{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,22]],"date-time":"2025-12-22T10:35:04Z","timestamp":1766399704297,"version":"3.48.0"},"reference-count":24,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2025,12,5]],"date-time":"2025-12-05T00:00:00Z","timestamp":1764892800000},"content-version":"vor","delay-in-days":4,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Clinical Case Reports"],"published-print":{"date-parts":[[2025,12]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>Beh\u00e7et's disease is a chronic, relapsing multisystem vasculitis known for its highly variable clinical spectrum. We report the case of an 18\u2010year\u2010old male who presented with progressive headache and facial swelling. Imaging revealed extensive thrombosis involving the dural venous sinuses, superior vena cava, and left brachiocephalic vein. Despite the absence of ocular involvement or genital ulcers, a diagnosis of Beh\u00e7et's disease was established based on recurrent oral ulcers, cutaneous findings, vascular thrombosis, and a positive pathergy test, fulfilling the International Criteria for Beh\u00e7et's Disease. The patient was treated with corticosteroids, azathioprine, colchicine, and rivaroxaban, resulting in clinical and radiologic improvement. This case highlights a rare and aggressive vascular manifestation of Beh\u00e7et's disease in an adolescent, emphasizing the need for early diagnosis and immunosuppressive management to prevent long\u2010term complications.<\/jats:p>","DOI":"10.1002\/ccr3.71616","type":"journal-article","created":{"date-parts":[[2025,12,6]],"date-time":"2025-12-06T04:12:21Z","timestamp":1764994341000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Atypical Pediatric\u2010Onset Beh\u00e7et's Disease Presenting With Superior Vena Cava Thrombosis in an Adolescent Male: A Case Report"],"prefix":"10.1002","volume":"13","author":[{"given":"Ubaid","family":"Ullah","sequence":"first","affiliation":[{"name":"Lady Reading Hospital  Peshawar Pakistan"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tahreem","family":"Mari","sequence":"additional","affiliation":[{"name":"Dow Medical College  Karachi 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