Nephrolithiasis, bladder cancer, renal cell carcinoma Flashcards

1
Q

What is Kidney stone Etiology?

A
  • Stone formation occurs when normally soluble material (Ca, PO4, uric acid) supersaturates the urine and begins the process of crystal formation.
  • It is not clear how crystals formed in the tubules become a stone, rather than being washed away by the high rate of urine flow.
  • It is presumed that crystal aggregates become large enough to be anchored ( usually at the end of the collecting ducts), and then slowly increase in size over time.
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2
Q

What are types of Nephrolithiasis?

A
-60-80% calcium stones 
(Ca oxalate > Ca phosphate)
-15% struvite 
(magnesium ammonium phosphate)
-5% uric acid (radiolucent stones)
-1-3% cystine
-The same patient may have more than one type of stone concurrently (e.g.. calcium and uric acid).
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3
Q

What is the Epidemiology of Nephrolithiasis?

A
  • Prevalence 2-3% in general population
  • Estimated lifetime risk about 12% for men 5% for women
  • Approximately 50% of patient with previous urinary calculi have recurrence within 10 years.
  • The rate of urolithiasis increases with age, is higher in men compared to women, and caucasians compared to other races
  • It has been estimated that 7-10 of every 1,000 hospital admission are due to stones.
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4
Q

What are the Risk Factors of calcium stones?

A
  • History of prior calcium urolithiasis
  • Family history of urolithiasis
  • Diet
  • Medications
  • Hyperparathyroidism
  • Hypercalcemia of malignancy
  • Sarcoidosis
  • Medullary sponge kidney
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5
Q

What are the Risk Factors of Nephrolithiasis?

A
  • Uric acid lithiasis = radiolucent
  • Struvite stones
  • Cystine stones
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6
Q

Clinical presentation of Nephrolithiasis?

A
  • Renal colic begins suddenly
  • Severe unilateral flank pain– radiating to groin/testicle/labia (T10-S4 dermatome)
  • Pacing, Rocking, Writhing, Constant movement unable to find position of comfort (contrast to peritonitis)
  • Frequently with nausea, vomiting, diaphoresis
  • Tachycardia, Hypertension
  • Gross hematuria and dysuria/frequency/urgency
  • May have CVAT but abdomen is unremarkable
  • Testicles are not tender or swollen
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7
Q

What is the diagnosis of Ureteral colic?

A

-Focused history with RF assessment (family history of calculi, duration and evaluation of symptoms)
-Clinical presentation w/ Physical Exam
-Urinalysis
-CBC
-BMP
-Radiologic tests
(KUB, IVP, US, NCCT scan)

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8
Q

What is an ultrasound?

A
  • Sensitivity19%, specificity 97%
  • Accessible
  • Good for diagnosis of hydronephrosis and renal stones
  • Poor visualization of ureteral stone unless at UPJ or UVJ
  • Detects indirect signs of obstruction: collecting system dilatation (hydroureter), a loss of a ureteric jet
  • Difficulty in measuring the size of a stone
  • Procedure of choice for patients who should avoid radiation, including children, pregnant women and woman in childbearing age.
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9
Q

What is KUB?

A
  • Sensitivity 45-59% Specificity 71-77%
  • Accessible and inexpensive.
  • May be sufficient to document the size and location of radiopaque (59%) urinary calculi ( Ca oxalate, Ca phosphate), but radiolucent stones such as pure Uric acid, pure Cystine, Indinavir, pure matrix
  • Unfortunately stones are frequently obscured by stool or bowel gas, ureteral stones overlying the bony pelvis or transverse processes of vertebrae .
  • Furthermore, non-urologic radio-opacities, such as calcified mesenteric lymph nodes, gallstones, stool and phleboliths may be misinterpreted as stones.
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10
Q

What is Ivp study?

A
  • Sensitivity 64-87% Specificity 92-94%
  • Relatively safe despite the need for contrast (If CT is unavailable)
  • Provides information about the stone (size, location, radiodensity) and degree of obstruction.
  • Serum Cr must be measured before the test
  • Nephrotoxic effect is minimized by adequate hydration, minimum amount of contrast material used.
  • Poor visualization of non-genitourinary structures
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11
Q

What is Noncontrast helical ct?

A
  • Fast, accurate, and readily identifies all stone types in all location (pure matrix stones and Indinavir stones not seen)
  • Sensitivity 95-100% , Specificity 94-96%
  • Expensive
  • CT should not be used as a first line test with pregnant/child/suspicion of gynecologic etiology
  • Findings consistent with calculi on CT
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12
Q

What is >5mm management?

A
  • Open nephrostomy
  • Percutaneous nephrostolithotomy
  • Ureteroscopy
  • Extracorporeal shock wave lithotripsy
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13
Q

What is Staghorn calculi?

A

Upper urinary tract stones involve the renal pelvis and extend into at least 2 calyces

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14
Q

What is the Work up for recurrent stones?

A
  • calcium stones
  • Uric acid
  • Cystine
  • Struvite
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15
Q

What is the Pathology of Bladder cancer?

A

Transitional cell carcinoma

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16
Q

What is the Epidemiology of Bladder cancer?

A
  • 90% >55yo
  • Men have more incidence of bladder cancer than women
  • Cancers are more common in caucasian – 2:1.
17
Q

What is the Risk factors

of Bladder cancer?

A

Occupational exposures**

18
Q

Signs and symptoms of Bladder cancer?

A
  • Painless Hematuria (80-90%)
  • Urinary voiding symptoms(LUTS)(20-30%)
  • Symptoms of advanced disease
19
Q

What is the Work up of Bladder cancer?

A

-Urinalysis
-Cystoscopy
(Diagnostic standard w/ bx)
-CT scan w/ contrast, U/S and/or MRI

20
Q

What is the Tnm staging?

A
  • T1 Tumor in wedge subepithelial connective tissue
  • T2 Tumor in wedge muscle
  • T3: through the muscle layer of the bladder and into surrounding adipose
  • T4: spread beyond the adipose and into nearby organs or structures
21
Q

What is the Prognosis of bladder cancer?

A
  • Overall 10 yr survival is 70%
  • Lesions up to T1, especially TA, have 95% survival rate
  • Muscle invasive carcinoma 5-year survival rates are 70%
  • Regional lymph node involvement 5-year survival rate is 35% and distant mets 5%
22
Q

What is Treatment for bladder cancer?

A

-Muscle invasive versus non-muscle invasive treatment modalities
-Non-muscle invasive disease
-Surgery (Endoscopic TURBT, Radical cystectomy)
-Immunotherapy and chemotherapy
(Intravesicle instillation)

23
Q

What is Renal cell carcinoma?

A
  • the proximal renal tubular epithelium

- 90-95% of all renal cancers

24
Q

What are the Signs and symptoms of Renal cell carcinoma?

A
  • Hematuria
  • CLASSIC TRIAD flank pain, hematuria, flank mass
  • Frequent occurrence w/ paraneoplastic syndromes
25
Q

What’s the diagnosis of of Renal cell carcinoma?

A

-Labs
(Anemia/Erythrocytosis, CMP, Hematuria. Elevated ESR
-Imaging
(Ultrasound, CT w/ contrast. MRI. Bone scan, PET Scan)

26
Q

What is the Rcc staging?

A

-Stage I:—Tumor is confined within the kidney parenchyma (no involvement of perinephric fat, renal vein, or regional lymph nodes).
Ia: <4cm
Ib: 4-7cm
-Stage II:—Tumor (>7cm) involves the perinephric fat but is confined within Gerota’s fascia (including the adrenal).
-Stage IIIA:—Tumor involves the main renal vein or inferior vena cava
-Stage IIIB:—Tumor involves regional lymph nodes
-Stage IIIC:—Tumor involves both local vessels and regional lymph nodes.
-Stage IVA:—Tumor involves adjacent organs other than the adrenal (colon, pancreas, etc).
-Stage IVB:—Distant metastases

27
Q

What’s Rcc prognosis?

A
-Tumor size
(>10cm 0% @5yr, 5-10cm 50%, <5cm 84%)
-Multiple lymph node involvement dire prognostic sign
-Overall stage survival (1 yr vs 5 yr) 
Stage 1 : 91-100% (81%)
Stage 2 : 74-96% (74%)
Stage 3 : 59-70% (53%)
Stage 4 : 16-32%  (8%)
28
Q

Whats Rcc treatment?

A
-Localized disease(w/in kidney)
(T1a <4cm partial nephrectomy,
T1b-T2 radical nephrectomy)
-Locally invasive RCC
-Disseminated Disease
-Locally advanced disease