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;
93 Cards in this Set
- Front
- Back
What is the most important aspect of studying tumors for clinicians?
|
Staging
|
|
What are 2 other ways of studying tumors that are of more importance to the pathologist?
|
-Histologic type
-Grading |
|
What are the 2 broad categories of Kidney Tumors?
|
-Benign
-Malignant |
|
What are the 3 BENIGN kidney tumors?
|
RAO
-Renal papillary adenoma -Angiomyolipoma -Oncocytoma |
|
What are 2 subcategories of Malignant Kidney tumors?
|
-Renal cell carcinomas
-Urothelial tumors of the Renal Pelvis |
|
What are 4 subclasses of Renal cell Carcinoma?
|
-Clear cell
-Papillary -Chromophobe -Collecting duct |
|
How are Renal Papillary adenomas different from Papillary type carcinomas?
|
Just their size - less than 3cm
|
|
What is the gross appearance and color of papillary adenomas or carcinomas?
|
-Well circumscribed
-Yellow-gray |
|
What does >3cm size in a papillary adenoma indicate?
|
Metastatic potential - malignancy
|
|
How are Renal papillary adenomas treated clinically?
|
Just like papillary carcinomas - as early cancer; resect it.
|
|
What are the 3 components of Angiomyolipomas?
|
-Blood vessels
-Smooth muscle -Fat |
|
What condition are angiomyolipomas found in, and what % of these patients?
|
20-50% of patients with Tuberous Sclerosis
|
|
What is Tuberous sclerosis?
|
Tumors in the Cerebral cortex
|
|
So what are 4 symptoms of Tuberous sclerosis?
|
-Skin tubors
-Epilepsy -Angiomyolipomas -Mental retardation |
|
How are Oncocytomas treated?
|
With just partial nephrectomy instead of complete.
|
|
Why are Oncocytomas just treated with partial nephrectomy?
|
Because metastases are RARE
|
|
What color are Oncocytomas?
|
Tan or mahogany brown
|
|
What do the cells that make up OncOcytOmas look like?
|
Large and round with large nucleOli
|
|
Why are Oncocytomas BROWN, and why do their large cells have granular cytoplasm on lite microscopy?
|
Because of numerous mitochondria
|
|
How can the mitochondria be best seen?
|
With EM
|
|
What % of all visceral cancers are malignant renal tumors?
|
1-3%
|
|
What type of malignancy are 85% of all renal malignant tumors?
|
Renal cell carcinomas
|
|
What is the other 15%?
|
Urothelial carcinoma of the renal pelvis
|
|
What is the predominant age at which renal cancer is seen and what is the M:F ratio?
|
-60-70's
-2-3:1 - more in males |
|
What are 7 risk factors for renal malignancy?
|
HOSECUT
-Hypertension -Obesity esp in women -Smoking -Exposure to carcinogens -CRF and Acquired cystic dis -Unopposed estrogen therapy -Tuberous sclerosis |
|
What is acquired cystic disease really?
|
The cysts that develop for no known reason after hemodialysis in ESRD
|
|
So what 3 renal diseases can lead into renal malignancy?
|
-Chronic renal failure
-Acquired cystic ESRD -Tuberous sclerosis |
|
What are the 2 genes to remember with Kidney tumors?
|
-Von hippel lindau
-MET protooncogene |
|
What chromosome is VHL on? How does it lead to cancer?
|
3p - normally a tumor suppressor; when LOST leads to cancer
|
|
What chromosome is the MET protooncogene on? How does it lead to cancer?
|
Ch' 7 - it is a protooncogene that gets ACTIVATED to cause cancer.
|
|
When the Von hippel lindau gene on Ch' 3p is lost what types of cancer develop?
|
Sporadic and Familial CLEAR CELL RCC
|
|
When the MET protooncogene on Ch' 7 is activated, what types of cancer develop?
|
Sporadic and familial PAPILLARY RCC
|
|
What is the general gross appearance of most renal cell carcinomas? Where are they located most commonly?
|
-Well circumscribed masses
-In UPPER pole |
|
What color are Renal cell carcinomas? Why?
|
Yellow - lipid
|
|
What is a common progression in development of Papillary carcinomas?
|
1. ESRD on dialysis
2. Acquire Cysts 3. Cysts -> papillary adenomas 4. Papillary adenomas turn into Papillary carcinomas |
|
What are the 2 main differences between RCC and Urothelial type carcinomas?
|
RCC = yellow and in cortex
Uro = tan/brown and in medulla or renal pelvis |
|
What is the architecture of the RCC's of CLEAR CELL type?
|
Solid to trabecular to tubular
|
|
What is the architecture of the RCC's of PAPILLARY type?
|
Papillary fronds with foam cells within their cores
|
|
What is a prominent finding in
-Clear cell RCC -Papillary RCC |
Clear cell = VASCULATURE
Papillary = Psammoma bodies |
|
What are the cytoplasms of cells like in both RCC of clear cell and papillary types?
|
Abundant and clear to Granular
|
|
What gives the granular appearance of the cells?
|
Abundant mitochondria
|
|
What is the architecture of Chromophobe type RCC? What do the cells look like?
|
Solid sheets of cells - have HPV effect of perinuclear halo and pale eosinophilia
|
|
What is the architecture of Collecting Duct type RCC?
|
Irregular channels of cells
|
|
What do the cells look like and what do they do in CD type RCC?
|
-Very atypical
-Hobnail |
|
What is Hobnailling?
|
Protruding into the lumen space
|
|
What does Sarcomatoid de-differentiation in any histologic type of RCC do?
|
Worsens prognosis a lot
|
|
What is Sarcomatoid de-differentiation?
|
The appearance of spindle cells
|
|
What is the CLASSIC triad of clinical features of RCC?
|
-CVA pain
-Palpable mass -Hematuria |
|
What % of cases GET this classic triad of CVA pain, palpable mass, and hematuria?
|
Only 10%
|
|
What is the most COMMON symptom of renal malignancy?
|
Hematuria
|
|
What 2 features of the hematuria of malignancy help differentiate it from nephritic syndrome?
|
-Microscopic (not gross)
-Intermittent |
|
So what is HPVeffect seen in?
|
Chromophobe type RCC
|
|
What are renal cell carcinomas very prone to give rise to?
|
Paraneoplastic syndromes!
|
|
What is a common paraneoplastic syndrome RCC can cause? Why?
|
Polycythemia - due to EPO
|
|
What structure in the kidney do RCC's have a HIGH propensity to involve?
|
The renal VEIN!
|
|
What does the involvement of the renal vein allow for renal cell carcinoa to do?
|
Metastasize widely and to often ODD sites
|
|
What are the 2 most common sites for renal malignancy to metastasize to?
|
-Lungs
-Bone |
|
What are 3 treatments for kidney tumors?
|
-Nephrectomy
-Partial nephrectomy -Cryoablation |
|
What % of renal malignancies are Urothelial carcinomas of the Renal Pelvis?
|
Only 5-10%
|
|
What are Urothelial carcinomas similar to?
|
Those of the urinary tract and bladder.
|
|
What % of Urothelial carcinomas (UC) of the renal pelvis have concomitant or pre-existing BLADDER UC?
|
50%
|
|
What drug abuse is UC associated with?
|
Analgesic abuse
|
|
How does the size/location of UC compare to RCC?
|
-UC is usually smaller and in the pelvis or calyces.
-RCC is larger and in the cortex |
|
Why do urothelial cancers tend to present EARLIER?
|
Bc they can break off and cause hematuria - with or without pain.
|
|
How does the prognosis of urothelial cancers compare to RCC? Why?
|
Worse - because they can become highly invasive.
|
|
What is the 5-yr survival for low grade, superficial UC?
|
50-70%
|
|
What is the 5-yr survival for high grade invasive UC?
|
Only 10% :(
|
|
What are the 2 types of Urinary BLADDER and Ur. TRACT tumors, based on origin?
|
95% - Epithelial origin
5% - Mesenchymal origin |
|
What are 4 types of epithelial tumors of the Ur. Bladder and Tract?
|
-SCC
-Adenocarcinoma -Small cell -Mixed |
|
What are 2 types of mesenchymal tumors?
|
-Leiomyomas
-Sarcomas |
|
What Sarcoma would be seen in Adults with urinary bladder or ur. tract sarcoma?
|
Leiomyosarcoma - smooth muscle
|
|
What Sarcoma would be seen in Children with urinary bladder or ur. tract sarcoma?
|
Rhabdomyosarcoma - skeletal mm
|
|
What are the 2 main features to be concerned with in looking at tumors of the Ur. Bladder and Tract?
|
-Papillary vs Flat
-Invasive or Not |
|
What is Papillary?
|
Protruding out
|
|
What is easier to detect on microscopic exam? Why?
|
Flat lesions - Papillary tumors may just be artifact.
|
|
How would Papillary tumors be detected best?
|
By cystoscopic examination
|
|
How many cellular layers are normal in urothelium?
|
Up to 7
|
|
What are the 4 grades of Urothelial tumors?
|
1. Urothelial papilloma
2. Urothel neoplasm of LMP 3. Papillary UC low grade 4. Papillary UC high grade |
|
What feature is seen in just Urothelial papilloma?
|
Increased cellular layers >7
|
|
What feature is seen in just PUNLMP (papillary urothelial neoplasm of LMP)?
|
Even more cells but no atypia
|
|
What 2 features are characteristic of Low grade UC in the urinary bladder/tract?
|
-Minimal but DEFINITE nuclear atypia
-A few mitotic figures |
|
What makes High grade UC distinct?
|
-FRANK nuclear atypia
-Many mitotic figures |
|
What happens to the architecture in high grade UC?
|
-Disarray
-Loss of polarity |
|
What is the next step in cancer progression after high grade urothelial carcinoma?
|
Carcinoma in situ
|
|
What is CIS always?
|
-Flat
-Hyperchromatic |
|
What infection is SCC of the urinary bladder/tract associated with?
|
Schistosoma haematobium
|
|
What embryonic remnant is prone to developing Adenocarcinoma of the urinary bladder/tract?
|
Urachus
|
|
What type of lesion is Adenocarcinoma of the urachus typically?
|
A wall lesion that grows OUT from the serosa; not the mucosa.
|
|
What is Cystitis cystica et glandularis?
|
Cystic Outpouchings of urothelium that often contain mucin-producing cells.
|
|
What are 2 things that Cystitis cystica et glandularis is commonly caused by?
|
-Transurethral resection to remove urinary tract tumors
-Post-BGC granulomatous |
|
What will be seen in cystitis cystica et glandularis following transurethral resection of urinary tract tumors? on histology?
|
Spindle cell nodules
|
|
What will be seen in Post-BGC granulomatous cystitis?
|
Granulomas just like you would see anywhere else.
|
|
Is the postop spindle cell nodule in cystitis cystica et glandularis a neoplasm?
|
No - it is a reactive formation following the TRAUMA of transurethral resection.
|