Urinary Tract/ Bladder Disease-- Melissa* Flashcards
What type of tissue lines the lower URT (ureters, bladder, urethra)?
urothelial epithelium (Transitional epithelium)
List three sites of normal anatomical ureter narrowing:
- Ureteropelvic junction (infant obstruction common)
- Crossing at external/common iliac aa.
- Ureter/bladder junction (enter in oblique fashion)
Common finding associated with double ureter:
-Associated with duplication of renal pelvis
Population that gets urteopelvic junction obstruction?
Which side is this normally on?
What can it cause?
- # 1 Male children
- Lt»_space;> Rt–>Hydronephrosis
What is a ureteral diverticulum?
Saccular outpouching of ureteral wall
Describe what is seen with acute ureter inflammation. How does this occur?
UTI
Neutrophillic infiltrate; acute inflammatory changes
What are the 4 types of chronic ureter inflammation?
Uretritis Cystica Uretritis Folliculitis Uretritis Glandularis Intestinal Metaplasia **All will have lymphs, fibrosis, and typical chronic inflammatory changes**
Uretritis Cystica:
Definition and defying histo feature?
- Cysts deep in mucosa
- BRUNN NESTS (mucosal invaginations ) with small central clearing (1-5mm cysts)
Uretritis Folliculitis:
Definition and histo features?
-Bumps on ureter surface full of lymph tissue
Uretritis Glandularis:
What happens here?
-Ureteral tissue replaces with glandular tissue
Intestinal Metaplasia:
What happens here?
-Uroepithelium–> goblet cells
Two Benign tumors of the bladder?
Leiomyoma and polyps
What do we call malignancy of the bladder? #1 risk? With what genetic disorder might these tumors be associated?
Uroepithelial Ca.
- # 1 risk = SMOKING (also occupational exposure, analgesic nephropathy)
- Asstd with Hereditary Nonpolyposis colorectal cancer
Genetic mutation associated with HNPCC
HNPCC DNA mismatch repair gene mutation
Two general types of ureter obstructive lesions:
Can be intrinsic—calculi, strictures, tumor etc. or extrinsic—preggos, inflammation, endometriosis, etc
Two obstructive diseases of the ureter:
- Sclerosing Retroperitoneal Fibrosis
- Hydronephrosis (secondary to ureteropelvic junction obstruction)
Sclerosing Retroperitoneal Fibrosis:
Population + #1 cause?
By what is this disease mediated?
How is it treated?
- Generally idiopathic syndrome of middle to late age
- IgG4 mediated ureter fusion to retroperitoneum
- requires surgical correction
Three potential causes of sclerosing retroperitoneal fibrosis?
Three potential comorbidities with sclerosing retroperitoneal fibrosis?
- Potential causes: ergot derivatives, inflammatory syndromes (Chrons), malignancy (lymphoma)
- Possible comorbidities: mediastinal fibrosis, Sclerosing cholangitis, Riedel Fibrosing thyroiditis
Sclerosing Retroperitoneal Fibrosis:
Histo features
-Micro: Chronic inflammatory changes; EOS; +/-fat necrosis; +/-granulomas
Hydronephrosis:
What is it, who gets it, and where does it most commonly occur?
- Common complication secondary to uretopelvic junction obstruction in males
- Typically on left side (20% bilateral)
What is a bladder diverticula? Why is it dangerous?
- Congenital»_space;> Acquired invagination of bladder wall
- Possible site for tumorigenesis
Exstrophy of the bladder: what is it?
- Developmental failure of anterior abdominal and bladder wall
- Bladder extrudes lower abdominal wall