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MJ- F2 E5- Renal > Renal Tumors- MJ > Flashcards

Renal Tumors- MJ Flashcards

1
Q

Which renal carcinoma?

  • Most common in men
  • Median age of dx= 64y/o (6th-8th decades)
  • Strong association w/ smoking
A

Renal Cell Carcinoma

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2
Q

Which is the MC primary renal malignancy?

A

Renal Cell Carcinoma

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3
Q

What is the biggest risk factor for Renal Cell Carcinoma?

A

SMOKING

(will be on exam)

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4
Q

The following are risk factors for which renal tumor?

  • Smoking
  • HTN
  • obesity
  • chronic dialysis
  • toxic exposure (abestosis)
  • Heavy ASA, NSAIDs or Acetaminophen use
  • Genetics
A

Renal Cell Carcinoma

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5
Q

What is the most common type of renal cell carcinoma?

A

Clear Cell (75-85%)

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6
Q

Which type of renal cell carcinoma?

  • Depletion of Chromosome 3p
  • Proximal tubule
  • usually solid
A

Clear Cell Renal Cell Carcinoma (the MC)

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7
Q

Which type of Renal Cell Carcinoma?

  • Less common (10-15%)
  • Proximal Tubule
  • Type 1- usually stage I or II at dx, good prognosis
  • Type 2- aggressive, usually stage III or IV at dx
A

Papillary (chromophilic) Renal Cell Carcinoma

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8
Q

What is the classic presentation of Renal Cell Carcinoma (3 things)

A
  1. Hematuria (MC)
  2. Abdominal Mass
  3. Flank pain
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9
Q

The following are the clinical presentation of what?

  • Hematuria
  • abdominal mass
  • flank pain
  • Weight loss
  • L-sided scrotal varicocele

(bolded= MC)

A

Renal Cell Carcinoma

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10
Q

What are the 5 MC site of metastasis for Renal Cell Carcinoma?

A
  1. Lungs
  2. Lymph Nodes
  3. Bone
  4. Liver
  5. Brain
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11
Q

The following paraneoplastic syndromes are associated with which renal cancer?

  1. Anemia
  2. Hepatic dysfunction
  3. Fever
  4. Hypercalcemia
  5. Cachexia
  6. Erythrocytosis
  7. Secondary amyloidosis
  8. Thrombocytosis
  9. Polymyalgia rheumatica
A

Renal Cell Carcinoma

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12
Q

What is the initial diagnostic test for Renal Cell Carcinoma?

A

Abdominal CT with/without contras

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13
Q

If you have a patient that you think might have Renal Cell Carcinoma and the initial CT is non-diagnostic (or the patient has a contraindication to contrast), what would be your next choice of test?

A

MRI

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14
Q

What is the definitive diagnostic test for Renal Cell Carinoma?

A

Tissue Biopsy (Nephrectomy or partial nephrectomy)

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15
Q
A
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16
Q

What are the 4 diagnostic tests you should do in order to evaluate for metastasis of Renal Cell Carcinoma?

A
  1. Bone scan (if pain or elevated alk phos)
  2. CT chest
  3. MRI w/ gad (for IVC and R atrium)
  4. PET or PET/CT
17
Q

Other than hematuria, abdominal mass and flank pain, what 4 other sxs might be present in a patient with Renal Cell Carcinoma if there is IVC involvement?

A
  1. LE edema
  2. Ascites
  3. Hepatic dysfunction
  4. Pulmonary emboli
18
Q

What is the treatment for a localized RCC (Stages I, II, III)?

A

Surgery is curative

19
Q

What are the treatment options (3) for advanced RCC (Stages IV)?

A

Options:

  1. Systemic therapy (Immunotherapy, molecularly targeted agents)
  2. Surgery
  3. Radiation

*treatment decisions are dependent on prognosis*

20
Q

What are the predictors of malignancy for a small renal mass, <4cm (w/ enhancement on contrast imaging, solid or complex cyst)?

A

Male sex

Increasing tumor size

21
Q

How do you manage a renal mass that is <2cm?

  • 20-40% are _____
  • 10% high grade ____
  • <1% develop ______
A
  • 20-40% are benign
  • 10% are high grade RCC
  • <1% develop mets
    *
22
Q

Management of small renal mass:

What are the chances of a renal mass that is >4cm being benign? Being high grade or advanced RCC?

A

Increased chance of malignancy!

5-10% benign

20-30% high grade or advanced RCC

23
Q

The following are steps in management of what?

  1. Urology
  2. Dedicated Renal CT or MRI, without and then with IV contrast
  3. CMP and CBC (paraneoplastic syndrome)
  4. Renal function to eval for CKD
  5. Chest imaging if malignancy risk high and concern for Mets
  6. Biopsy decision
A

Management of small renal mass

24
Q

What are the 4 management strategies of small renal masses and at what size are each indicated?

A
  1. Surgery (partial nephrectomy)
  2. Thermal ablation (if < 3cm)
  3. Surveillance (only if <2cm)
  4. <1cm =surveillance (NO biopsy)
25
Q

If you find a small renal mass < 2cm, how would you manage this?

A

Surveillance

Mets eval q3-6mo x2 years then q6-12 month

26
Q

What is the management for a renal cell mass <1cm?

A

Surveillance

(NO biopsy)

27
Q

Which renal tumor?

  • MC primary renal cancer in children < 15 y/o
  • 2/3 dx before 5y/o, 95% before 10y/o
  • Sporadic (NOT genetic)
A

Wilms Tumor

28
Q

Pathology of which Renal Tumor?

•Abnormal renal development

  • Association with loss of function of tumor suppressor genes
  • solitary lesion
  • Surrounded by pseudocapsule
A

Wilms Tumor

29
Q

What is the most common clinical presentation of a wilms tumor?

A

Abdominal mass

(usually an incidental finding by a parent)

30
Q

Other than an abdominal mass, what are 4 other less common presentations for a Wilms tumor?

A
  1. Abdominal Pain
  2. Hematuria
  3. Fever
  4. Hypertension

(“Freddy Had A Hamburger”)

31
Q

What is the definitive diagnosis for a Wilms tumor?

A

Histologic confirmation (surgical excision or biopsy)

32
Q

What is the initial diagnostic study for a Wilms Tumor?

What other test(s) do you perform if you don’t find anything on the initial study?

A
  • Initial study= Abdominal ultrasound
  • If you dont find anything on u/s, you MUST order: CT or MRI w/ contrast
33
Q

T/F: In a patient with a Wilms tumor, you do NOT need to evaluate the contralateral kidney

A

FALSE

It is important to evaluate the contralateral kidney

34
Q

The Following diagnostic labs would be ordered for which renal tumor?

  • renal function
  • U/A
  • liver function
  • calcium
  • CBC
  • coag studies
A

Wilms tumor

35
Q

What is the treatment for a Wilms tumor? (3 steps)

A
  1. Refer to pediatric cancer center
  2. Chest imaging for Mets
  3. Chemo and surgical excision
36
Q

What is the prognosis of a Wilms tumor?

A
  • 5-year survival 90%
  • Increased risk of premature death in adulthood due to secondary neoplasms and other late complications
37
Q

What is a patient with history of Wilms tumor at increased risk of?

A

•Increased risk of premature death in adulthood due to secondary neoplasms and other late complications (i.e. infertility)

38
Q

Surveillance for Wilms tumor after surgical excision and chemo includes what 3 diagnostic studies performed how often?

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

MJ- F2 E5- Renal (13 decks)

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