Difference between revisions of "Urinary bladder amyloidosis"
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Congo red staining and polarization confirm the presence of amyloid. | Congo red staining and polarization confirm the presence of amyloid. | ||
Primary bladder amyloidosis is rare; systemic causes of amyloidosis should | |||
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Revision as of 18:20, 2 October 2015
Urinary bladder amyloidosis, more formally primary urinary bladder amyloidosis, is a rare benign condition of urinary bladder that can mimic cancer of the urinary bladder.[1]
General
- Primary bladder amyloidosis is rare - approximately 200 reported cases as of 2014.[1][2]
- Systemic amyloidosis should be excluded.[2]
- May clinically mimic bladder cancer.[1]
Gross
- Urinary bladder wall thickening.[1]
Microscopic
Features:
- Lamina propria with amyloid (amorphous, paucicellular, pink material on H&E - classically "cracked").
Stains
- Congo red +ve.
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Urinary Bladder, Transurethral Resection: - Urothelial mucosa with amyloidosis and mild chronic inflammation. - Benign muscularis propria present. - NEGATIVE for urothelial carcinoma in situ. - NEGATIVE for malignancy. Comment: Congo red staining and polarization confirm the presence of amyloid. Primary bladder amyloidosis is rare; systemic causes of amyloidosis should be considered.
See also
References
- ↑ 1.0 1.1 1.2 1.3 Kobayashi, T.; Roberts, J.; Levine, J.; Degrado, J. (2014). "Primary bladder amyloidosis.". Intern Med 53 (21): 2511-3. PMID 25366012.
- ↑ 2.0 2.1 Schou-Jensen, KS.; Dahl, C.; Pilt, AP.; Azawi, NH. (Oct 2014). "Amyloidosis in the bladder: three cases with different appearance.". Scand J Urol 48 (5): 489-92. doi:10.3109/21681805.2014.920414. PMID 24857645.