Exam 2- Tumors Flashcards

1
Q

What is the most common benignrenal cancer

A

renal papillary adnoma

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2
Q

What are the benign cancers of the kidneys

A

renal papillary adenoma, angiomyolipoma, oncocytoma, renal fibroma or hamartoma
juxtaglomerular cell tumor
mesenchymal tumores

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3
Q

What is the size of a benign ademoa

A

<1 cm

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4
Q

what are ademoas that are >1cm in diameter

A

low grade RCC

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5
Q

What is the gross appearance or papillary ademoas

A

cortical, discrete, yellow gray, small and there may be multiple of them
may have psammoma bodies
acidophilic cytoplasm

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6
Q

what genetic mutation is assoc with renal papillary ademoa

A

trisomy 7 and 17

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7
Q

What disease has 25-50% patients present with angiomyolipomas

A

tuberous sclerosis

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8
Q

What is tuberous sclerosis and what is mutation involved

A

TSC1 or 2 (tumor suppressor genes
autosomal dominant
tumores or lesions of brain(mental retardation), skin, kidney, hear, lungs and eyes
lisch nodules

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9
Q

Angiomyolipomas greatest risk factor is what

A

susceptible to spontaneous hemorrhage, massive retroperitoneal hemorrhage and shock

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10
Q

Where do oncocytomas arise from

A

type A intercalated cells of renal cortical collecting ducts

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11
Q

what is the morphology on oncocytomas

A
epithelial tumor with large eosinophilic cells, large round nuclei
numerous mitochondria
large tan or brown mahogany color. 
get grow to 12 cm
stellate scar
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12
Q

What is the familial association with oncocytomas

A

familial 10 q deletion with multicentricity and b/l

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13
Q

What are oncocytomas confused with

A

RCC , non clear cell

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14
Q

What age gorup are oncocytomas Dx in

A

adults.

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15
Q

What is the population of tuberous sclerosis and renal angiomyolipoma

A

middle aged females

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16
Q

What is the most common adult renal malignant tumor

A

RCC

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17
Q

what population is RCC seen mostly in

A

60-80 yrs old male to femal 2:1 equal distribution racially

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18
Q

what does RCC arise from

A

renal tubular epithelium, adenocarcinoma

19
Q

what are the risk factors assoc with RCC

A

SMOKING

HTN obesity, estrogens, asbestos, chronic renal disease, tuberous sclerosis, acquired cystic disease

20
Q

What is the hereditary form of RCC

A

autosomal dominant
younger patients
VHL syndrome develop b/; hereditary clear cell carcinoma or hereditary papillary carcinoma

21
Q

What is the most common type of RCC

A

clear cell
clear granular cytoplasm
non papillary
95% sporadic

22
Q

what is the mutation seen with clear cell carcinoma familial

A

loss of sequences on short arm of chromosome 3. deletions or translocations
this is the VHL tumor supressor gene

23
Q

What is Birt Hogg Dube syndrome and what type inheritance

A

folliculin gene mutation, autosomal dominant

skin pulmonary and renal tumors

24
Q

What type of mutation is seen in papillary carcinoma

A

trisomy 7, 16,17 lost Y (MET oncogene)

25
A renal tumor has clear cytoplasm with papillary architecture in the medulla. and is Dx in a young patient. not clear cell or papillary. what is it?
Xp11 translocation carcinoma | collecting (bellini) duct carcinoma
26
What is the morphology of chromophobe renal carcinoma
pale eosinophilic cytoplasm, nuclear halos, arise from type B intercalated cells of renal Cx collecting ducts solid growth pattern
27
What does chromophobe renal carcinoma resemble
oncocytoma
28
where are papillary tumors clinically found
distal convoluted tubles b/l can invade renal vein, vena cava
29
What is the classic triat of RCC
hematuria (microscopic usually) CVA pain palpable flank mass
30
When RCC are Dx whats the main concern
already have metastasized
31
What are the begining symptoms of RCC
weight loss, malaise, weakness, fever
32
where does RCC metastasize to
lung, bone, regional nodes, liver, adrenal brain and unusual sites
33
Rank the types of RCC histologic types and associated prognostic value
papllary and chromophobe have better Px clear cell is moderate collecting duct, sarcamatoid and medullary have worse Px
34
What is the main mode of spread of RCC
hematogenous
35
what is another name for clear cell renal carcinoma
hypernephroma
36
What does a sarcamatoid RCC look like
spindle cells simulating mesenchymal neoplasm
37
what does collecting duct RCC look like
branching tubules lined by cuboidal cells
38
What does renal medullary RCC look like
in patient with sickle cell | poorly differentiated and heavily infiltrated with neutrophils
39
What type of cancer arises from urothelium of renal pelvis
urothelial(transitional cell) carcinoma of renal pelvis
40
50% of people with urothelial carcinomas have what other type tumor
bladder
41
what nephropathies are urothelial carcinomas assoc with
analgesic and tubulo-interstitial
42
what are signs of urothelial carcinoma
hematuria, small, may block outglow and cause hydronephrosis and flank pain
43
What is the 5 yr survival rate for urothelial carcinoma of renal pelvis
50-100% for low grade noninvasive lesions | 10% for high grade infiltrating tumors