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dc.contributor.authorBalamtekin, Necati
dc.contributor.authorUslu, Nuray
dc.contributor.authorTemucin, Cagri
dc.contributor.authorDemir, Hulya
dc.contributor.authorTemizel, Inci Nur Saltik
dc.date.accessioned2019-12-10T11:24:21Z
dc.date.available2019-12-10T11:24:21Z
dc.date.issued2010
dc.identifier.issn1895-1058
dc.identifier.urihttps://doi.org/10.2478/s11536-009-0142-2
dc.identifier.urihttp://hdl.handle.net/11655/15638
dc.description.abstractCarpal tunnel syndrome and benign recurrent intrahepatic cholestasis are rare conditions in childhood. Benign intrahepatic cholestasis is characterized by repeated self-limited attacks of cholestasis that can start at any age and last from weeks to months. The patients are asymptomatic between these attacks. We report a 16 year-old male patient with benign recurrent intrahepatic cholestasis who developed carpal tunnel syndrome during a cholestatic attack. He was admitted with complaints of jaundice, pruritus and pain, tingling and muscle weakness in both hands for 15 days. Nerve conduction studies revealed findings compatible with carpal tunnel syndrome. He was started on ursodeoxycholic acid, fat soluble vitamins and cholestyramine and cholestasis regressed after four weeks of therapy. With the improvement of cholestasis, the symptoms of carpal tunnel syndrome also disappeared. In conclusion, benign recurrent intrahepatic cholestasis can be a rare cause of carpal tunnel syndrome in childhood. We also advocate treating the underlying disease as an appropriate conservative treatment before surgery.
dc.language.isoen
dc.publisherDe Gruyter Poland Sp Zoo
dc.relation.isversionof10.2478/s11536-009-0142-2
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectGeneral & Internal Medicine
dc.titleA Rare Cause of Carpal Tunnel Syndrome in Childhood: Benign Recurrent Intrahepatic Cholestasis
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalCentral European Journal Of Medicine
dc.contributor.departmentNöroloji
dc.identifier.volume5
dc.identifier.issue6
dc.identifier.startpage742
dc.identifier.endpage744
dc.description.indexWoS
dc.description.indexScopus


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