{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,22]],"date-time":"2025-10-22T17:43:35Z","timestamp":1761155015470,"version":"3.33.0"},"reference-count":24,"publisher":"Wiley","issue":"11","license":[{"start":{"date-parts":[[2005,12,12]],"date-time":"2005-12-12T00:00:00Z","timestamp":1134345600000},"content-version":"vor","delay-in-days":3328,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Arthritis &amp; Rheumatism"],"published-print":{"date-parts":[[1996,11]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Beh\u00e7et's disease is a multisystem inflammatory disorder which may involve the vascular system. The vasculopathy of Beh\u00e7et's disease is distinctive among the vasculitides in that it involves both arteries and veins, and vessels of all sizes. Most published diagnostic criteria for Beh\u00e7et's disease include the classic triad of orogenital ulceration and ocular inflammation. In this report, we describe a patient who had a vasculopathy fitting the Beh\u00e7et's disease type, but who lacked the other characteristic or diagnostic features of Beh\u00e7et's disease. This case illustrates an unusual presentation and natural history of a complex vasculitic disease.<\/jats:p>","DOI":"10.1002\/art.1780391122","type":"journal-article","created":{"date-parts":[[2007,2,14]],"date-time":"2007-02-14T11:48:53Z","timestamp":1171453733000},"page":"1926-1930","source":"Crossref","is-referenced-by-count":15,"title":["Beh\u00e7et\u2010type vasculopathy in a patient without the diagnostic features of Beh\u00e7et disease"],"prefix":"10.1002","volume":"39","author":[{"given":"Brian D.","family":"Golden","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Archana","family":"Goel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hal J.","family":"Mitnick","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,12,12]]},"reference":[{"key":"e_1_2_1_2_2","first-page":"1152","article-title":"Uber rezidivierende aphtose, durch ein virus verursachte Geschwure am Mund, am Auge und an den Genitalien","volume":"105","author":"Beh\u00e7et H","year":"1937","journal-title":"Dermatol Wochenschr"},{"key":"e_1_2_1_3_2","doi-asserted-by":"publisher","DOI":"10.1016\/0049-0172(79)90004-0"},{"key":"e_1_2_1_4_2","first-page":"1078","article-title":"Criteria for diagnosis of Beh\u00e7et's disease","volume":"335","author":"International Study Group for Beh\u00e7et's Disease","year":"1990","journal-title":"Lancet"},{"key":"e_1_2_1_5_2","first-page":"341","article-title":"Vascular involvement in Beh\u00e7et's disease: arterial and venous and vessels of all sizes (editorial)","volume":"19","author":"Lie JT","year":"1992","journal-title":"J Rheumatol"},{"key":"e_1_2_1_6_2","first-page":"402","article-title":"Vascular involvement in Beh\u00e7et's disease","volume":"19","author":"Ko\u00e7 Y","year":"1992","journal-title":"J Rheumatol"},{"key":"e_1_2_1_7_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0344-0338(88)80135-3"},{"key":"e_1_2_1_8_2","doi-asserted-by":"crossref","first-page":"1077","DOI":"10.1016\/S0889-857X(21)00486-5","article-title":"Vasculitis associated with connective tissue disorders","volume":"21","author":"Bacon PA","year":"1995","journal-title":"Rheum Dis Clin North Am"},{"key":"e_1_2_1_9_2","doi-asserted-by":"crossref","first-page":"423","DOI":"10.1016\/S0889-857X(21)01067-X","article-title":"Vasculitis in Beh\u00e7et's disease","volume":"16","author":"O'Duffy JD","year":"1990","journal-title":"Rheum Dis Clin North Am"},{"key":"e_1_2_1_10_2","first-page":"1186","article-title":"Pathologically defined neuro\u2010, vasculo\u2010, and entero\u2010Beh\u00e7et's disease","volume":"12","author":"Katoh K","year":"1985","journal-title":"J Rheumatol"},{"key":"e_1_2_1_11_2","doi-asserted-by":"publisher","DOI":"10.1136\/ard.52.11.823"},{"key":"e_1_2_1_12_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0889-857X(21)00056-9"},{"volume-title":"Primer on the Rheumatic Diseases","year":"1993","author":"Pyeritz RE","key":"e_1_2_1_13_2"},{"key":"e_1_2_1_14_2","doi-asserted-by":"publisher","DOI":"10.3949\/ccjm.61.6.438"},{"key":"e_1_2_1_15_2","doi-asserted-by":"crossref","first-page":"350","DOI":"10.1177\/096721099400200312","article-title":"Cerebrovascular accidents resulting from segmental mediolytic arteriopathy of the cerebral arteries in young adults","volume":"2","author":"Leu HJ","year":"1994","journal-title":"Cardiovasc Surg"},{"key":"e_1_2_1_16_2","doi-asserted-by":"publisher","DOI":"10.1177\/000331979304400608"},{"key":"e_1_2_1_17_2","doi-asserted-by":"publisher","DOI":"10.1007\/BF01959219"},{"key":"e_1_2_1_18_2","first-page":"3332","article-title":"Human leukocyte antigen serologic and DNA typing of Beh\u00e7et's disease and its primary association with B51","volume":"33","author":"Mizuki N","year":"1992","journal-title":"Invest Ophthalmol Vis Sci"},{"key":"e_1_2_1_19_2","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM199002013220509"},{"key":"e_1_2_1_20_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0190-9622(80)80363-X"},{"key":"e_1_2_1_21_2","doi-asserted-by":"publisher","DOI":"10.1016\/S0190-9622(94)70102-4"},{"key":"e_1_2_1_22_2","first-page":"199","article-title":"Beh\u00e7et's syndrome with central nervous system involvement in a Tanzanian African","volume":"46","author":"Makene WJ","year":"1969","journal-title":"East Afr Med J"},{"key":"e_1_2_1_23_2","doi-asserted-by":"publisher","DOI":"10.1007\/BF02000674"},{"key":"e_1_2_1_24_2","doi-asserted-by":"publisher","DOI":"10.1016\/0190-9622(92)70124-X"},{"key":"e_1_2_1_25_2","doi-asserted-by":"publisher","DOI":"10.1097\/00005382-199422000-00012"}],"container-title":["Arthritis &amp; 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