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49 Cards in this Set
- Front
- Back
RCC, especially clear cell invade renal ____ and
obstruct it. |
vein
|
|
RCC may be sporadic, familial or associated with
____ (familial hemangiomas) |
VHL
Von Hippel Lindau |
|
Chromosome of RCC
|
3p-
|
|
Diseases associated with RCC
|
–von Hippel-Lindau disease
–Tuberous Sclerosis –Autosomal dominant polycystic kidney disease –Acquired cystic renal disease –? familial RCC |
|
most common renal tumor in adults
|
clear cell carcinoma
|
|
What is in the cytoplasm of clear cell carcinoma
|
glycogen
use PAS stain |
|
gross appearance of chromophil RCC
|
variable, may have papillary or friable, cut surface
|
|
Color of clear cell vs color of chromophobe RCC
|
clear: yellow
chromophobe: brown |
|
Stain specific for iron colloids of chromophobe RCC
|
Hale's
|
|
Renal cell carcinoma. A, Clear cell type, B, Papillary type. Note the
papillae and foamy macrophages in the stalk. C, Chromophobe type. |
Renal cell carcinoma.
A?B?C? |
|
Collecting Duct carcinoma Aka
|
Medullary carcinoma
|
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Collecting Duct carcinoma:
Malignant cells with a ____ pattern lining irregular glandular spaces |
hobnail
|
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Juxtaglomerular Cell Tumor AKA("__?__")
|
Reninoma
|
|
EM of JGA tumor shows what in the cytoplasm
|
Renin granules
|
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Friable tumors that obstruct
the renal pelvis Males 10:1 Much less common than urothelial cellthe bladder. |
Urothelial cell carcinoma
|
|
WAGR: problems
|
Wilm’s tumor,aniridia (congenital absence or
partial absence of the iris), GU malformations, and mental retardation |
|
Beckwith-Wiedeman syndrome
|
congen exomphalos, macroglossia, gigantism
(80% of patients demonstrate genotypic abnormalities of 11p15.5) |
|
Patients often have aniridia, hemihypertrophy, and/or
rests of undifferentiated blastema. |
Wilm’s tumor
|
|
–Autosomal dominant polycystic KD
Why would this pt have "the worst headache of their life?" |
subarachnoid hemorrhage due to burst berry aneurysm
|
|
what is the gross difference b.w recessive and dominant polycystic kidney disease?
|
no cysts on the outside of kidney in recessive disease
|
|
Usually it is just a radiologist's curiosity.
• Sometimes stones form in the "cysts", and this entity is in the "differential" of chronic back pain |
Medullary sponge kidney
|
|
The hereditary forms of this disease include three diseases coded
by NPHP1 ("nephrocystin"), NPHP2, and NPHP3, which are the most common causes of endstage renal disease in children and young adults |
Uremic medullary cystic
disease / "nephronophthisis” |
|
Bridge over water
|
uterine arteries go over ureters
|
|
Problem causing pyelonephritis in UTI
|
Vesicoureteral
reflux (defect in intravesical portion of ureters) |
|
Intrinsic Narrowing or occlusions of ureters
|
a. Normal anatomical sites of narrowing
b. Calculi (intrinsic) -most frequent cause of obstruction c. Stricture (intrinsic) -trauma, inflammatory d. Tumors (intrinsic) e. Blood clot (intrinsic) |
|
condition that can result in hydroureter
|
Pregnancy
|
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Extrinsic compression of ureters
|
i Tumors (benign or malignant) common in cervix
cancer –ii. Pregnancy -can result in hydroureter –iii. Sclerosing retroperitonitis (Retroperitoneal fibromatosis) –iv. Endometriosis |
|
Urothelium
normally consists of 4 to 6 layers of cells. The uppermost layer consists of _______ cells (not well seen in this image) which may have irregular hyperchromatic nuclei. |
umbrella
|
|
-developmental failure of anterior abdominal
wall. May be repaired surgically. |
Exstrophy
|
|
Increased frequency, lower abdominal pain and dysuria.
|
Cystitis
|
|
Schistosomiasis causes what kind of cancer
|
squamous cell cancer of the bladder
|
|
Predisposing conditions for cystitis
|
– i. Coitus (female)
– ii. Prostatic hyperplasia (male) – iii. D.M. –iv. Stones –v. Diverticula –vi. Tumors –vii. Pregnancy –viii. Neuronal disorders (spinal cord injury, autonomic dysfunction) – ix. Catheterization and surgery –x. Radiation |
|
bladder infection assoc with long term use of antibiotics
|
Candida
|
|
organism infection causing cystitis
|
• i. Gram negative rods (100,000 organisms/cc)
i.e. E.coli, Proteus, Klebsiella • ii. T.B. • iii. Schistosomiasis • iv. Candida -usually on long-term antibiotics |
|
Special types of cystitis
|
Malakoplakia
Ulcerative interstitial cystitis. Cystitis related to cytotoxic drugs and radiation |
|
c. Michaelis-Gutman body is assoc with what?-
|
Malakoplakia
|
|
What is Michaelis-Gutman body?
|
Probably calcified
phagolysosomes of macrophage containing bacterial debris. Most are associated with chronic E. coli or Proteus infections |
|
Inflammation and
fibrosis throughout all layers of bladder wall; mainly female. Cause unknown; perhapsautoimmune. |
Ulcerative interstitial cystitis.
|
|
CARCINOMA OF THE
BLADDER is usually what type |
Usually papillary
|
|
_____ carcinoma is the most frequent malignant tumor of
the urinary tract. |
Bladder
|
|
location dispersion bladder carcinoma
|
84% occur on the lateral & posterior walls of the bladder &
40% occur in the trigone. |
|
______- dye used in rubber and cable industries. 50 fold
increased in bladder cancer in exposed workers. |
Aniline
|
|
Beta naphthylamine, 4-amino biphenyl, 4-nitro biphenyl
and 4,4 diamino-biphenyl, and _____ tar can cause tumors in animals. |
tobacco
|
|
Chronic bladder infections and calculous disease or
Schistosoma hematobium (North Africa) are etiologic in _______ cell type of bladder cancer. |
squamous
|
|
___________ is
the single most important factor in predicting the ultimate prognosis of a particular lesion and is the basis of staging bladder cancer. |
Depth of penetration of the tumor into the bladder wall
|
|
Majority of tumors (70%) are what type?
|
Papillary CA low grade:
|
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Type of tumor that is Essentially benign. May recur but rarely invade
|
Papilloma / LMP:
|
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Type of tumor Often widespread, and one step from invasion.
|
Flat urothelial / CIS :
|
|
Type of tumor Associated with chronic irritation -stones,
|
Squamous cell Ca
(70% dead in one year ) |