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Optic Neuropathy Due to Chronic Lymphocytic Leukemia: the First Manifestation of the Disease

dc.contributor.authorMaleita, D
dc.contributor.authorSerras Pereira, R
dc.contributor.authorHipólito-Fernandes, D
dc.contributor.authorMoura-Coelho, N
dc.contributor.authorCunha, JP
dc.contributor.authorTavares Ferreira, J
dc.date.accessioned2021-06-15T10:15:09Z
dc.date.available2021-06-15T10:15:09Z
dc.date.issued2020-06
dc.description.abstractPurpose: Chronic lymphocytic leukemia (CLL) is the most common lymphoproliferative disorder in the western world. The involvement of the central nervous system (CNS) or the optic nerve in CLL, however, is rare. We report a case of a previously untreated patient with CLL whose first manifestation of the disease was a progressive visual loss caused by optic neuropathy. Observations: Clinical manifestations, optical coherence tomography (OCT), and automated visual fields pointed to the diagnosis of neuropathy. Leukemic involvement of the CNS was confirmed after cells suggestive of CLL were found by cerebrospinal fluid analysis. Optic nerve infiltration is thought to be the cause of this optic neuropathy, and the clinical course and treatment are described herein. Conclusions: When readily diagnosed, optic nerve infiltration is a rare, yet manageable complication of CLL.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationAm J Ophthalmol Case Rep. 2020 Jan 28;18:100603.pt_PT
dc.identifier.doi10.1016/j.ajoc.2020.100603pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/3726
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.subjectCHLC OFTpt_PT
dc.subjectOptic Neuropathypt_PT
dc.subjectChronic Lymphocytic Leukemiapt_PT
dc.subjectOptic Nerve Infiltrationpt_PT
dc.titleOptic Neuropathy Due to Chronic Lymphocytic Leukemia: the First Manifestation of the Diseasept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.startPage100603pt_PT
oaire.citation.titleAmerican Journal of Ophthalmology Case Reportspt_PT
oaire.citation.volume18pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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