Publication:
Primary Systemic Amyloidosis: A Case Report

creativeworkseries.issnJNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X
dc.contributor.authorOli, Saurav Sen
dc.contributor.authorJha, Abhishek
dc.contributor.authorKarki, Anisha
dc.contributor.authorSapkota, Shova
dc.contributor.authorAdhikari, Laxman
dc.date.accessioned2025-08-25T06:16:31Z
dc.date.available2025-08-25T06:16:31Z
dc.date.issued2023
dc.descriptionSaurav Sen Oli Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal Abhishek Jha Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal Anisha Karki Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal Shova Sapkota Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal Laxman Adhikari Department of Nephrology, Kathmandu Medical College and Teaching Hospital, Sinamangal, Kathmandu, Nepal
dc.description.abstractAbstract Primary systemic amyloidosis is a systemic disease characterised by the deposition of misfolded proteins extracellularly in different organs without any known cause in the background, eventually leading to multiorgan dysfunction and death. The incidence of primary amyloidosis is estimated at 5.1-12.8 cases per million, with a poor prognosis. We report a case of a 69-year male with lower back pain, shortness of breath, and anasarca diagnosed as primary systemic amyloidosis by serum-free light chain assay and kidney needle biopsy. He was started on intravenous bortezomib and dexamethasone. Though he adhered to his medications, with time he developed renal insufficiency marked by azotemia following which hemodialysis was performed. Primary systemic amyloidosis is a rare clinical condition with a very poor prognosis. Further studies are needed to understand the proper pathophysiology and treatment of the disease.
dc.identifierhttps://doi.org/10.31729/jnma.8297
dc.identifier.urihttps://hdl.handle.net/20.500.14572/1997
dc.language.isoen_US
dc.publisherNepal Medical Association
dc.titlePrimary Systemic Amyloidosis: A Case Report
dc.typeOther
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage824
oaire.citation.startPage822
relation.isJournalIssueOfPublication22c9f6ca-26ae-4e5a-8542-94012a3e664c
relation.isJournalIssueOfPublication.latestForDiscovery22c9f6ca-26ae-4e5a-8542-94012a3e664c
relation.isJournalOfPublicatione6e146a0-0ece-4aba-aa0a-6ccfbd10a12a

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