• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/44

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

44 Cards in this Set

  • Front
  • Back
Embryonal renal neoplasms
Nephroblastoma
Congenital mesoblastic nephroma
Solitary multilocular cyst
Renal cell carcinoma epidemiology
1-3% of adult malignancies
>85% of kidney malignancies
M 2 > 1 F
Peaks incidence in 60s
Risk factors for RCC?
Urban environment
Tobacco
Chemical agents
Old school presentation of renal cell carcinoma
Hematuria
Pain
Flank mass

Now only 15% of presentations
Many are found incidentally
Systemic signs possible in RCC
Anemia
Fever
Hepatic dysfnc
Amyloidosis
RCC paraneoplastic syndromes
polycythemia - epo
hypercalcemia - PTHRP
HTN - renin
Cushings - ACTH-like
Gross pathology of RCC
Mostly unilateral
Anywhere in renal parenchyma
Symptoms related to size

If symptomatic
Avg is 5-8 cm
40% through capusule
35% in renal vein
40% with distant mets

Variegated appearance
Yellow to gray
Hemorrhage
Clear cell RCC
Histology
Majority of RCC

Fine but abundant capillary network
Clear from vacuoles full of neutral lipids and glycogen
Sarcomatoid differentiation in RCC
Cells are elongated
Spindle like

Poor prognostic
Staging RCC
I - contained in capsule
II - perinephric fat
III - into renal vein, IVC, regional nodes
IV - adjacent organs or distant mets
Natural history of RCC
Unpredictable

May be slow or rapid growing
Periods of quiescence

Rare spontaneous regression

Oligometastatic disease my be curable
Metastatic locations for RCC
Lung - 50%
Bone -30%

LNs
Liver
Adrenal
Brain
Renal adenomas
Same histology as RCC
Just < 2-3 cms
Less likely to be malignant
Nephroblastoma epi
AKA Wilms
Rare tumor
50% in < 3 years old
90% in < 10 years

Male = female

Associated with sporadic aniridia, hemihypertrophy, others
Gross pathology of neprhoblastoma
Large
Pseudoencapsulated
Encephaloid -- looks like brain
Histology of nephroblastoma
Three types of cells
Stroma
Epithelium (tubules/glomeruli)
Blastema cells - primitive cells
Nephroblastoma pathogenesis
Persistent remains of metaneprhic blastema

These multipotent nests of cells in fetal kidney usually disappear by 4-5 months gestation
Treating nephroblastoma
Surgery
XRT
Chemo - vincristine, daptomycin
Prognostics for nephroblastoma
All have a good prognosis ~90% cure in all comers

Poor prognostics:
Older pt
Higher stage
within stg 1--anaplastic histo
Anaplasia in RCC
Defines a pop of cells likely to be resistant

Multipolar mitotic features
Big nuclei
Urothelial tumors
Arising from epi anywhere along the tract
Similar histo/staging/prognosis
Multicentricity of urothelial tumors
More than one focus of tumor concurrently
Field change of dysplasia

Important for surgical decisions
Bladder cancer
Presents as hematuria, pain, frequency, dysuria
M 5 > 1 W
60-80 year olds

Diagnose w/ cytology or cystoscopy
Risk factors for developing bladder ca
Smoking

Aromatic amines (dye industry)
Beta-naphthylamine
4-Aminobiphenyl
Chlornaphazine

Suspected: Shistosomiasis, stones, arsenic
Structures of urothelial lesions
Papillary - majority
In situ (flat)

Either can invade, but in situ does more frequently
Histology of low grade papillary urothelial carcinoma
Fine, delicate, non-fused papillary fronds with uroepithelium
Relatively evenly spaced tumor cells
Histology of high grade papillary urothelial carcinoma
Papillary fronds are bulky and overlapping
Tumor cells are dark, enlarged, disordered in maturation
Bladder cancer prognosis
Stage (duh)
but also correlates well with tumor grade
Treating bladder cancer
Topicals - BCG, thiotepa, mitomycin C

XRT

Surgery - transuretheral or radical cystectomy (includes urethrectomy, distal ureterectomy) with conduit

Chemo
How often are ureter/urethra involved in bladder cancer
15% of time for each
Upper tract urothelial cancers
1/4 as prevalent as RCC
60s-70s, M 5 > 1 F

Hematuria

Nephrouterectomy with bladder cuff rxn
What malformation coexists with polycystic kidneys?
Liver cysts (33%)
Berry aneurysms (15%)
What's associated with juvenile polycystic kidneys?
Congenital hepatic fibrosis
Horseshoe kidney
Failure to to separate poles of kidney
Leads to a failure to rotate into normal position
hilum lies anteriorly
Medullary sponge kidney
Cysts at tips of papillae
Pretty benign
Dysplastic kidney histology
Scattered cysts
Disorganized parenchyma
Cartilage common
Medullary cystic kidney disease
Dysplastic kidney disease
Cysts confined to medulla
Dominant vs recessive PKD on pathology
Dominant - big, bulging cysts

Juvenile - cyst filled kidney, more internal, enlongated, linear pattern
Most common presentation of renal dysplasia
Cystic kidney in kid
Renal adenomcarcinoma aka
Renal cell carcinoma
5 year prognosis in RCC?
50%
Presentation of nephroblastoma
Abdominal mass in child
Uremic medullary cystic kidney disease
Rare
Adolescents and young adults
Cysts at cortiocomedullary jct

Severe uremia
Developmental things that can go wrong with the ureteric bud
Failure to develop - agenesis
Abl position of wolffian - ureterocele, diverticula, ectopic ureter
Splitting - bifid, duplex ureters
Excessive absorption into bladder - increased reflux