Show simple item record

dc.contributor.authorShoja, MM
dc.contributor.authorArdalan, MR
dc.contributor.authorTubbs, RS
dc.contributor.authorKiuru-Enari, S
dc.date.accessioned2018-08-26T08:15:16Z
dc.date.available2018-08-26T08:15:16Z
dc.date.issued2009
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/51015
dc.description.abstractAmyloid nephropathy is an unusual manifestation of hereditary gelsolin amyloidosis and may present with proteinuria and progressive renal failure. We report the first case of renal transplantation in a patient with hereditary gelsolin amyloidosis complicated by end-stage renal disease. The patient was a 44-year-old man from the Northwest of Iran who had undergone hemodialysis for 1 year. He finally received a living, unrelated renal transplant. During a 6-year posttansplant period, the patient maintained stable allograft function without proteinuria. No significant infectious or cardiac complications were noted. Although a definite conclusion cannot be reached with a single case, this report may indicate that renal transplantation can be successfully attempted in patients with hereditary gelsolin amyloidosis and amyloid nephropathy. Renal transplantation has been performed in various hereditary, primary, and secondary amyloidoses. A brief review of this topic is presented.
dc.language.isoEnglish
dc.relation.ispartofAMERICAN JOURNAL OF THE MEDICAL SCIENCES
dc.subjectHereditary gelsolin amyloidosis
dc.subjectKidney
dc.subjectNephropathy
dc.subjectTransplant
dc.titleOutcome of Renal Transplant in Hereditary Gelsolin Amyloidosis
dc.typeArticle
dc.citation.volume337
dc.citation.issue5
dc.citation.spage370
dc.citation.epage372
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1097/MAJ.0b013e3181a4199c


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record