Universidad Peruana Cayetano Heredia

HaNDL syndrome and seizures: An unusual presentation

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dc.contributor.author Bedoya-Sommerkamp, Marcelo
dc.contributor.author Medina-Ranilla, Jesús
dc.contributor.author Chau-Rodríguez, Victor
dc.contributor.author Málaga-Espinoza, Bárbara
dc.contributor.author Escalaya, Alejandro L.
dc.contributor.author Burneo, Jorge G.
dc.date.accessioned 2022-12-14T14:25:33Z
dc.date.available 2022-12-14T14:25:33Z
dc.date.issued 2022
dc.identifier.uri https://hdl.handle.net/20.500.12866/12875
dc.description.abstract The Headache and Neurologic Deficits with cerebrospinal fluid Lymphocytosis syndrome (HaNDL) is a rare, benign and self-limited entity of unknown cause, diagnosed by exclusion. It usually presents with neurological deficits such as hemiparesthesia, dysphasia and hemiparesis. However, seizures are not usually associated with the clinical spectrum of this syndrome. Here we report a case of a 35 year-old male patient with multiple episodes of moderate-severe headaches with transient hemiparesthesia, dysarthria, confusion, visual hallucinations, disinhibited behavior, and a bilateral tonic-clonic seizure. HaNDL diagnosis was made after clinical improvement and CSF evolution. Clinicians should consider HaNDL syndrome in patients presenting with headache, seizures, and confusion, when all other etiologies are ruled out. en_US
dc.language.iso eng
dc.publisher Elsevier
dc.relation.ispartofseries Clinical Neurology and Neurosurgery
dc.rights info:eu-repo/semantics/restrictedAccess
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es
dc.subject HaNDL syndrome en_US
dc.subject seizures en_US
dc.title HaNDL syndrome and seizures: An unusual presentation en_US
dc.type info:eu-repo/semantics/article
dc.identifier.doi https://doi.org/10.1016/j.clineuro.2022.107515
dc.subject.ocde https://purl.org/pe-repo/ocde/ford#3.02.25
dc.subject.ocde https://purl.org/pe-repo/ocde/ford#3.02.11
dc.relation.issn 1872-6968


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