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Article: Optic neuritis as the initial clinical presentation of limbic encephalitis: a case report

TitleOptic neuritis as the initial clinical presentation of limbic encephalitis: a case report
Authors
KeywordsOptic neuritis
Limbic encephalitis
Autoimmune encephalitis
Paraneoplastic syndrome
Issue Date2018
PublisherBioMed Central Ltd. The Journal's web site is located at http://www.jmedicalcasereports.com/
Citation
Journal of Medical Case Reports, 2018, v. 12 n. 1, article no. 357, p. 1-5 How to Cite?
AbstractBackground: Limbic encephalitis is characterized by rapid onset of working memory deficit, mood changes, and often seizures. The condition has a strong paraneoplastic association, but not all cases are invariably due to tumors. Case presentation: We present a case of limbic encephalitis in a Chinese patient who initially presented to our hospital with optic neuritis and no other neurological symptoms. The diagnosis was made radiologically, and cognitive and neurological symptoms did not occur until 5 months later. Extensive investigations for autoimmune, infective, and neoplastic causes were all negative. A working diagnosis of paraneoplastic neurological syndrome was made, and the patient is being managed with high-dose steroid therapy according to the Optic Neuritis Treatment Trial protocol during relapses, as well as with tumor surveillance. Conclusions: This case highlights ocular symptoms as important clues for diagnosing neurological diseases, as well as autoimmune encephalitis as an important differential diagnosis in the management of “idiopathic” optic neuritis in the Chinese population.
Persistent Identifierhttp://hdl.handle.net/10722/265954
ISSN
2020 SCImago Journal Rankings: 0.287
PubMed Central ID

 

DC FieldValueLanguage
dc.contributor.authorCheung, SSL-
dc.contributor.authorLau, GKK-
dc.contributor.authorChan, KH-
dc.contributor.authorWong, YHI-
dc.contributor.authorLai, JSM-
dc.contributor.authorTang, WK-
dc.contributor.authorShih, KC-
dc.date.accessioned2018-12-17T02:16:21Z-
dc.date.available2018-12-17T02:16:21Z-
dc.date.issued2018-
dc.identifier.citationJournal of Medical Case Reports, 2018, v. 12 n. 1, article no. 357, p. 1-5-
dc.identifier.issn1752-1947-
dc.identifier.urihttp://hdl.handle.net/10722/265954-
dc.description.abstractBackground: Limbic encephalitis is characterized by rapid onset of working memory deficit, mood changes, and often seizures. The condition has a strong paraneoplastic association, but not all cases are invariably due to tumors. Case presentation: We present a case of limbic encephalitis in a Chinese patient who initially presented to our hospital with optic neuritis and no other neurological symptoms. The diagnosis was made radiologically, and cognitive and neurological symptoms did not occur until 5 months later. Extensive investigations for autoimmune, infective, and neoplastic causes were all negative. A working diagnosis of paraneoplastic neurological syndrome was made, and the patient is being managed with high-dose steroid therapy according to the Optic Neuritis Treatment Trial protocol during relapses, as well as with tumor surveillance. Conclusions: This case highlights ocular symptoms as important clues for diagnosing neurological diseases, as well as autoimmune encephalitis as an important differential diagnosis in the management of “idiopathic” optic neuritis in the Chinese population.-
dc.languageeng-
dc.publisherBioMed Central Ltd. The Journal's web site is located at http://www.jmedicalcasereports.com/-
dc.relation.ispartofJournal of Medical Case Reports-
dc.rightsJournal of Medical Case Reports. Copyright © BioMed Central Ltd.-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectOptic neuritis-
dc.subjectLimbic encephalitis-
dc.subjectAutoimmune encephalitis-
dc.subjectParaneoplastic syndrome-
dc.titleOptic neuritis as the initial clinical presentation of limbic encephalitis: a case report-
dc.typeArticle-
dc.identifier.emailLau, GKK: gkklau@hku.hk-
dc.identifier.emailChan, KH: koonho@hku.hk-
dc.identifier.emailWong, YHI: wongyhi@hku.hk-
dc.identifier.emailLai, JSM: laism@hku.hk-
dc.identifier.emailShih, KC: kcshih@hku.hk-
dc.identifier.authorityLau, GKK=rp01499-
dc.identifier.authorityChan, KH=rp00537-
dc.identifier.authorityWong, YHI=rp01467-
dc.identifier.authorityLai, JSM=rp00295-
dc.identifier.authorityShih, KC=rp01374-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/s13256-018-1893-7-
dc.identifier.pmid30509326-
dc.identifier.pmcidPMC6276199-
dc.identifier.scopuseid_2-s2.0-85057596090-
dc.identifier.hkuros296380-
dc.identifier.volume12-
dc.identifier.issue1-
dc.identifier.spagearticle no. 357, p. 1-
dc.identifier.epagearticle no. 357, p. 5-
dc.publisher.placeUnited States-
dc.identifier.issnl1752-1947-

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