Renal Carcinoma Flashcards

1
Q

What is the MC primary renal malignancy?

A

RCC

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2
Q

Epidemiology of RCC?

A

M > W

6-8th decades

73% 5 yr survival

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3
Q

What are some risk factors for RCC

A

SMOKING

others: HTN
Obesity
Chronic dialysis 
Toxic exposures
Heavy aspirin, NSAIDS, or acetaminophen use
Genetics
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4
Q

Path of RCC?

A

MC: clear cell- deletion of chromosome 3p, proximal tubule

papillary: proximal tubule

Less common:

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5
Q

Classic triad for presentation of RCC?

A

usually asxs until late disease

HEMATURIA

ABDOMINAL PAIN

FLANK PAIN

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6
Q

Other S/S of RCC?

A

Weight loss

Scrotal varicocele (left-sided)

IVC involvement: lower extremity edema, ascites, hepatic dysfunction, pulmonary emboli

Metastasis: common sites are lungs, lymph nodes, bone, liver, brain

Paraneoplastic syndromes:

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7
Q

Work up for RCC?

A

Abdominal CT w/wout contrast***

MRI

tissue bx - for ANY solid renal mass

To eval for mets: bone scan, CT chest, MRI, PET

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8
Q

Tx for RCC?

A

localized > resection

Advanced: options

  • systemic therapy
  • surg
  • radiation
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9
Q

What are some predictors of malignancy for small renal mass?

A

male sex

increasing tumor, greater than 4cm is higher risk, less than 2 cm more likely to be benign

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10
Q

Management of small renal mass?

A

consult nephrology

dedicated renal CT/MRI

if s/s of paraneoplastic syndrome- CMP/CBC

renal func.

+/- chest imaging

+/- biopsy

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11
Q

Management options for small renal mass?

A

surg

thermal ablation if <3cm

surveillance if <2cm (every 3-6 mo 1st yr, then every 6-12 mos)

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12
Q

Epidemiology of wilms tumor?

A

makes up small number of renal tumors but makes up 95% of renal malignancies in KIDS!

2/3 dx under 5, 95% before 10

sporadic

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13
Q

Path of wilms tumor

A

abn. renal development
assoc. with loss of func. of tumor suppressor genes

usually solitary lesion surrounded by pseduocapsule

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14
Q

Clinical presentation of wilms tumor?

A

ABDOMINAL MASS
-usually smooth and nontender and doesn’t midline

less common: abd pain, hematuria, fever, HTN

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15
Q

Work up for wilms tumor?

A

Definitive: histologic (excision or biopsy)

initial study: Abd US

others: CT/MRI with contrast

Labs: renal func., UA, liver function, Ca, CBC, coag studies

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16
Q

Tx for wilms tumor?

A

refer to peds CA center

Chest imaging to r/o mets

chemo/surg

17
Q

Px for wilms tumor?

A

5 yr survival 90%

but increased risk of premature death in adulthood due to secondary neoplasms and other late comp.

18
Q

Surveillance after tx of wilms tumor?

A

Includes CXR, abd u/s, chest/abd/pelvic CT

Q 6-8 weeks during therapy, q 3 months x 2 years, q 6 months x 2 years

19
Q

What 2 things cause renovascular disease?

A

renal artery stenosis

fibromuscular dysplasia

20
Q

Renovascular disease can be a cause of…

it is assoc. with…

A

secondary HTN

accelerated target organ injury: LVH, renal fibrosis

21
Q

When should we consider renovascular disease as cause for secondary HTN?

A

younger

severe or resistant

acute rise over stable value

22
Q

What else can be seen in renovascular disease?

A

Sr Cr rises >30% after ACE or ARB

mod severe HTN in pt with recurrent episodes of flash pulmonary edema

stage II HTN onset after age 55

mod/severe HTN in pt who have artherosclerosis or small kidney

abd bruit

23
Q

Work up for renovascular disease?

A

Labs: may have BUN/Cr

Gold standard: Renal arteriography- looks for signs of fibromuscular dysplasia

Duplex Doppler US- but not always done (tech error, takes long)

CTA- usually start with this!!

MRA

24
Q

Describe Atherosclerotic renal artery stenosis, etiology?

A

aka ischemic nerphropathy

usually > 45y/o

reduced blood flow to kidney; usually involves aortic orifice or proximal main renal artery

25
Q

RF for atherosclerotic renal artery stenosis?

A

Hyperlipidemia
Cigarette smoking
Age > 50 y/o

26
Q

atherosclerotic renal artery stenosis is a….

A

cardiac risk equivalent

-so start on Statin

27
Q

Dx of atherosclerotic renal artery stenosis

A

luminal occulsion of at least 60-70%

28
Q

Tx for atherosclerotic renal artery stenosis

A

Tx the HTN; monitor CKD; CV secondary prevention; revascularization (angioplasty w/ or w/o stenting or bypass)

29
Q

Who usually gets fibromuscular dysplasia

A

younger women, Less than 50 y/o

30
Q

Etiology of fibromuscular dysplasia?

A

noninflammatory, nonatherosclerotic disorder leading to arterial stenosis, occlusion, aneurysm, dissection, and arterial tortuosity – can effect nearly every arterial bed

31
Q

What can you see on angiography with fibromuscular dysplasia?

A

multifocal (string of beads) vs. focal (circumferential or tubular stenosis)

32
Q

Clinical presentation of fibromuscular dysplasia?

A

H/a, pulsatile tinnitus, neck pain, flank or abdominal pain

HTN, cervical or abdominal bruit, TIA, stroke

33
Q

Management of fibromuscular dysplasia?

A

ACE or ARB, f/o with serum Cr

Surg: angioplasty

34
Q

How do ace/arbs work in renovascular disease?

A

renal perfusion is decreased due to the stenosis

so,

Medical blockade of angiotensin II formation blunts the effect of autoregulation > reduced GFR > possible AKI (hemodynamically induced)

35
Q

Comps of surg. for renovascular disease?

A

Renal artery dissection
Capsular perforation
Hemorrhage
Atheroembolic disease – accelerates HTN and kidney failure

36
Q

Who is most likely to benefit for surg. tx for renovascular disease?

A

Short duration of BP elevation prior to dx

Failure of med therapy to control BP

Intolerance to med therapy

Recurrent flash pulmonary edema and/or refractory heart failure