{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,12]],"date-time":"2026-03-12T10:17:24Z","timestamp":1773310644938,"version":"3.50.1"},"reference-count":15,"publisher":"SAGE Publications","license":[{"start":{"date-parts":[[2025,6,16]],"date-time":"2025-06-16T00:00:00Z","timestamp":1750032000000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"},{"start":{"date-parts":[[2025,6,16]],"date-time":"2025-06-16T00:00:00Z","timestamp":1750032000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Sage Open Medical Case Reports"],"published-print":{"date-parts":[[2025,12]]},"abstract":"<jats:p>Neurological Behcet\u2019s disease is a rare systemic vasculitis marked by recurrent oral or genital ulcers, eye manifestations of uveitis or retinal vasculitis, and skin lesions. This report details a case of neurological Behcet\u2019s disease in a 14-year-old Somali male who presented with bilateral pan uveitis, genital ulcers, altered level of consciousness, and seizure. The patient met 2014 International Criteria for Behcet Disease. Magnetic resonance imaging demonstrated abnormal hyperintensity to bilateral hippocampi and mesial temporal lobes. Spine magnetic resonance imaging revealed patchy long segment T2 signal abnormality of the central spinal cord and patchy enhancement at T6. He received IV methylprednisolone, IV infliximab, and then oral prednisone. This case demonstrates children with neurological Behcet\u2019s disease can present with hippocampus involvement and transverse myelitis. Physicians should consider neurological Behcet\u2019s disease in pediatric patients presenting with altered level of consciousness or seizure. It illustrates the importance of timely intervention in mitigating the neurological complications associated with neurological Behcet\u2019s disease.<\/jats:p>","DOI":"10.1177\/2050313x251346246","type":"journal-article","created":{"date-parts":[[2025,6,16]],"date-time":"2025-06-16T08:46:01Z","timestamp":1750063561000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":1,"title":["Neurological Behcet\u2019s disease with transverse myelitis in an adolescent: A case report"],"prefix":"10.1177","volume":"13","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-1937-1330","authenticated-orcid":false,"given":"Jeanine","family":"McColl","sequence":"first","affiliation":[{"name":"Division of Rheumatology, Department of Pediatrics, University of Calgary, AB, Canada"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Teresa","family":"Liang","sequence":"additional","affiliation":[{"name":"Department of Radiology, University of Alberta, Edmonton, AB, Canada"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dax G.","family":"Rumsey","sequence":"additional","affiliation":[{"name":"Division of Rheumatology, Department of Pediatrics, University of Alberta, Edmonton, AB, Canada"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2025,6,16]]},"reference":[{"key":"e_1_3_2_2_2","doi-asserted-by":"publisher","DOI":"10.1212\/WNL.0b013e318238edeb"},{"key":"e_1_3_2_3_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.msard.2019.101906"},{"key":"e_1_3_2_4_2","doi-asserted-by":"publisher","DOI":"10.1177\/03000605241311446"},{"key":"e_1_3_2_5_2","unstructured":"CARE Development Group. 2013 CARE Case Report guidelines (Internet) https:\/\/www.care-statement.org\/checklist (2013 accessed 28 May 2025)."},{"key":"e_1_3_2_6_2","doi-asserted-by":"publisher","DOI":"10.1007\/s10067-004-0944-1"},{"key":"e_1_3_2_7_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.msard.2015.07.003"},{"key":"e_1_3_2_8_2","doi-asserted-by":"publisher","DOI":"10.1177\/1352458511431077"},{"key":"e_1_3_2_9_2","doi-asserted-by":"publisher","DOI":"10.1111\/j.1468-1331.2007.01754.x"},{"key":"e_1_3_2_10_2","doi-asserted-by":"publisher","DOI":"10.1016\/j.jns.2011.07.053"},{"issue":"4","key":"e_1_3_2_11_2","first-page":"312","article-title":"Role of diffusion-weighted MRI in neuro-Behcet`s disease","volume":"11","author":"Alharbi FS","year":"2006","unstructured":"Alharbi FS, Albadr FB, Alorainy IA, et al. Role of diffusion-weighted MRI in neuro-Behcet`s disease. Neurosciences 2006; 11(4): 312\u2013314.","journal-title":"Neurosciences"},{"issue":"4","key":"e_1_3_2_12_2","article-title":"Clinical characteristics of paediatric neuro-Beh\u00e7et\u2019s disease: a single tertiary centre experience","volume":"32","author":"Cakar N","year":"2014","unstructured":"Cakar N, Ba\u015faran O, Uncu N, et al. Clinical characteristics of paediatric neuro-Beh\u00e7et\u2019s disease: a single tertiary centre experience. Clin Exp Rheumatol 2014; 32(4 suppl 84): S165\u2013S170.","journal-title":"Clin Exp Rheumatol"},{"issue":"8","key":"e_1_3_2_13_2","first-page":"1588","article-title":"Neuro-Beh\u00e7et is a rare disease but should be considered in all kinds of neurological findings, even in childhood","volume":"40","author":"T\u00fct\u00fcnc\u00fc Toker R","year":"2022","unstructured":"T\u00fct\u00fcnc\u00fc Toker R, Bodur M, Bican Demir A, et al. Neuro-Beh\u00e7et is a rare disease but should be considered in all kinds of neurological findings, even in childhood. 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