Publication:
Nervous system dysfunction in Henoch-Schonlein syndrome: systematic review of the literature

cris.virtualsource.author-orcidfee31f3a-7949-4c63-9897-4b69b65cac3c
cris.virtualsource.author-orcid2ed23f44-5eeb-430f-bfa7-4729016790a8
datacite.rightsopen.access
dc.contributor.authorGarzoni, Luca
dc.contributor.authorVanoni, Federica
dc.contributor.authorRizzi, Mattia
dc.contributor.authorSimonetti, Giacomo
dc.contributor.authorGoeggel Simonetti, Barbara
dc.contributor.authorRamelli, Gian P
dc.contributor.authorBianchetti, Mario Giovanni
dc.date.accessioned2024-10-14T07:47:14Z
dc.date.available2024-10-14T07:47:14Z
dc.date.issued2009
dc.description.abstractOBJECTIVE: CNS or peripheral nervous system dysfunction sometimes occurs in Henoch-Schönlein patients. METHODS: We review all Henoch-Schönlein cases published after 1969 with CNS dysfunction without severe hypertension and neuroimaging studies (n = 35), cranial or peripheral neuropathy (n = 15), both CNS and peripheral nervous system dysfunction without severe hypertension (n = 2) or nervous system dysfunction with severe hypertension (n = 2). Forty-four of the 54 patients were <20 years of age. RESULTS: In patients with CNS dysfunction without or with severe hypertension the following presentations were observed in decreasing order of frequency: altered level of consciousness, convulsions, focal neurological deficits, visual abnormalities and verbal disability. Imaging studies disclosed the following lesions: vascular lesions almost always involving two or more vessels, intracerebral haemorrhage, posterior subcortical oedema, diffuse brain oedema and thrombosis of the superior sagittal sinus. Following lesions were noted in the subjects with cranial or peripheral neuropathy without severe hypertension: peroneal neuropathy, peripheral facial palsy, Guillain-Barré syndrome, brachial plexopathy, posterior tibial nerve neuropathy, femoral neuropathy, ulnar neuropathy and mononeuritis multiplex. Persisting signs of either CNS (n = 9) or peripheral (n = 1) nervous system dysfunction were sometimes reported. CONCLUSIONS: In Henoch-Schönlein syndrome, signs of nervous system dysfunction are uncommon but clinically relevant. This review helps clinicians managing Henoch-Schönlein syndrome with nervous system dysfunction.
dc.description.numberOfPages6
dc.description.sponsorshipUniversitätsklinik für Kinderheilkunde
dc.identifier.doi10.7892/boris.31831
dc.identifier.isi000272081000014
dc.identifier.pmid19797041
dc.identifier.publisherDOI10.1093/rheumatology/kep282
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/105271
dc.language.isoen
dc.publisherOxford University Press
dc.publisher.placeOxford
dc.relation.ispartofRheumatology
dc.relation.issn1462-0324
dc.relation.organizationDCD5A442BADAE17DE0405C82790C4DE2
dc.titleNervous system dysfunction in Henoch-Schonlein syndrome: systematic review of the literature
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage9
oaire.citation.issue12
oaire.citation.startPage1524
oaire.citation.volume48
oairecerif.author.affiliationUniversitätsklinik für Kinderheilkunde
oairecerif.author.affiliationUniversitätsklinik für Kinderheilkunde
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unibe.date.licenseChanged2019-10-28 00:52:30
unibe.description.ispublishedpub
unibe.eprints.legacyId31831
unibe.journal.abbrevTitleRHEUMATOLOGY
unibe.subtype.articlecontribution

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