Renal Feirstein Flashcards

(38 cards)

1
Q

What is the epidemiology of RCC

A

M>W
avg onset 64 y/o
73% have a 5 year survival

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2
Q

What are the RF for RCC

A

SMOKING

HTN, obesity, chronic dialysis, increased ASA, NSAID, or APAP use, genetics, toxin exposures

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3
Q

What is the pathology of RCC

A

MC* clear cell: 3p deletion
Papillary/chromophilic (type 1 good prog, type 2 aggressive)
Chromophobe (oncocytic)

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4
Q

What is the triad associated with RCC

A

Hematuria
Flank pain
Abdominal mass

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5
Q

What are other symptoms of RCC

A
scrotal varicocele 
weight loss 
ascites 
pulmonary emboli (IVC) 
mets to lungs, lymph, bone, liver, brain
paraneoplastic syndrome
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6
Q

How do you diagnose RCC

A

**abdominal CT w/ wo contrast
but can also use MRI
Tissue biopsy
to eval mets: bone scan, CT chest, MRI w/ contrast, or PET

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7
Q

How do you treat RCC

A

Localized (stage I-III): surgery is curative

Advanced (stage IV): systemic Tx, surgery, and radiation

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8
Q

What is a “small renal mass”

A

<4cm and enhances on contrast imaging
<2cm: usually benign (10% RCC)
4+cm: small% benign, 20-30% RCC

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9
Q

What are predictors of malignancy in a small renal mass

A

Male

increasing tumor size

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10
Q

What can be used to diagnose small renal masses

A
renal CT/MRI w/wo
CMp
CBC
renal function tests 
chest imaging (mets?) 
\+/- biopsy 
**involve urology!
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11
Q

How do you manage a small renal mass

A

surgery!
<3cm: thermal ablation w/ biopsy
<2cm: imaging q 3-6 months for 2 yrs, then q 6-12 months
<1cm: surveillance

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12
Q

What is the MC primary pediatric renal tumor

A
Wilms Tumor (<15 y/o) 
-abnormal renal development and loss of tumor suppressor gene function
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13
Q

What does Wilms look like

A

Solitary
surrounded by enhancing pseudocapsule
made of blastemal, stromal, and epithelial cells

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14
Q

Wilms tumor usually presents with

A

Abdominal mass, otherwise asymptomatic

rarely: abd pain, fever, HTN, hematuria

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15
Q

What is needed to definitively diagnose Wilms tumor

A

Biopsy (need histologic confirmation)
but, start w/ US, then CT or MRI before invasive biopsy
**check the other kidney!!

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16
Q

Labs done for Wilms tumor include

A

renal and liver function tests
UA, calcium, CBC, coags
refer to peds and get chest imaging for mets

17
Q

Why check coags in Wilms tumor

A

because many have associated Von Willebrand factor bleeding disorder

18
Q

What is the outcome of Wilms tumor

A

90% 5 year survival rate with chemo and surgical excision

BUT, increased risk for premature death as adult d/t chemo and radiation

19
Q

What should we do for surveillance in Wilms tumor patients

A

CXR, abd US, CT
q 6-8 weeks during treatment
q3 months for 2 years
q 6 months for 2 years after that

20
Q

What is renal vascular disease

A

a cause of secondary HTN (due to atherosclerotic disease* or fibromuscular dysplasia) associated with target organ injury (LVH, renal fibrosis)

21
Q

What are important Ddx for renal vascular disease

A

thromboembolic renal disease (in old and hypercoagulable, w/ flank pain, leukocytosis, n/v, HTN, renal decline)
Microvascular injury 2/2 HTN (hypertensive nephrosclerosis, arteriolonephrosclerosis)

22
Q

When should you consider renal vascular disease as a diagnosis

A
Young onset, severe/resistant HTN, acute rise in BP 
SrCr increase >30% s/p ACE/ARB 
mod-severe HTN w/ flash pulm edema 
New onset Stage II HTN >55 y/o 
abdominal bruits
23
Q

What do renal vascular disease labs show

A

increased BUN/Cr

24
Q

How do you diagnose renal vascular disease

A

**renal arteriograph
also doppler, CTA
MRA last resort d/t complications with gandolinium

25
When do you order diagnostic testing
only if intervention will be completed!
26
What is atherosclerotic RAS
atherosclerosis leading to decreased renal blood flow involving the aorta or proximal main renal artery - it is a cardiac risk equivalent! - onset usually >45 y/o
27
What are RF for atherosclerotis RAS
HLD smoking 50+ y/o comorbid CAD/PAD
28
How do you diagnose atherosclerotic renal artery stenosis
60-75% luminal occlusion
29
How do you treat ARAS
treat HTn monitor CKD secondary prevention (STATINS! ASA, stop smoking)
30
What is fibromuscular dysplasia
non-inflammatory, non-atherosclerotic disorder leading to arterial stenosis, occlusion, aneurysm, dissection, or tortuosity AKA decreased renal blood flow
31
What does FMD involve
distal main renal artery (unlike atherosclerotic which involves proximal) or intrarenal branches
32
What does FMD show on angiography
multifocal (string of beads) vs focal (circumferential stenosis)
33
What is the clinical presentation of FMD
``` HA pulsatile tinnitus neck pain flank/abd pain HTN TIA bruits ```
34
How do you treat FMD
ACE/ARB (need SrCr q6 mo, and duplex q6-12 mo) | *Angioplasty (need duplex and SrCr @ 1st post-op, q6 mo for 2 years, then every year)
35
Why are ACE/ARB contraindicated in RAS
normally, stenosis decreases renal perfusion and autoregulation (mediated by angiotensin II) maintains GFR If you block angiotensin II, you stop autoregulation and decrease GFR= AKI BUT, stenosis is what causes renal vascular disease (stenosis) SO be cautious, but ACE/ARB are 1st line for RAS
36
What must you monitor in RAS patient on ACE/ARB
SrCr, to ensure it doesnt rise above 30%
37
What are complications of renovascular disease
renal artery dissection hemorrhage (capsular perforation) atheroembolic disease leading to HTN and kidney failure
38
Who most likely benefits from surgery
Short duration of BP prior to diagnosis meds dont control BP (intolerant to meds) recurrent flash pulmonary edema/HF