Amyloidosis secondary to xanthogranulomatous pyelonephritis: A rare association

Xanthogranulomatous pyelonephritis and secondary systemic amyloidosis are re-latively common pathologies with innumerable cases being reported now and then. However the association of these entities is an extremely uncommon occurrence with only ten cases described in the literature. Clinical remissi...

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Main Authors: Punia Rajpal, Dhingra Neerja, Mohan Harsh, D′Cruz Sanjay
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2010-01-01
Series:Saudi Journal of Kidney Diseases and Transplantation
Online Access:http://www.sjkdt.org/article.asp?issn=1319-2442;year=2010;volume=21;issue=4;spage=720;epage=723;aulast=Punia
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author Punia Rajpal
Dhingra Neerja
Mohan Harsh
D′Cruz Sanjay
author_facet Punia Rajpal
Dhingra Neerja
Mohan Harsh
D′Cruz Sanjay
author_sort Punia Rajpal
collection DOAJ
description Xanthogranulomatous pyelonephritis and secondary systemic amyloidosis are re-latively common pathologies with innumerable cases being reported now and then. However the association of these entities is an extremely uncommon occurrence with only ten cases described in the literature. Clinical remission of amyloidosis develops in a majority of these patients after re-moval of the renal lesion. We present a case of this rare association in a young female who under-went nephrectomy for a non-functioning kidney. A histopathological diagnosis of xanthogranu-lomatous pyelonephritis was made. In addition there were deposits of amyloid in the glomeruli and the interstitial blood vessels.
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spelling doaj.art-5cd2648eee2545ceb6ca77c8acd88e9b2022-12-21T18:48:05ZengWolters Kluwer Medknow PublicationsSaudi Journal of Kidney Diseases and Transplantation1319-24422010-01-01214720723Amyloidosis secondary to xanthogranulomatous pyelonephritis: A rare associationPunia RajpalDhingra NeerjaMohan HarshD′Cruz SanjayXanthogranulomatous pyelonephritis and secondary systemic amyloidosis are re-latively common pathologies with innumerable cases being reported now and then. However the association of these entities is an extremely uncommon occurrence with only ten cases described in the literature. Clinical remission of amyloidosis develops in a majority of these patients after re-moval of the renal lesion. We present a case of this rare association in a young female who under-went nephrectomy for a non-functioning kidney. A histopathological diagnosis of xanthogranu-lomatous pyelonephritis was made. In addition there were deposits of amyloid in the glomeruli and the interstitial blood vessels.http://www.sjkdt.org/article.asp?issn=1319-2442;year=2010;volume=21;issue=4;spage=720;epage=723;aulast=Punia
spellingShingle Punia Rajpal
Dhingra Neerja
Mohan Harsh
D′Cruz Sanjay
Amyloidosis secondary to xanthogranulomatous pyelonephritis: A rare association
Saudi Journal of Kidney Diseases and Transplantation
title Amyloidosis secondary to xanthogranulomatous pyelonephritis: A rare association
title_full Amyloidosis secondary to xanthogranulomatous pyelonephritis: A rare association
title_fullStr Amyloidosis secondary to xanthogranulomatous pyelonephritis: A rare association
title_full_unstemmed Amyloidosis secondary to xanthogranulomatous pyelonephritis: A rare association
title_short Amyloidosis secondary to xanthogranulomatous pyelonephritis: A rare association
title_sort amyloidosis secondary to xanthogranulomatous pyelonephritis a rare association
url http://www.sjkdt.org/article.asp?issn=1319-2442;year=2010;volume=21;issue=4;spage=720;epage=723;aulast=Punia
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AT mohanharsh amyloidosissecondarytoxanthogranulomatouspyelonephritisarareassociation
AT dx2032cruzsanjay amyloidosissecondarytoxanthogranulomatouspyelonephritisarareassociation