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Pseudotumor cerebri as the presentation of Lyme disease in a non-endemic area

dc.contributor.authorEzequiel, M
dc.contributor.authorTeixeira, AT
dc.contributor.authorBrito, MJ
dc.contributor.authorLuís, C
dc.date.accessioned2019-03-20T15:00:05Z
dc.date.available2019-03-20T15:00:05Z
dc.date.issued2018
dc.description.abstractIntracranial hypertension is a rare entity in prepubertal children, and its differential diagnosis includes a number of systemic diseases, drugs, vitamin deficiencies and excesses, and hereditary conditions. Infectious aetiology is rare. The case of a 9-year-old boy with intracranial hypertension secondary to acute neuroborreliosis is described. He presented with daily pulsatile frontotemporal headache, pallor, photophobia and phonophobia. His neurological examination revealed papilledema with no nuchal rigidity. The lumbar puncture showed increased pressure (50 cm H2O) and lymphocytic pleocytosis. Serum and cerebrospinal fluid (CSF) Borrelia burgdorferi antibodies were positive. This kind of infection is rare in Portugal but a trip to an endemic area was identified. A careful history, considering the exposure to rural areas together with the intracranial hypertension and inflammatory CSF, are important clues to the diagnosis, allowing the institution to select appropriate treatment.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationBMJ Case Rep. 2018 Mar 30;2018. pii: bcr-2017-222976pt_PT
dc.identifier.doi10.1136/bcr-2017-222976pt_PT
dc.identifier.issn1757-790X
dc.identifier.urihttp://hdl.handle.net/10400.10/2184
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherBMJ Pub. Grouppt_PT
dc.relation.publisherversionBMJ case reports.pt_PT
dc.subjectMeningitispt_PT
dc.subjectHeadachept_PT
dc.subjectTropical medicinept_PT
dc.titlePseudotumor cerebri as the presentation of Lyme disease in a non-endemic areapt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceLondonpt_PT
oaire.citation.titleBMJ case reports.pt_PT
rcaap.rightsclosedAccesspt_PT
rcaap.typearticlept_PT

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