Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/12305
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dc.contributor.authorHo, Prahladen
dc.contributor.authorSmith, Caroleen
dc.date.accessioned2015-05-16T01:58:08Z
dc.date.available2015-05-16T01:58:08Z
dc.date.issued2014-06-16en
dc.identifier.citationCase Reports in Hematology 2014; 2014(): 269359en
dc.identifier.govdoc25031876en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/12305en
dc.description.abstractErdheim-Chester disease (ECD) is a rare multisystem non-Langerhans histiocytosis. CNS involvement is a major complication, which is often rapidly progressive and confers a poor prognosis. However, treatment of CNS ECD is difficult due to poor CNS penetrance by the most effective chemotherapeutic drugs commonly used in this disorder (e.g., interferon and cladribine). We describe a case of a 60-year-old lady with a 5-year history of stable systemic ECD who presented with new brainstem lesions and rapid, steroid-refractory neurological deterioration which required immediate intervention. High-dose methotrexate was chosen due to its rapid onset of action and excellent CNS penetration. Her neurological deterioration was quickly arrested with significant functional improvement, which was sustained for 4 months with consolidation doses of high-dose methotrexate. Subsequent treatment with cladribine and interferon did not confer any appreciable clinical improvement. High-dose methotrexate is effective in controlling rapidly progressive CNS ECD and should be considered as a salvage agent prior to commencement of more definitive treatment.en
dc.language.isoenen
dc.titleHigh-dose methotrexate for the treatment of relapsed central nervous system erdheim-chester disease.en
dc.typeJournal Articleen
dc.identifier.journaltitleCase reports in hematologyen
dc.identifier.affiliationDepartment of Clinical Haematology, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.doi10.1155/2014/269359en
dc.description.pages269359en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/25031876en
dc.type.austinJournal Articleen
item.languageiso639-1en-
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item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
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