Primary Amyloidosis of the Urinary Bladder

Amyloidosis is a systemic disease that usually occurs in the gastrointestinal tract or in muscular or adipose tissue. Primary amyloidosis of the urinary bladder is a rare disease that can mimic bladder cancer on cystoscopic examination as well as in its clinical presentation of painless gross hematu...

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Main Authors: Chao-Yuan Huang, Kuo-How Huang, Jun Chen, Yeong-Shiau Pu
Format: Article
Language:English
Published: Elsevier 2006-01-01
Series:Journal of the Formosan Medical Association
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S0929664609603399
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spelling doaj-397da277ffce45319faefb87cee8d1592020-11-24T23:50:55ZengElsevierJournal of the Formosan Medical Association0929-66462006-01-01105216416710.1016/S0929-6646(09)60339-9Primary Amyloidosis of the Urinary BladderChao-Yuan HuangKuo-How HuangJun ChenYeong-Shiau PuAmyloidosis is a systemic disease that usually occurs in the gastrointestinal tract or in muscular or adipose tissue. Primary amyloidosis of the urinary bladder is a rare disease that can mimic bladder cancer on cystoscopic examination as well as in its clinical presentation of painless gross hematuria. This report describes a 49-year-old male with repeated painless gross hematuria, who underwent transurethral resection of a suspected bladder tumor. Pathologic examination revealed papillary urothelial hyperplasia with vascular ectasia and no signs of malignancy. Massive gross hematuria occurred 2.5 years later. Cystoscopy showed multiple papillary lesions with yellowish-brown submucosal plaques on the posterior bladder wall. A second transurethral tumor resection was performed and histologic examination revealed plasma cell infiltration and eosinophilic amorphous deposits in the subepithelial stroma and vascular wall. The deposits were positive for Congo red and apple-green birefringence under polarized light examination but negative for Masson's trichrome stain, indicating that they were not fibrotic in nature. Hence, the diagnosis of amyloidosis of the urinary bladder was confirmed. Screening for amyloidosis was negative in other organ systems and the patient has remained disease-free up to the last follow-up 4 years after the second transurethral resection. Amyloidosis should be considered in the differential diagnosis of patients with recurrent hematuria who have symptoms characteristic of bladder cancer but negative pathologic study for malignancy. Correct diagnosis relies on clinical alertness and the use of a special staining technique during pathologic examination.http://www.sciencedirect.com/science/article/pii/S0929664609603399amyloidhematuriaurothelial carcinoma
collection DOAJ
language English
format Article
sources DOAJ
author Chao-Yuan Huang
Kuo-How Huang
Jun Chen
Yeong-Shiau Pu
spellingShingle Chao-Yuan Huang
Kuo-How Huang
Jun Chen
Yeong-Shiau Pu
Primary Amyloidosis of the Urinary Bladder
Journal of the Formosan Medical Association
amyloid
hematuria
urothelial carcinoma
author_facet Chao-Yuan Huang
Kuo-How Huang
Jun Chen
Yeong-Shiau Pu
author_sort Chao-Yuan Huang
title Primary Amyloidosis of the Urinary Bladder
title_short Primary Amyloidosis of the Urinary Bladder
title_full Primary Amyloidosis of the Urinary Bladder
title_fullStr Primary Amyloidosis of the Urinary Bladder
title_full_unstemmed Primary Amyloidosis of the Urinary Bladder
title_sort primary amyloidosis of the urinary bladder
publisher Elsevier
series Journal of the Formosan Medical Association
issn 0929-6646
publishDate 2006-01-01
description Amyloidosis is a systemic disease that usually occurs in the gastrointestinal tract or in muscular or adipose tissue. Primary amyloidosis of the urinary bladder is a rare disease that can mimic bladder cancer on cystoscopic examination as well as in its clinical presentation of painless gross hematuria. This report describes a 49-year-old male with repeated painless gross hematuria, who underwent transurethral resection of a suspected bladder tumor. Pathologic examination revealed papillary urothelial hyperplasia with vascular ectasia and no signs of malignancy. Massive gross hematuria occurred 2.5 years later. Cystoscopy showed multiple papillary lesions with yellowish-brown submucosal plaques on the posterior bladder wall. A second transurethral tumor resection was performed and histologic examination revealed plasma cell infiltration and eosinophilic amorphous deposits in the subepithelial stroma and vascular wall. The deposits were positive for Congo red and apple-green birefringence under polarized light examination but negative for Masson's trichrome stain, indicating that they were not fibrotic in nature. Hence, the diagnosis of amyloidosis of the urinary bladder was confirmed. Screening for amyloidosis was negative in other organ systems and the patient has remained disease-free up to the last follow-up 4 years after the second transurethral resection. Amyloidosis should be considered in the differential diagnosis of patients with recurrent hematuria who have symptoms characteristic of bladder cancer but negative pathologic study for malignancy. Correct diagnosis relies on clinical alertness and the use of a special staining technique during pathologic examination.
topic amyloid
hematuria
urothelial carcinoma
url http://www.sciencedirect.com/science/article/pii/S0929664609603399
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AT kuohowhuang primaryamyloidosisoftheurinarybladder
AT junchen primaryamyloidosisoftheurinarybladder
AT yeongshiaupu primaryamyloidosisoftheurinarybladder
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