Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/18288
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dc.contributor.authorNesbitt, Alexander Luke-
dc.contributor.authorKhan, Munad-
dc.contributor.authorHoag, Nathan-
dc.contributor.authorLokan, Julie-
dc.date2018-
dc.date.accessioned2018-08-30T04:08:01Z-
dc.date.available2018-08-30T04:08:01Z-
dc.date.issued2018-07-18-
dc.identifier.citationBMJ Case Reports 2018; 2018: bcr-2018-225414en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/18288-
dc.description.abstractWe report the case of a 46-year-old man who initially presented with macroscopic haematuria. Although initially concerning for a malignancy in the bladder, histology demonstrated a primary bladder amyloidosis that has remained stable for 6 years since the initial diagnosis. Primary bladder amyloidosis is an important clinical entity that can mimic bladder malignancy on clinical history, radiological investigation and cystoscopic evaluation. Although uncommon, it should not be neglected as a possible diagnosis in patients presenting with haematuria.en_US
dc.language.isoeng-
dc.subjecthematuriaen_US
dc.subjecturological surgeryen_US
dc.subjecturologyen_US
dc.titlePrimary bladder amyloidosis as a cause of haematuria.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleBMJ Case Reportsen_US
dc.identifier.affiliationDepartment of Urology, Cairns Hospital, Cairns, Queensland, Australiaen_US
dc.identifier.affiliationUrologyen_US
dc.identifier.affiliationPathologyen_US
dc.identifier.doi10.1136/bcr-2018-225414en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-0741-5383en_US
dc.identifier.orcid0000-0002-4140-1500en_US
dc.identifier.pubmedid30021741-
dc.type.austinJournal Article-
local.name.researcherLokan, Julie
item.languageiso639-1en-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptGastroenterology and Hepatology-
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