Zusammenfassung
Der Morbus Behçet (MB) ist eine polyorganotrope Systemvaskulitis mit unvorhersehbarem, potentiell letalem Verlauf. Neben der klassischen Trias von Mundschleimhautaphthen, Genitalulzera und Augenentzündung [2] sind Hauterscheinungen die häufigsten Symptome, doch können prinzipiell alle Organsysteme beteiligt sein.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Literatur
Barnes CG (1979) Behçet’s syndrome — joint manifestations and synovial pathology. In: Lehner T, Barnes CG (eds) Behçet’s Syndrome — Clinical and Immunological Features. Academic Press, London, pp 199–212
Behçet H (1937) Über rezidivierende, aphthöse, durch ein Virus verursachte Geschwüre am Mund, am Auge und an den Genitalien. Dermatol Wschr 109: 1152–1157
BenEzra D, Nussenblatt R (1978) Ocular manifestations of Behçet’s disease. J oral Pathol 7: 431–435
Berman L, Trappier B, Jenkins T (1979) Behçet’s syndrome: a family study and the elucidation of a genetic role. Ann Rheum Dis 38: 118–121
Burkhardt A, Löning T (1981) Pathologische Anatomie oraler Aphthosen. Hautarzt 32: Suppl V, 302–308
Burton-Kee JE, Mowbray JF, Lehner T (1981) Different crossreacting circulating immune complexes in Behçet’s syndrome and recurrent oral ulcers. J Lab Clin Med 97: 559–567
Clausen J, Bierring F (1983) Involvement of post-capillary venules in Behçet’s disease — an electronmicroscopic study. Acta Dermatovener 63: 191–197
Cohen L (1978) Etiology, pathogenesis and classification of aphthous stomatitis and Behçet’s syndrome. J oral Pathol 7: 347–352
Denman AM, Fialkow PJ, Pelton BK, Salo AC, Appleford DJ (1979) Attempts to establish a viral aetiology for Behçet’s syndrome. In: Lehner T, Barnes CG (eds) Behçet’s Syndrome. Clinical and Immunological Features. Academic Press, London, pp 91–105
Djawari D (1984) Morbus Behçet. Untersuchungen zur Klinik, Differentialdiagnose und Pathophysiologie. Thieme, Stuttgart.
Djawari D, Hornstein OP, Schötz J (1981) Enhancement of granulocyte Chemotaxis in Behçet’s disease. Arch. Dermatol Res 270: 81–88
Dündar S (1986) Heritability of Behçet’s disease. Br J Dermatol 114: 748–749
Dunlop EMC (1979) Genital and other manifestations of Behçet’s disease seen in venereological practice. In: Lehner T, Barnes CG (eds) Behçet’s Syndrome. Clinical and Immunological Features. Academic Press, London, pp 159–176
Goolamali SK, Comaish JS, Hassanyeh F, Stephans A (1976) Familial Behçet’s syndrome. Br J Dermatol 95: 637–642
Gow P, Lehner T, Panayi GS (1979) Joint manifestations in Behçet’s syndrome and in recurrent oral ulcers. In: Lehner T, Barnes CG (eds) Behçet’s Syndrome. Clinical and Immunological Features. Academic Press, London, pp 223–240
Greenspan JS, Dadol N, Olson JA, Talal N (1981) Antibody-dependent cellular cytotoxicity in recurrent aphthous ulceration. Clin exp Immunol 44: 603–610
Haensch R (1981) Klinik der benignen oralen Aphthosis und des Morbus Behçet. Hautarzt 32: Suppl V, 308–314
Haim S (1981) Etiopathogenesis of mucocutaneous lesions in Behçet’s disease. Hautarzt 32: Suppl V, 317–320
Haneke E (1981) Behandlung der rezidivierenden Aphthen und des Morbus Behçet. Hautarzt 32: Suppl V, 320–324
Hooks JJ (1978) Possibility of a viral etiology in recurrent aphthous ulcers and Behçet’s syndrome. J oral Pathol 7: 353–364
Hori Y, Miyazawa S, Nishiyama S, Miyata M, Ishikawa S (1979) Experimental Behçet’s disease and ultrastructural microanalysis of pathological tissue. J Dermatol (Tokyo) 6: 31–37
Hornstein OP (1979) Orale Aphthen — örtliche und allgemein-medizinische Aspekte. Dtsch zahnärztl. Z 34: 808–817
Hughes RAC, Lehner (1979) Neurological aspects of Behçet’s syndrome. In: Lehner T, Barnes CG (eds) Behçet’s Syndrome. Clinical and Immunological Features. Academic Press, London, pp 241–258
Jorizzo JL (1986) Behçet’s disease. Arch Dermatol 122: 556–558
Jorizzo JL, Hudson RD, Schmalstieg FC, Daniels JC, Apisarnthanarax P, Henry JC, Gonzales EB, Ichikawa Y, Cavallo T (1984) Behçet’s syndrome: Immune regulation, circulating immune complexes, neutrophil migration, and colchicine therapy. J Am Acad Dermatol 10: 205–214
Kaneko F, Takahashi Y, Muramatsu Y, Miura Y (1985) Immunological studies on aphthous ulcer and erythema nodosum-like eruptions in Behçet’s disease. Br J Dermatol 113: 303–312
Kaneko F, Takahashi Y, Muramatsu R, Adachi K, Miura Y, Nakane A, Minagawa T (1985) Natural killer cell numbers and function in peripheral lymphoid cells in Behçet’s disease. Br J Dermatol 113: 313–318
Kato T, Minagawa T (1981) Enhancement of cytotoxicity of human peripheral blood lymphocytes by interferon. Microbiol Immunol 25: 837
Katzenellenbogen I, Feuermann EJ (1965) Beitrag zum M. Behçet (Die Bedeutung der spezifischen Hauthyperreaktivität und der Behçetinreaktion) Hautarzt 16: 13–18
Lehner T (1969) Pathology of recurrent oral ulceration and oral ulceration in Behçet’s syndrome: light, electron and fluorescence microscopy. J Pathol 97: 481–494
Lehner T (1969) Behçet’s syndrome and autoimmunity. Br Med J 1: 465–467
Lehner T (1977) Progress report: oral ulceration and Behçet’s syndrome. Gut 18: 491–511
Lehner T, Barnes CG (eds) (1979) Behçet’s Syndrome. Clinical and Immunological Features. Academic Press, London
Lehner T, Barnes CG (1986) Recent Advances in Behcet’s Disease. Roy Soc Med Int. Congr & Symp Series No. 103, London
Lehner T, Batchelor JR (1979) Classification and immunogenetic basis of Behçet’s syndrome. In: Lehner T, Barnes CG (eds) Behçet’s Syndrome. Clinical and Immunological Features. Academic Press, London, pp 13–32
Lichtig C, Haim S, Gilhar A, Hammel I, Ludatscher R (1981) Mast cells in Behçet’s disease: Ultrastructural and histamine content studies. Dermatologica 162: 167–174
Lim SD; Haw CR, Kim NY, Fusaro RM (1983) Abnormalities of T cell subsets in Behçet’s syndrome. Arch Dermatol 119: 307–310
Luderschmidt C, Wolff HH, Scherer R (1981) Immunhistologie der Läsionen bei oraler Aphthosis einschließlich Morbus Behçet. Hautarzt 32: Suppl V, 315–317
Maeda K, Nakae K (1977) Epidemiological study on dead cases of Behçet’s disease in Japan. In: Dil§en N, Koniça M, Övül C (eds) Behçet’s Disease. Excerpta Medica International Congress Series No 427, Amsterdam Oxford, pp 47–52
Martin DK, Nelms DC, Mackler BF, Peavy DL (1979) Lymphoproliferative responses induced by streptococcal antigens in recurrent aphthous stomatitis and Behçet’s syndrome. Clin Immunol Immunopathol 13: 146–155
Mason RM, Barnes CG (1969) Behçet’s syndrome with arthritis. Ann rheum Dis 28: 95–103
Matzumura N, Mizushima Y (1975) Leukocyte movement and colchicine treatment in Behçet’s disease. Lancet 2: 813
Müller W, Lehner T (1982) Quantitative electron microscopical analysis of leukocyte infiltration in oral ulcers of Behçet’s syndrome. Br J Dermatol 106: 535–544
Ohno S, Kato F, Matzuda H, Fuju N, Minagawa T (1982) Detection of γ-interferon in the sera of patients with Behçet’s disease. Inf Immun 36: 202
Oshima Y, Shimizu T, Yokohari R, Matsumoto T, Kano G, Kagami T, Magaya H (1963) Clinical studies on Behçet’s syndrome. Ann rheum Dis 22: 36–45
Reimer G, Steinkohl S, Djawari D, Hornstein OP (1982) Lytic effect of cytotoxic lymphocytes on oral epithelial cells in Behçet’s disease. Br J Dermatol 107: 529–536
Rogers RS, Sams WM, Shorter RG (1974) Lymphocytotoxicity in recurrent aphthous stomatitis and Behçet’s syndrome. Arch Dermatol 109: 361–363
Saito T, Honma T, Saigo K (1980) Epidermal Langerhans cells after the prick test for Behçet’s disease. Dermatologica 161: 152–156
Sakane T, Kotani H, Takada S, Tsunematsu T (1982) Functional aberration of T cell subsets in patients with Behçet’s disease. Arthritis Rheum 25: 1343
Saylan T, Özarmagan G, Azizlerli G, Övül C, Öke N (1986) Morbus Behçet in der Türkei. Z Hautkr 61: 1120–1122
Schotland DL, Wolf SM, White HH, Dubin HV (1963) Neurologic aspects of Behçet’s disease. Am J Med 34: 544–553
Shimizu T, Ehrlich GE, Inaba G, Hayashi K (1979) Behçet disease (Behçet syndrome) Semin Arthritis Rheum 8: 223–260
Siegismund G, Meier F, Götz G (1977) Die ulzeröse Enterokolitis, ein Symptom des Morbus Behçet. Hautarzt 28: Suppl II, 256–259
Sobel JD, Haim S, Obedeanu N, Meshulam T, Merzbach D (1977) Polymorphonuclear leucocyte function in Behçet’s disease. J Clin Pathol 30: 250–253
Sorensen B, Collet F, Rossi P, Gérard R (1985) Maladie de Behçet et pathologie cardiovasculaire. Ann Cardiol Angéiol 34: 495–497
Tiwari JL, Terasaki PI (1985) HLA and Disease Associations. Springer-Verlag, New York Berlin Heidelberg Tokyo
Valesini G, Picardo M, Pastore R, Pivetti P, Serafini U (1981) Circulating immune complexes in Behcet’s syndrome: purification, characterisation and cross-reactivity studies. Clin exp Immunol 44: 522–527
Victorino RMM, Ryan P, Hughes GRV, Hodgson HJF (1982) Cell-mediated immune function and immune-regulatory cells in Behçet’s syndrome. Clin exp Immunol 48: 125
Yamada M (1976) Immunological studies on Behçet’s disease. Aust J Dermatol 17: 41–45
Yazici H (1978) Behçet’s disease. Br Med J 2: 952
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1987 Springer-Verlag Berlin Heidelberg
About this paper
Cite this paper
Haneke, E. (1987). Morbus Behçet. In: Holzmann, H., Altmeyer, P., Marsch, W.C., Vogel, H.G. (eds) Dermatologie und Rheuma. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-72668-2_34
Download citation
DOI: https://doi.org/10.1007/978-3-642-72668-2_34
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-72669-9
Online ISBN: 978-3-642-72668-2
eBook Packages: Springer Book Archive