. J Am Acad Dermatol 14: 851–854
Sams MW (1988) Livedo vasculitis. Therapy with pentoxifyllin. Arch Dermatol 124: 684–687
Sauer GC (1986) Pentoxifylline (Trental) therapy for the vasculitis of atrophie blanche. Arch Dermatol 122: 380–381
Turner AN, Whittaker S, Banks I (1990) Plasma exchange in refractory cutaneous vasculitis. Br J Dermatol 122: 411–415
Alegre VA, Winkelmann RK, Gastineau DA (1990) Cutaneous thrombosis, cerebrovascular thrombosis and lupus anticoagulant–the Sneddon syndrome. Int J Dermatol 29: 45–49
Asherson RA, Cervera R (1993) Antiphospholipid syndrome. J Invest Dermatol 100: 21S - 27S
Deffer TA, Berger TG, Gelinas-Sorell D (1987) Sneddon’s syndrome. J Am Acad Dermatol 16: 1084–1087
Falanga V, Fine MJ, Kapoor WN (1986) The cutaneous manifestations of cholesterol embolization. Arch Dermatol 112: 1194–1198
Gollnick H, Cerda JH, Bradac GB (1985) Livedo racemosa generalisata (Ehrmann) mit cerebrovaskulärer Beteiligung ( Herman-Sneddon ). Akt Dermatol 11: 17–21
Grattan CE, Burton JL (1991) Antiphospholipid syndrome and cutaneous vasoocclusive disorders. Semin Dermatol 10: 152–159
Lubach D, Stamm T, Schwabe C et al. (1990) Livedo racemosa generalisata–an evaluation of thirty-four cases. J Am Acad Dermatol 22: 633–639
Naldi L, Locati F, Marchesi L et al. (1993) Cutaneous manifestations associated with antiphospholipid antibodies in patients with suspected primary antiphospholipid syndrome: a case-control study. Ann Rheum Dis 52: 219–222
Rautenberg W, Hennerici M, Aulich A et al. (1988) Immunosuppressive therapy and Sneddon’s syndrome. Lancet II: 639–630
Stephens CJ (1992) Sneddon’s syndrome. Clin Exp Rheumatol 10: 489–492
Stockhammer G, Felber SR, Zelger B (1993) Sneddon’s syndrome: diagnosis by skin biopsy and MRI in 17 patients. Stroke 24: 685–690
Zelger B, Sepp N, Stockhammer G et al. (1993) Sneddon’s syndrome: a long-term follow-up of 21 patients. Arch Dermatol 129: 437–447
Diaz-Perez JL, Winkelmann RK (1980) Cutaneous periarteritis nodosa: A study of 33 cases. In Wolff K, Winkelmann RK (eds) Major problems in dermatology. Saunders, Philadelphia, 273 pp
Goslen JB, Graham W, Lazarus GS (1983) Cutaneous polyarteritis nodosa: Report of a case associated with Crohn’s disease. Arch Dermatol 119: 326–329
Guillevin L, Fain O, Lhote F et al. (1992) Lack of superiority of steroid plus plasma exchange to steroids alone in the treatment of polyarteritis nodosa and Churg-Strauss-Syndrom. Arthritis Rheum 35: 208–215
Thomas RH, Meyrick, Black MM (1983) The wide clinical spectrum of periarteritis nodosa with cutaneous involvement. Clin Exp Dermatol 8: 47–59
Abdullah AN, Keczkes K, Wyatt EH (1989) Skin necrosis in giant cell (temporal) arteritis: Report of three cases. Br J Dermatol 120: 843–846
Braun EW, Sams WM, Payne RR (1982) Giant cell arteritis: a systemic disease with rare cutaneous manifestations. J Am Acad Dermatol 6: 1081–1088
Doury P, Fabresse FX, Pattin S et al. (1984) La place de la dapsone dans le traitement de la maladie de Horton et de la pseudopolyarthrite rhizomelique. Aim Med Interne (Paris) 135: 31–35
Hall S, Barr W, Lie JT et al. (1985) Takayasu arteritis. A study of 32 North American patients. Medicine 64: 89–99
Hitch JM (1970) Dermatologie manifestations of giant-cell (temporal, cranial) arteritis. Arch Dermatol 101: 409–415
Hunder GG (1990) Giant cell (temporal) arteriitis. Rheum Dis Clin North Am 16: 399–409
Liozon F, Vidal E, Bonnetblanc JM et al. (1986) Disulon in the treatment of Horton’s disease. Experience with 20 patients. Ann Med Interne (Paris) 137: 299–306
Perniciaro CV, Winkelmann RK, Hunder GG (1987) Cutaneous manifestations of Takayasu’s arteritis: A clinicopathologic correlation. J Am Acad Dermatol 17: 998–1005
Brandwein S, Esdaile J, Daniff D et al. (1983) Wegener’s granulomatosis: clinical features and outcome in 13 patients. Ann Intern Med 143: 476–479
DeRemee RA, McDonald TJ, Weiland LH (1985) Wegener’s granulomatosis: observation and treatment with antimicrobial agents. Mayo Clin Proc 60: 27–32
DeRemee RA, McDonald TJ, Weiland LH (1987) Aspekte zur Therapie and Verlaufsbeobachtung der Wegener’schen Granulomatose. Med Welt 38: 470–473
Fauci AS, Haynes BF, Katz P, Wolff SM (1983) Wegener’s granulomatosis: prospective clinical therapeutic experience with 85 patients for 21 years. Ann Intern Med 98: 76–85
Gross WL, Hauschild S, Schmitt WH (1993) Immunodiagnostische and immunopathogenetische Bedeutung von Anti-Neutrophilen-Cytoplasma Antikörpern. Dtsch Med Wochenschr 118: 191–199
Hagen EC, Ballieux BE PB, Daha MR et al. (1992) Fundamental and clinical aspects of antineutrophil cytoplasmic antibodies ( ANCA ). Autoimmunity 11: 199–207
Hagen EC, Ballieux BEPB, van Es LA et al. (1993) Antineutrophil cytoplasmic autoantibodies: a review of the antigens involved, the assays, and the clinical and possible pathogenic consequences. Blood 81: 1996–2002
Hu CH, O’Loughlin S, Winkelmann RK (1977) Cutaneous manifestations of Wegener’s granulomatosis. Arch Dermatol 113: 175–182
Israel HL (1988) Sulfamethoxazol-trimethoprim therapy for Wegener’s granulomatosis. Arch Intern Med 148: 2293–2295
Jayne DR, Davies MJ, Fox CJ (1991) Treatment of systemic vasculitis with pooled intravenous immunoglobulin. Lancet 337: 1137–1139
Nölle B, Specks U, Lüdemann J et al. (1989) Anticytoplasmic autoantibodies: Their immunodiagnostic value in Wegener granulomatosis. Ann Intern Med 111: 28–40
Novack SN, Pearson CM (1971) Cyclophosphamide therapy in Wegener’s granulomatosis. N Engl J Med 284: 938–942
Raitt JW (1971) Wegener’s granulomatosis: Treatment with cytotoxic agents and adrenocorticoids. Ann Intern Med 74: 344–356
Specks S, Wheatley CL, McDonald TJ et al. (1989) Anticytoplasmic autoantibodies in the diagnosis and follow-up of Wegener’s granulomatosis. Mayo Clin Proc 64: 28–36
Steppat D, Gross WL (1989) Stage-adapted treatment of Wegener’s granulomatosis. First results of a prospective study. Klin Wochenschr 67: 666–671
Thomas RH, Payne CM, Black MM (1982) Wegener’s granulomatosis presenting as pyoderma gangrenosum. Clin;Exp Dermatol 7: 523–527
Weiner SR, Paulus HE (1989) Treatment of Wegener’s granulomatosis. Semin Respir Med 10: 156–161
Chumbley LC, Harrison EG, DeRemee RA (1977) Allergic granulomatosis and angiitis (Churg-StraussSyndrom). Report and analysis of 30 cases. Mayo Clin Proc 52: 477–484
Churg J, Strauss L (1951) Allergic granulomatosis, allergic angiitis, and periarteritis nodosa. Am J Pathol 27: 277–301
Crotty CP, DeRemee RA, Winkelmann RK (1981) Cutaneous clinicopathologic correlation of allergic granulomatosis. I Am Acad Dermatol 5: 571–581
Finan MD, Winkelmann RK (1983) The cutaneous necrotizing granuloma (Churg-Strauss syndrome) and systemic disease: review of 27 cases. Medicine 62: 142–158
Haas C, Geneau C, Odinot JM (1991) L’angeite allergique avec granulomatose: syndrome de Churg et Strauss. Ann Med Interne (Paris) 142: 335–342
Lanham JG, Elkon KB, Pusey CD, Hughes GR (1984) Systemic vasculitis with asthma and eosinophilia: a clinical approach to the Churg-Strauss syndrome. Medicine 63: 65–81
Specks U, DeRemee RA (1990) Granulomatous vasculitis: Wegener’s granulomatosis and Churg-Strauss syndrome.
Callen JP, Kalbfleisch S (1982) Urticarial vasculitis: A report of nine cases and review of the literature. Br J Dermatol 107: 87–93
Dubost JJ, Souteyrand P, Sauvezie B (1991) Drug-induced vasculitides. Baillieres Clin Rheumatol 5: 119–138
Ekenstam EAF, Callen JP (1984) Cutaneous leukocytoclastic vasculitis: Clinical and laboratory features of 82 patients seen in private practice. Arch Dermatol 120: 484–489
Gibson LE, Su WP (1990) Cutaneous vasculitis. Rheum Dis Clin North Am 16: 309–324
Goeken JA (1991) Antineutrophil cytoplasmic antibody — a useful serological marker for vasculitis. J Clin Immunol 11: 161–174
Jorizzo JL (1993) Classification of vasculitis. J Invest Dermatol 100: 1065–1108
Lancet editorial (1988) Factor VIII related antigen and vasculitis. Lancet I: 1203–1204
Lawley TJ, Kubota Y (1990) Vasculitis. Dermatol Clin 8: 681–687
Mackel SE (1982) Treatment of vasculitis. Med Clin North Am 66: 941–954
Mader R, Keystone EC (1992) Infections that cause vasculitis. Curr Opin Rheumatol 4: 35–38
Monroe EW (1981) Urticarial vasculitis: An updated review. J Am Acad Dermatol 5: 88–95
Pusey CD (1990) Plasma exchange in immunological disease. Prog Clin Biol Res 337: 419–424
Sanchez NP, Van Hale HM, Su WP (1985) Clinical and histopathologic spectrum of necrotizing vasculitis. Report of findings in 101 cases. Arch Dermatol 121: 220–224
Smoller BR, McNutt NS, Contreras F (1990) The natural history of vasculitis. Arch Dermatol The antiphospholipid syndrome.Br J Dermatol 125: 199–210
Tsokos M, Lazarou SA, Moutsopoulos HM (1987) Vasculitis in primary Sjögren’s syndrome: Histologic classification and clinical presentation. Am J Clin Pathol 88: 26–31
Venning MC, Quinn A, Broomhead V, Bird AG (1990) Antibodies directed against neutrophils ( C-ANCA and P-ANCA) are of distinct diagnostic value in systemic vasculitis. Q J Med 77: 1287–1296
Wolff K, Winkelmann RK (1980) Vasculitis. Saunders, Philadelphia
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Orfanos, C.E., Garbe, C. (1995). Vaskulitis. In: Therapie der Hautkrankheiten. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-97602-5_18
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DOI: https://doi.org/10.1007/978-3-642-97602-5_18
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