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Chapter 14 - Behçet Disease

from Section 2 - Inflammatory Conditions

Published online by Cambridge University Press:  15 June 2018

Louis Caplan
Affiliation:
Beth Israel-Deaconess Medical Center, Boston
José Biller
Affiliation:
Loyola University Stritch School of Medicine, Chicago
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Print publication year: 2018

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References

Akman-Demir, G., Baykan-Kurt, B., Serdaroglu, P., et al. 1996. Seven-year followup of neurologic involvement in Behçet’s syndrome. Arch Neurol, 53, 691–4.Google Scholar
Akman-Demir, G., Bahar, S., Çoban, O., et al. 1998. Cranial MRI findings in Behçet’s disease: A study of 134 MRI of 98 cases. J Neurol, 245, 362.Google Scholar
Allen, N. B. 1993. Miscellaneous vasculitic syndromes including Behçet’s disease and central nervous system vasculitis. Curr Opin Rheumatol, 5, 51–6.CrossRefGoogle ScholarPubMed
Ameri, A. and Bousser, M. G. 1992. Cerebral venous thrombosis. Neurol Clin, 10, 87111.CrossRefGoogle ScholarPubMed
Arias, M. J., Calero, E., Gil, J. F., and Paz, J. 1987. Spinal subarachnoid hematoma in Behçet’s disease. Neurosurgery, 20, 62–3.Google Scholar
Arida, A. and Sfikakis, P.P. 2014. Anti-cytokine biologic treatment beyond anti-TNF in Behçet’s disease. Clin Exp Rheumatol, 32 (Suppl. 84), S14955.Google Scholar
Assaad-Khalil, S., Abou-Seif, M., Abou-Seif, S., El-Sewy, F., and El-Sewy, M. 1993. Neurologic involvement in Behçet’s disease: Clinical, genetic and computed tomographic study. In Wechsler, B. and Godeau, P., eds., Behçet’s Disease. Amsterdam: Excerpta Medica International Congress Series, 1037, pp.409–14.Google Scholar
Bahar, S., Çoban, O., Gürvit, I. H., Akman-Demir, G., and Gökyiğit, A. 1993. Spontaneous dissection of the extracranial vertebral artery with spinal subarachnoid haemorrhage in a patient with Behçet’s disease. Neuroradiology, 35, 352–4.Google Scholar
Banna, M. and El Ramahi, K. 1991. Neurologic involvement in Behçet’s disease: Imaging findings in 16 patients. Am J Neuroradiol, 12, 791–6.Google Scholar
Bartlett, S. T., McCarthy, W. J. III, Palmer, A. S., et al. 1988. Multiple aneurysms in Behçet’s disease. Arch Surg, 123, 1004–8.CrossRefGoogle ScholarPubMed
Behçet, H. 1937. Ueber rezidivierende Aphtöse durch ein Virus verursachte Geschwüre am Mund am Auge und an den Genitalen. Dermatol Wochensch 36, 1152–7.Google Scholar
Ben-Itzhak, J., Keren, S., and Simon, J. 1985. Intracranial venous thrombosis in Behçet’s syndrome. Neuroradiology, 27, 450–1.Google Scholar
Benamour, S., Zeroual, B., Bennis, R., Amraoui, A., and Bettal, S. 1990. Maladie de Behçet: 316 cas. Presse Med, 19, 1485–9.Google Scholar
Bienenstock, H. and Murray, E. M. 1961. Behçet’s syndrome: Report of a case with extensive neurologic manifestations. N Engl J Med, 264, 1342–5.CrossRefGoogle Scholar
Bousser, M. G., Bletry, O., Launay, M., et al. 1980. Thromboses veineuses céérébrales au cours de la maladie de Behçet. Revue Neurologique, 136, 753–62.Google Scholar
Bousser, M. G., Chiars, J., and Bories, J. 1985. Cerebral venous thrombosis: A review of 38 cases. Stroke, 16, 199211.Google Scholar
Buge, A., Vincent, D., Rancurel, G., et al. 1987. Maladie de Behçet avec anévrysmes artériels multiples intracraniens. Revue Neurologique, 143, 832–5.Google Scholar
Cavara, V., and D’Ermo, F. 1954. A case of Behçet’s syndrome. XVII Concilium. Acta Ophthalmol (Copenh), 3, 1489–505.Google Scholar
Çoban, O., Bahar, S., Akman-Demir, G., et al. 1999. Masked assessment of MRI findings: Is it possible to differentiate neuro-Behçet’s disease from other central nervous system diseases? Neuroradiology, 41, 255–60.Google Scholar
Davitchi, F., Shavran, F., Akbarin, M., et al. 1997. Behçet’s disease: Analysis of 3443 cases. APLAR J Rheumatol, 1, 25.Google Scholar
Dilsen, N. 2000. About diagnostic criteria for Behçet’s disease: Our new proposal. In Bang, D., Lee, E. S., Lee, S., eds., Behçet’s Disease. Seoul: Design Mecca Publishing Co., pp. 101–4.Google Scholar
Ehrlich, G. E. 1997. Vasculitis in Behçet’s disease. Int Rev Immunol, 14, 81–8.CrossRefGoogle ScholarPubMed
Emmi, L., Salvati, G., Brugnolo, F., and Morchione, T. 1995. Immunopathological aspects of Behçet’s disease. Clin Exp Rheumatol, 13, 687–91.Google Scholar
Emmungil, H., Yaşar Bilge, N.Ş., Küçükşahin, O., et al. 2014. A rare but serious manifestation of Behçet’s disease: Intracardiac thrombus in 22 patients. Clin Exp Rheumatol, 32 (Suppl. 84), 8792.Google ScholarPubMed
Fusegawa, H., Ichikawa, Y., Tanaka, Y., et al. 1991. Blood coagulation and fibrinolysis in patients with Behçet’s disease. Rinsho Byori, 39, 509–16.Google Scholar
Gerber, S., Biondi, A., Dormont, D., Wechsler, B., and Marsault, C. 1996. Longterm MR follow-up of cerebral lesions in neuro-Behçet’s disease. Neuroradiology, 38, 761–8.Google Scholar
Godeau, P., Wechsler, B., Maaouni, A., Fagard, M., and Herreman, G. 1980. Manifestations cardiovasculaires de la maladie de Behçet. Ann Dermatol et Vénéréol, 167, 741–7.Google Scholar
Hadfield, M. G., Aydin, F., Lippman, H. R., and Sanders, K. M. 1997. Neuro-Behçet’s disease [Review]. Clin Neuropathol, 16, 5560.Google ScholarPubMed
Hampton, K. K., Chamberlain, M. A., Menon, D. K., and Davies, J. A. 1991. Coagulation and fibrinolytic activity in Behçet’s disease. Thromb Haemost, 66, 292–4.Google ScholarPubMed
Harper, M. C., O’Neill, B. P., O’Duffy, J. D., and Forbes, G. S. 1985. Intracranial hypertension in Behçet’s disease: Demonstration of sinus occlusion with use of digital subtraction angiography. Mayo Clin Proc, 60, 419–22.Google Scholar
Hassen Khoda, R., Declemy, S., Batt, M., et al. 1991. Maladie de Behçet avec atteinte artérielle multiple et volumineux angiome intra-cérébrale. Journal des Maladies Vasculaires, 16, 383–6.Google Scholar
Hatemi, G., Seyahi, E., Fresko, I., Talarico, R., and Hamuryudan, V. 2014. Behçet’s syndrome: A critical digest of the 2013–2014 literature. Clin Exp Rheumatol, 32 (Suppl. 84): S11222.Google ScholarPubMed
Herskovitz, S., Lipton, R. B., and Lantos, G. 1988. Neuro-Behçet’s disease. CT and clinical correlates. Neurology, 38, 1714–20.Google Scholar
Huong du, L. T., Wechsler, B., Piette, J. C., et al., 1993. Long term prognosis of arterial lesions in Behçet’s disease. In Wechsler, B. and Godeau, P., eds., Behçet’s Disease. Amsterdam: Excerpta Medica, pp. 557–62.Google Scholar
Imaizumi, M., Nukada, T., Toneda, S., and Abe, H. 1980. Behçet’s disease with sinus thrombosis and arteriovenous malformation in brain. J Neurol, 222, 215–8.Google Scholar
International Study Group for Behçet’s Disease. 1990. Criteria for Behçet’s disease. Lancet, 335, 1078–80.Google Scholar
Iragui, V. J. and Maravi, E. 1986. Behçet’s syndrome presenting as cerebrovascular disease. J Neurol Neurosurg Psychiatr, 49, 838–40.CrossRefGoogle ScholarPubMed
Kawakita, H., Nishimura, N., Satoh, Y., and Shibata, N. 1967. Neurological aspects of Behçet’s disease. J Neurol Sci, 5, 417–39.Google Scholar
Kidd, D., Steuer, A., Denman, M., and Rudge, P. 1999. Neurological complications in Behçet’s syndrome. Brain, 122, 2183–94.CrossRefGoogle ScholarPubMed
Kikuchi, H., Takayama, M., and Hirohata, S. 2014. Quantitative analysis of brainstem atrophy on magnetic resonance imaging in chronic progressive neuro-Behçet’s disease. J Neurol Sci, 337, 80–5.Google Scholar
Knapp, P. 1941. Beitrag zur Symptomatologie und Therapie der rezidivierenden Hypopyoniritis und der begleitenden aphtözen Schleimhauterkrankungen. Schweiz Med Wochenschr, 71, 1288–90.Google Scholar
Krespi, Y., Akman-Demir, G., Poyraz, M., et al. 2001. Cerebral vasculitis and ischaemic stroke in Behçet’s disease: Report of one case and review of the literature. Eur J Neurol, 8, 719–22.Google Scholar
Kumral, E., Evyapan, D., Oksel, F., Keser, G., and Bereketoglu, M. A. 1999. Transcranial Doppler detection of MES in patients with Behçet’s disease. J Neurol, 246, 592–5.Google Scholar
Kumral, E., Evyapan, D., Tunçel, R. 2012. Reversible cerebral venulitis in a patient with neuro-Behçet’s disease. Eur J Neurol, 19:e756.Google Scholar
Lakhanpal, S., Tani, K., Lie, J. T., et al. 1985. Pathologic features of Behçet’s syndrome: A review of Japanese autopsy registry data. Hum Pathol, 16, 790–5.CrossRefGoogle ScholarPubMed
Lehner, T. 1997. The role of heat shock protein, microbial and autoimmune agents with the aetiology of Behçet’s disease. Int Rev Immunol, 14, 2132.CrossRefGoogle ScholarPubMed
Lehner, T., Lavery, R., Smith, R., et al. 1991. Association between the 65-kilodalton heat shock protein, Streptococcus sanguis, and the corresponding antibodies in Behçet’s syndrome. Infect Immun, 59, 1434–41.Google Scholar
Macchi, P., Grossman, R. I., Gomori, J. M., et al. 1986. High field MR imaging of cerebral venous thrombosis. J Comput Assist Tomogr, 10, 10–5.CrossRefGoogle Scholar
Masheter, H. C. 1959. Behçet’s syndrome complicated by intracranial thrombophlebitis. Proc R Soc Med, 52, 1039–40.Google Scholar
Matsumoto, T., Uekusa, T., and Fukuda, Y. 1991. Vasculo-Behçet’s disease: A pathologic study of eight cases. Hum Pathol, 22, 4551.Google Scholar
Medejel, A., El Alaoui Faris, M., Al-Zemmouri, K., et al. 1986. Les manifestations neurologiques de la maladie de Behçet. Semaine des Hôpitaux, 62, 1325–8.Google Scholar
Miller, D. H., Ormerod, I. E., Gibson, A., et al. 1987. MR brain scanning in patients with vasculitis: Differentiation from multiple sclerosis. Neuroradiology, 29, 226–31.Google Scholar
Mizuki, N., Meguro, A., Ota, M., et al. 2010. Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet’s disease susceptibility loci. Nat Genet, 42: 703.CrossRefGoogle ScholarPubMed
Montalban, J., Codina, A., Alijotas, J., Ordi, J., and Khamashta, M. 1990. Magnetic resonance imaging in Behçet’s disease. J Neurol Neurosurg Psychiatry, 53, 442.Google Scholar
Morissey, S. P., Miller, D. H., Hermaszewski, R., et al. 1993. Magnetic resonance imaging of the central nervous system in Behçet’s disease. Eur Neurol, 33, 287–93.Google Scholar
Nagata, K. 1985. Recurrent intracranial haemorrhage in Behçet’s disease. J Neurol Neurosurg Psychiatr, 48, 190–1.Google Scholar
Nishimura, M., Satoh, K., Suga, M., and Oda, M. 1991. Cerebral angio- and neuro-Behçet’s syndrome: Neuroradiological and pathological study of one case. J Neurol Sci, 106, 1924.CrossRefGoogle ScholarPubMed
O’Duffy, J. D. 1990. Behçet’s syndrome. N Engl J Med, 322, 326–7.Google ScholarPubMed
O’Duffy, J. D. 1994. Behçet’s disease [Review]. Curr Opin Rheumatol, 6, 3943.Google Scholar
O’Duffy, J. D. and Goldstein, N. P. 1976. Neurological involvement in seven patients with Behçet’s disease. Am J Med, 61, 170–8.Google Scholar
O’Duffy, J. D., Carney, J. A., and Deodhar, S. 1971. Behçet’s disease. Report of 10 cases, 3 with new manifestations. Ann Intern Med, 75, 561–9.Google Scholar
Ozyazgan, S., Uzun, H., Onal, B., Tuzcu, A., Ugurlu, S., Andican, G. 2013. Lectin-like oxidised LDL receptor-1 as a marker of endothelial dysfunction in Behçet’s disease. Clin Exp Rheumatol, 31 (Suppl. 77), 71–6.Google Scholar
Pamir, M. N., Kansu, T., Erbengi, A., and Zileli, T. 1981. Papilledema in Behçet’s syndrome. Arch Neurol, 38, 643–5.CrossRefGoogle ScholarPubMed
Patel, D. V., Neuman, M. J., and Hier, D. B. 1989. Reversibility of CT and MR findings in neuro-Behçet’s disease. J Comput Assist Tomogr, 13, 669–73.Google Scholar
Pineton de Chambrun, M., Wechsler, B., Geri, G., Cacoub, P., and Saaddoun, D. 2012. New insights into the pathogenesis of Behçet’s disease. Autoimmun Rev, 11, 687–98.Google Scholar
Rougemont, D., Bousser, M. G., Wechsler, B., et al. 1982. Manifestations neurologiques de la maladie de Behçet. Revue Neurologique, 138, 493505.Google Scholar
Rubinstein, L. J. and Urich, H. 1963. Meningo-encephalitis of Behçet’s disease: Case report with pathological findings. Brain, 86, 151–60.CrossRefGoogle ScholarPubMed
Sakane, T. 1997. New perspective on Behçet’s disease [Review]. Int Rev Immunol, 14, 8996.Google Scholar
Saruhan-Direskeneli, G., Akman-Demir, G., Tasçi, B., Serdaroglu, P., and Eraksoy, M. 1996. Local synthesis of oligoclonal IgG is infrequent in Behçet’s disease. Rev Rheumatol, 63 Suppl, 552.Google Scholar
Serdaroglu, P. 1998. Behçet’s disease and the nervous system. J Neurol, 245, 197205.Google Scholar
Serdaroglu, P., Yazici, H., Özdemir, Ç., et al. 1989. Neurologic involvement in Behçet’s syndrome. A prospective study. Arch Neurol, 46, 265–9.Google Scholar
Shakir, R. A., Sulaiman, K., Kahn, R. A., and Rudwan, M. 1990. Neurological presentation of neuro-Behçet’s syndrome: Clinical categories. Eur Neurol, 30, 249–53.Google Scholar
Farrell, Shapiro L. S., Borhani, J. Hag-Highi, A. 2012. Tocilizumab treatment for neuro-Behçet’s disease, the first report. Clin Neurol Neurosurg, 114: 297–8.Google Scholar
Shimizu, T. 1962. Epidemiological and clinico-pathological studies on neuro-Behçet’s syndrome. Adv Neurol Sci (Tokyo), 16, 167–78.Google Scholar
Shimizu, T., Ehrlich, G. E., Inaba, G., and Hayashi, K. 1979. Behçet’s disease. Semin Arthritis Rheum, 8, 223–60.CrossRefGoogle Scholar
Stanford, M. R., Kasp, E., Whiston, R., et al. 1994. Heat shock protein peptides reactive in Behçet’s disease are uveitogenic in Lewis rats. Clin Exp Immunol, 97, 226–31.Google Scholar
Suga, M., Sato, K., Nishimura, M., and Oda, M. 1990. An autopsy case of neuro-Behçet’s disease with the middle cerebral artery occlusion on cerebral angiogram. Rinsho Shinkeigaku, 30, 1005–9.Google Scholar
Sugihara, H., Muto, Y., and Tsuchiyama, H. 1969. Neuro-Behçet’s syndrome: Report of two autopsy cases. Acta Pathology (Japan), 19, 95101.Google Scholar
Suzuki, Y., Hoshi, K., Matsuda, T., and Mizushima, Y. 1992. Increased peripheral blood T cells and natural killer cells in Behçet’s disease. J Rheumatol, 19, 588–92.Google Scholar
Tasçi, B., Direskeneli, H., Serdaroglu, P., et al. 1998. Humoral immune response to mycobacterial heat shock protein (HSP) 65 in the cerebrospinal fluid of neuro-Behçet patients. Clin Exp Immunol, 113, 100–4.Google Scholar
Taşolar, S., Doğan, M., Taşolar, H., et al. 2014. Evaluation of vertebral artery involvement by Doppler sonography in patients with Behçet disease. J Ultrasound Med, 33: 811–6.Google Scholar
Totsuka, S. and Midorikawa, T. 1972. Some clinical and pathological problems in neuro-Behçet’s syndrome. Folia Psychiatrica et Neurologica (Japan), 28, 275–84.Google Scholar
Totsuka, S., Hattori, T., and Yazari, M. 1979. Clinico-pathology of neuro-Behçet’s syndrome. In Kehner, T. and Barnes, C.G., eds., Behçet’s Disease. Clinical and Immunological Features. London: Academic Press, pp. 133–96.Google Scholar
Tsutsui, K., Hasegawa, M., Takata, M., and Takehara, K. 1998. Behçet’s disease. J Rheumatol, 25, 326–8.Google Scholar
Uruyama, A., Sakuragi, S., and Sakai, F. 1979. Angio-Behçet syndrome. In Lehner, T. and Barnes, C. G., eds., Behçet’s Syndrome. Clinical and Immunological Features. London: Academic Press, pp. 176–6.Google Scholar
Wechsler, B., Vidailhet, M., Piette, J. C., et al. 1992. Cerebral venous thrombosis in Behçet’s disease: Clinical study and long term follow-up of 25 cases. Neurology, 42, 614–8.CrossRefGoogle ScholarPubMed
Wechsler, B., Dell’Isola, B., Vidailhet, M., et al. 1993. Magnetic resonance imaging in 31 patients with Behçet disease and neurological involvement: Prospective study with clinical correlation. J Neurol Neurosurg Psychiatr, 56, 793–8.Google Scholar
Wilkins, M. R., Gove, R. I., Roberts, S. D., and Kendall, M. J. 1986. Behçet’s disease presenting as benign intracranial hypertension. Postgrad Med J, 62, 3641.Google Scholar
Wolf, S. M., Scrotland, D. L., and Phillips, L. L. 1965. Involvement of nervous system in Behçet’s syndrome. Arch Neurol, 12, 315–25.Google Scholar
Yazici, H. 1997. The place of Behçet’s syndrome among the autoimmune diseases. Int Rev Immunol, 14, 110.CrossRefGoogle ScholarPubMed
Yazici, H. 2002. Behçet’s syndrome: Where do we stand? Am J Med, 112, 75–6.Google Scholar
Yazici, H., Tüzün, Y., Pazarlı, H., et al. 1980. The combined use of HLA-B5 and the pathergy test as diagnostic markers of Behçet’s disease in Turkey. J Rheumatol, 7, 206–10.Google ScholarPubMed
Yazici, H., and Moutsopoulos, H. H. 1985. Behçet’s disease. In Lichenstein, L. M. and Fauci, A. S., eds., Current Therapy in Allergy, Immunology and Rheumatology. Philadelphia: Decker, pp. 194–7.Google Scholar
Yazici, H., Basaran, E. G., Hamuryudan, V., et al. 1996. The ten-year mortality in Behçet’s syndrome. Br J Rheumatol, 35, 139–41.Google Scholar
Zelenski, J. D., Caparo, J. A., Holden, D., and Calabrese, L. H. 1989. Central nervous system vasculitis in Behçet’s syndrome: Angiographic improvement after therapy with cytotoxic agents. Arthritis Rheum, 32, 217–20.Google Scholar

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