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A Rare Case of Hematuria; Primary Amyloidosis of the Bladder Neck

Primary and localized amyloidosis of the urinary tract is considered to be a rare clinical entity with approximately 160 cases documented in the literature. Here we present a case of a 77 year old gentleman with painless visible hematuria. Flexible cystoscopy revealed abnormal and polypoidal bladder...

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Detalles Bibliográficos
Autores principales: Tolofari, Sotonye, Ansari, Asif, Knight, Ross J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148768/
https://www.ncbi.nlm.nih.gov/pubmed/27957427
http://dx.doi.org/10.1016/j.eucr.2016.11.005
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author Tolofari, Sotonye
Ansari, Asif
Knight, Ross J.
author_facet Tolofari, Sotonye
Ansari, Asif
Knight, Ross J.
author_sort Tolofari, Sotonye
collection PubMed
description Primary and localized amyloidosis of the urinary tract is considered to be a rare clinical entity with approximately 160 cases documented in the literature. Here we present a case of a 77 year old gentleman with painless visible hematuria. Flexible cystoscopy revealed abnormal and polypoidal bladder mucosa. Transurethral resection of these lesions revealed histology with congo-red staining and positive green-apple birefringence, these findings are consistent with amyloidosis. There has so far been no sign of recurrence in this gentleman, with routine cystoscopic surveillance. Here we present a literature review on the presentation, diagnosis and management of this rare condition.
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spelling pubmed-51487682016-12-12 A Rare Case of Hematuria; Primary Amyloidosis of the Bladder Neck Tolofari, Sotonye Ansari, Asif Knight, Ross J. Urol Case Rep Inflammation and Infection Primary and localized amyloidosis of the urinary tract is considered to be a rare clinical entity with approximately 160 cases documented in the literature. Here we present a case of a 77 year old gentleman with painless visible hematuria. Flexible cystoscopy revealed abnormal and polypoidal bladder mucosa. Transurethral resection of these lesions revealed histology with congo-red staining and positive green-apple birefringence, these findings are consistent with amyloidosis. There has so far been no sign of recurrence in this gentleman, with routine cystoscopic surveillance. Here we present a literature review on the presentation, diagnosis and management of this rare condition. Elsevier 2016-12-06 /pmc/articles/PMC5148768/ /pubmed/27957427 http://dx.doi.org/10.1016/j.eucr.2016.11.005 Text en Crown Copyright © 2016 Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Inflammation and Infection
Tolofari, Sotonye
Ansari, Asif
Knight, Ross J.
A Rare Case of Hematuria; Primary Amyloidosis of the Bladder Neck
title A Rare Case of Hematuria; Primary Amyloidosis of the Bladder Neck
title_full A Rare Case of Hematuria; Primary Amyloidosis of the Bladder Neck
title_fullStr A Rare Case of Hematuria; Primary Amyloidosis of the Bladder Neck
title_full_unstemmed A Rare Case of Hematuria; Primary Amyloidosis of the Bladder Neck
title_short A Rare Case of Hematuria; Primary Amyloidosis of the Bladder Neck
title_sort rare case of hematuria; primary amyloidosis of the bladder neck
topic Inflammation and Infection
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148768/
https://www.ncbi.nlm.nih.gov/pubmed/27957427
http://dx.doi.org/10.1016/j.eucr.2016.11.005
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