Tumors of Kidney and Urinary Tract Flashcards

1
Q

benign tumors rarely ___

A

cause problems

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2
Q

malignant tumors order of prevalence

A

1) RCC
2) Wilsm
3) urothelial tumors of calyces and pelvis

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3
Q

Benign tumors

1) located in cortex
2) small (5 mm)
3) surgically removed

A

renal papillary adenoma

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4
Q

Benign tumors
1) fibrous
2)

A

renal fibroma/hamartoma

renomedullary interstitial cell tumor

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5
Q

Benign tumors

1) vessels, smooth muscle, fat
2) 25-50% in patients with tuberous sclerosis

A

angiomyolipoma

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6
Q

Benign tumors

1) eosinophilic epith cells
2) numerous mitochondria
3) 5-15% of all renal neoplasmas
4) in families

A

oncocytoma

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7
Q

Benign tumors

1) rare
2) metasizes

A

metanephric adenoma

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8
Q

1) most common RCC
2) hematuria, renal mass on imaging
3) in renal cortex –> invades renal vein –> IVC
spread to nodes, lungs

A

clear cell carinoma

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9
Q

imaging

1) ball mass of renal cortex
2) engorged renal vein + IVC

A

clear cell carcinoma

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10
Q

histology

1) single tumor, spherical
2) 3 cell types = clear, granular spindle

A

clear cell RCC

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11
Q

familial assoc with VHL (4%

sporadic 95%

98% lose sequences on short arm chromosome 3

A

clear cell carcinoma

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12
Q

tumor grades 1-2 have ___ prognosis compared to tumors 3-4

A

better

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13
Q

10-15% of RCC
Pathology
Frequently multifocal (multi-cell)
papillary growth pattern

A

papillary carcinoma

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14
Q

genetics
familial + sporadic
NOT 3p deletions
Trisomies 7, 16, 17, loss of Y

A

papillary carcinoma

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15
Q

mutated gene on chromosome 7 (MET locus = protooncogene for tyrosine kinase receptor)

A

papillary carcinoma

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16
Q

5% of renal cell cancers

prominent cell membranes
pale eosinophilic cytoplasm
halo around nucleus

A

chromophobe renal carcinoma

17
Q

genetics
multiple chromosome losses
hypodiploidy

from intercalated cells

A

chromophobe renal carcinoma

18
Q

chromophobe renal carcinoma has a ___ prognosis compared to clear cell and papillary cancers

19
Q

1% of renal epithelial neoplasms
arises from collecting duct cells in medulla

nests of malignant cells in fibrotic stroma (medulla)

A

collecting duct carcinoma

20
Q

best method for prolonging patient survival with collecting duct carcinoma

A

early detection

21
Q

4% of renal cancers

names of familial RCC

A

1) VHL syndrome
2) hereditary familial clear cell carinoma
3) hereditary papillary carcinoma

22
Q

VHL symptoms

develop ….

A

hemangioblastomas of cerebellum and retina

renal cysts and bilateral renal cell carcinomas

23
Q

hereditary clear cell carcinoma confined to …

24
Q

hereditary papillary carcinoma
inheritance?
manifests as?
mutations in…

A

autosomal dominant

mutliple bilateral tumors

MET protooncogene

25
T indicates ... N indicates ... M indicates ...
T = tumor's size and spread to nearby tissues N = cancer spread to nodes near kidney M = metastasize
26
95% of urinary tract tumors are of ___ origin 5% of urinary tract tumors are of ___ origin
epithelial mesenchymal
27
most epith tumors are composed of ___ cells and also called ___
urothelial (transitional) cell
28
benign neoplasms of urinary tract are represented by small tumors of ___ origin
mesenchymal
29
2 most common benign neoplasms
fibroepithelial polyps leiomyomas
30
fibroepithelial polyps presents as ____ more commonly in the ___
small mass project into lumen left ureter > right
31
80% btwn 590-80 smokers industrial exposures and radiation
transitional cell neoplasm
32
> 90% of tumors from urinary tract including squamous cell and adenocarcinoma
transitional cell neoplasms
33
presents with hematuria and dysuria, freq, urgency
transitional cell neoplasm
34
arises from calyces, pelvis, ureters, bladder, urethra, and extend to pelvic sidewalls and go to lungs, bones, liver
transitional cell neoplasm
35
tumor causing ureteral obstruction --> hydroenphrosis (unilateral or bilat)
transitional cell neoplamss
36
filling defect in urinary tract on imaging purely papillary to nodular or flat
transitional cell neoplasm
37
therapy for transitional cell neoplasm
1) BCG 2) electrocautery 3) surgery