{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,6]],"date-time":"2026-05-06T11:20:56Z","timestamp":1778066456643,"version":"3.51.4"},"reference-count":10,"publisher":"Scientific Scholar","content-domain":{"domain":["surgicalneurologyint.com"],"crossmark-restriction":true},"short-container-title":[],"abstract":"\n Background:<\/jats:title>\n Focal cortical dysplasia (FCD) is a congenital abnormality of the cerebral cortex and a common cause of epilepsy. However, FCD in the hippocampus is rare.<\/jats:p>\n <\/jats:sec>\n \n Case Description:<\/jats:title>\n A 30-year-old woman was admitted to the hospital because of seizures. Brain magnetic resonance imaging showed focal cortical thickening of the right medial temporal lobe cortex. The patient underwent a right-sided anteromedial temporal lobectomy. Pathologic examination showed disorganized cortical gray matter tissue with large dysmorphic cortical neurons, supporting a FCD diagnosis. The histological findings of hippocampal sclerosis were not found.<\/jats:p>\n <\/jats:sec>\n \n Conclusion:<\/jats:title>\n The present case is a rare case of dysmorphic neurons without histological findings of sclerosis in the hippocampus reported. Recognizing more hippocampal FCD-related epilepsy cases is essential to better understanding the condition.<\/jats:p>\n <\/jats:sec>","DOI":"10.25259\/sni_465_2025","type":"journal-article","created":{"date-parts":[[2025,12,12]],"date-time":"2025-12-12T07:32:29Z","timestamp":1765524749000},"page":"527","update-policy":"https:\/\/doi.org\/10.25259\/crossmark_policy","source":"Crossref","is-referenced-by-count":1,"title":["Temporal epilepsy associated with hippocampal focal cortical dysplasia"],"prefix":"10.25259","volume":"16","author":[{"given":"Thi Phuoc Yen","family":"Tran","sequence":"first","affiliation":[{"name":"Department of Neurosurgery, Vinmec Central Park International Hospital, Ho Chi Minh, Vietnam"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"The Khanh","family":"Dang","sequence":"additional","affiliation":[{"name":"Department of Orthopaedics, Vinmec Times City International Hospital, Hanoi, Vietnam"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nu Tra My","family":"Ton","sequence":"additional","affiliation":[{"name":"Department of Radiology, Vinmec Central Park International Hospital, Ho Chi Minh, Vietnam"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Thi Hong Khang","family":"Bui","sequence":"additional","affiliation":[{"name":"Department of Laboratory, Division of Histopathology, Vinmec Central Park International Hospital, Ho Chi Minh, Vietnam"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Minh Chau","family":"Tran","sequence":"additional","affiliation":[{"name":"Department of Radiology, Vinmec Central Park International Hospital, Ho Chi Minh, Vietnam"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nhu Phuc","family":"Tran","sequence":"additional","affiliation":[{"name":"Department of Laboratory, Division of Histopathology, Vinmec Central Park International Hospital, Ho Chi Minh, Vietnam"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Van Tri","family":"Truong","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Vinmec Central Park International Hospital, Ho Chi Minh, Vietnam"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"10894","published-online":{"date-parts":[[2025,12,12]]},"reference":[{"key":"10.25259\/SNI_465_2025\/ref-1","doi-asserted-by":"crossref","first-page":"200","DOI":"10.1016\/j.brainres.2005.10.088","article-title":"Dysmorphic neurons in patients with temporal lobe epilepsy","volume":"1072","author":"Da Silva","year":"2006","journal-title":"Brain Res"},{"key":"10.25259\/SNI_465_2025\/ref-2","doi-asserted-by":"crossref","first-page":"2079","DOI":"10.1093\/brain\/awp145","article-title":"Multi-focal occurrence of cortical dysplasia in epilepsy 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