Abstract
Behçet’s disease is distinguished by a triad of chronic oral aphthae, recurrent genital ulcers and uveitis, generally referred to as ‘the triple syndrome’. Behçet’s disease is also thought to be a multisystemic disease consisting of varying combinations of ocular, mucocutaneous, neurologic, cardiovascular, pulmonary, renal, gastrointestinal, and other manifestations.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Behçet H (1940) Some observations on the clinical picture of the so-called triple Symptom complex. Dermatologica 81: 73–83
Jensen T (1941) Sur les ulcerations aphteuses de la muqueues de la bouche et de la peau genitale combiness avec les sumptomes oculaires (Syndrome Behçet). Acta Derm Venereol 22: 64–79
Sezer PN (1953) The Isolation of a virus as the cause of Behçet’s disease. Am J Ophthalmol 36: 301–15
Bouzas A (1956) The Adamantiadis-Behçet’s Syndrome. Bull Soc Hellen Ophthalmol 24: 41
Strachau RW, Wigzell FW (1963) Polyarthritis in Behçet’s multiple Symptom complex. Ann Rheum Dis 22: 26–35
Robinson HMJ, McCrumb FRJ (1950) Comparative analysis of the mueocutaneous ocular Syndromes: report of eleven cases and review of the literature. Arch Dermatol Syphil 61: 539
Firestein GS, Gruber HE, Weisman MH, Zvaifler NJ, Barber J, O’Duffy JD (1985) Mouth and genital ulcers with inflamed cartilage: MAGIC Syndrome. Five patients with features of relapsing polychondritis and Behçet’s disease. Am J Med 79: 65–72
Levine JA, O’Duffy JD (1993) Pseudo-Behçet’s Syndrome — a description of twenty-three cases. In: Godeau P, Wechsler B (eds) Behçet’s Disease. Proceedings of the Sixth International Conference on Behçet’s Disease, Paris, 30 June to 1 July 1993.: Elsevier Science Publishers, Amsterdam, pp 295–298
Feigenbaum A (1956) Description of Behçet’s Syndrome in the Hippocratic third book of endemic disease. Br J Ophthalmol 40:355–357
Neumann I (1895) Die Aphthen am weiblichen Genitale. Wien Klin Rundsch 9: 289–90
Blüthe L (1908) Zur Kenntnis des rezidivierenden Hypopyons. Inaugural Thesis. Heidelberg
Planner H, Remenowsky F (1940) Beiträge zur Kenntnis der Ulcerationen am äusseren weiblichen Genitale. Arch Dermat Syphil 140: 162–188
Gilbert W (1925) Über chronische Verlaufsform der metastatischen Ophthalmie („Ophthalmia lenta“). Arch Augenheilkd 96: 119–130
Adamantiades B (1931) Sur un cas d’iritis a hypopyon recidivant. Ann d’Oculist 168: 271–278
Whitwell GPB (1934) Recurrent buccal and vulval ulcers with associated embolic phenomenon in skin and eye. Br J Dermatol 46: 414–419
Bebtet H (1937) Über rezidivierende aphthöse durch ein Virus verursachte Geschwüre am Mund, am Auge und an den Genitalien. Dermatol Wochenschr 105: 1152–1157
Mavioglu H (1958) Behçet’s recurrent disease. An analytical review of the literature. Mod Med 55: 1209–1222
Polychronakos DJ, Sarakotsis GP (1969) Das Adamantiades-Behçet’s Syndrome. Kun Monatsbl Augenheilkd 154: 336–341
Saylan T, Urgancioglu M, Akarcay K, Bozan G (1977) General data of the patients with Behçet’s disease. In: Dillen N, Konice M, Övül C (eds) Behc et’s Disease. Proceedings of the Second International Symposium on Behçet’s Disease, Istanbul, 29–30 September 1977. Elsevier Science Publishers, Amsterdam, pp 130–132
Aoki K, Fujioka K, Katsumata H, et al (1971) Epidemiological studies on Behçet’s disease in the Hokkaido district. Jpn J Clin Ophthalmol 25: 2239–2248
Saylan T (1993) Dermatological manifestations of Behçet’s disease in the Middle East Asia. In: Burgdorf WHC, Katz SI (eds) Dermatology — progress and perspectives. The Proceedings of the 18th World Congress of Dermatology, New York, 12–18 June 1992. The Parthenon PubUshing Group, New York, p 1074
Teter MS, Hochberg MC (1988) Diagnostic criteria and epidemiology. In: Plotkin GR, Calabro JJ, O’Duffy JD (eds) Behçet’s disease: a contemporary Synopsis. Futura Pubhshing Co., New York, pp 9–27
Chamberlain MA (1977) Behçet’s Syndrome in 32 patients in Yorkshire. Ann Rheum Dis 36: 491–499
Azizlerli G, Ozarmagan G, Övül C, Erdurak V, Saylan T, Orge C (1989) Documentation of our Behçet’s patients. In: Saylan T, Övül C, Azizlerli G, Ozarmagan B (eds) Proceedings of the Annual Meeting, Istanbul, 1989. University of Istanbul Publication, Istanbul, pp 21–6
Cho MY, Lee SH, Bang D, Lee S (1988) Epidemiologie findings of Behçet’s Syndrome. Korean J Dermatol 26: 320–329
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 2001 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Lee, S., Bang, D., Lee, ES., Sohn, S. (2001). Introduction. In: Behçet’s Disease. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-56455-0_2
Download citation
DOI: https://doi.org/10.1007/978-3-642-56455-0_2
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-63094-1
Online ISBN: 978-3-642-56455-0
eBook Packages: Springer Book Archive