Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/55394
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dc.contributor.authorSelva-Nayagam, D.-
dc.contributor.authorPhipps, S.-
dc.contributor.authorO'Connell, J.-
dc.contributor.authorWhite, V.-
dc.contributor.authorRootman, J.-
dc.date.issued2003-
dc.identifier.citationClinical and Experimental Ophthalmology, 2003; 31(1):78-82-
dc.identifier.issn1442-6404-
dc.identifier.issn1442-9071-
dc.identifier.urihttp://hdl.handle.net/2440/55394-
dc.descriptionJournal compilation © 2008 Royal Australian and New Zealand College of Ophthalmologists-
dc.description.abstractTwo cases are presented of orbital cholesterol granuloma associated with gradual proptosis arising in men aged 35 and 41 years. Computed tomography demonstrated osteo-lytic masses in the frontal bone at the lacrimal fossa. Curettage revealed a characteristic histology of foreign body reactions surrounding cholesterol clefts. In both cases abnormal bone, more consistent with fibrous dysplasia than reactive change, was found at the periphery. The finding of abnormal bone associated with orbital cholesterol granulomas suggests that a pre-existing bone anomaly may be present in a subset of these cases.-
dc.description.statementofresponsibilityDinesh Selva, Simon E. Phipps, John X. O’Connell, Valerie A. White and Jack Rootman-
dc.language.isoen-
dc.publisherBlackwell Publishing Asia-
dc.subjectcholesterol granuloma-
dc.subjectfibrous dysplasia-
dc.subjectfrontal bone-
dc.subjectorbit-
dc.subjectosteolytic lesion.-
dc.titlePathogenesis of orbital cholesterol granuloma-
dc.typeJournal article-
dc.identifier.doi10.1046/j.1442-9071.2003.00605.x-
pubs.publication-statusPublished-
dc.identifier.orcidSelva-Nayagam, D. [0000-0002-2169-5417]-
Appears in Collections:Aurora harvest
Surgery publications

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