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

A

better

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 …

A

kidney

24
Q

hereditary papillary carcinoma
inheritance?
manifests as?
mutations in…

A

autosomal dominant

mutliple bilateral tumors

MET protooncogene

25
Q

T indicates …
N indicates …
M indicates …

A

T = tumor’s size and spread to nearby tissues

N = cancer spread to nodes near kidney

M = metastasize

26
Q

95% of urinary tract tumors are of ___ origin

5% of urinary tract tumors are of ___ origin

A

epithelial

mesenchymal

27
Q

most epith tumors are composed of ___ cells and also called ___

A

urothelial (transitional) cell

28
Q

benign neoplasms of urinary tract are represented by small tumors of ___ origin

A

mesenchymal

29
Q

2 most common benign neoplasms

A

fibroepithelial polyps

leiomyomas

30
Q

fibroepithelial polyps presents as ____

more commonly in the ___

A

small mass project into lumen

left ureter > right

31
Q

80% btwn 590-80
smokers
industrial exposures and radiation

A

transitional cell neoplasm

32
Q

> 90% of tumors from urinary tract including squamous cell and adenocarcinoma

A

transitional cell neoplasms

33
Q

presents with hematuria and dysuria, freq, urgency

A

transitional cell neoplasm

34
Q

arises from calyces, pelvis, ureters, bladder, urethra, and extend to pelvic sidewalls and go to lungs, bones, liver

A

transitional cell neoplasm

35
Q

tumor causing ureteral obstruction –> hydroenphrosis (unilateral or bilat)

A

transitional cell neoplamss

36
Q

filling defect in urinary tract on imaging

purely papillary to nodular or flat

A

transitional cell neoplasm

37
Q

therapy for transitional cell neoplasm

A

1) BCG
2) electrocautery
3) surgery