Neooplastic diseases Flashcards

1
Q

This cancer is most commonly asymptomatic in early stages. It is the second most common cancer in males

A

Prostate Ca

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2
Q

What are the risk factors for prostate ca?

A

1) age
2) AA
3) high fat diet
4) FHx
5) Exposure to pesticides

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3
Q

What symptoms are common in late stage prostate Ca?

A

urethra obstruction, urinary retention, urinary frequency…..mets cause bone pain, wt loss

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4
Q

Although screening for prostate cancer is controversial, what are the current recommendations?

A
Use combination of
1)  PSA
2)  DRE
3)  TRUS
4)  bx
PSA  >10ng/mL = TRUS+bx
\+DRE = TRUS+bx
PSA = 4-10 with neg DRE, discretion
Neg PSA, Neg DRE = annual f/u
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5
Q

What are the tx’s for prostate cancer?

A

Radiation (SEEDS)
prostatectomy
Anti androgens
watchful waiting

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6
Q

The cause of this cancer is unknown, but it accounts for about 85% or primary renal cancers and is twice as common in men.

A

Renal Cell Carcinoma (RCC)

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7
Q

What are risk factors for RCC?

A

***smoking, heavy use of analgesics, polycystic kidney dz, chronic dialysis, heavy metal exposure, htn

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8
Q

How does RCC present?

A

1) hematuria
2) abdominal/flank pain
3) abdominal mass
4) wt loss, fever

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9
Q

How can you definitively dx RCC?

A

CT w/ and w/o to DIAGNOSE and stage. (U/S good for detection of “mass” only)

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10
Q

How do you treat RCC?

A

nephrectomy. (partial nephrectomy for small local tumor). Chemo is not effective

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11
Q

Where does RCC originate?

A

PCT cells

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12
Q

2% of all RCC is hereditary

A

That’s just some fun FYI. They are crazy names like Von Hippel-Lindau syndrome and hereditary leiomyoma-renal cell carcinoma and my fave, the Birt-Hogg-Dube syndrome…..but I doubt we need to go that far.

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13
Q

You have a newly dx’ed RCC patient. What do you expect to see on labs?

A

hematuria (usually), erythrocytosis (increased erythropoietin) OR anemia (decreased erythropoietin, yhpercalcemia

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14
Q

This cancer is most common in men b/t 20-35 years old. It has a high cure rate (95%) compared to other cancers

A

Testicular cancer

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15
Q

Testicular cancer is almost always an abnormal proliferation of the _________cells.

A

Germ cells (I’m pretty sure testicles are full of germs)

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16
Q

Tumors in what 2 cells are typically benign?

A

Leydig cells and Sertoli cells

17
Q

What are the risk factors for testicular cancer?

A

cryptorchidism (even after surgical correction) and Klinefelter’s syndrome

18
Q

What s/s will you look for when screening for testicular cancer?

A

painless mass of the testicle and gynecomastia (sometimes) b/c some germ cells produce gonadotropins

19
Q

How do you make a definitive dx of testicular cancer?

A

Mass on exam–>U/S to localize,check tumor markers (beta-hCG and AFP), AND ORCHIECTOMY

20
Q

How do you treat testicular cancer?

A

Eval testicle s/p orchiectomy. Then stage cancer. This can be done with serial tumor markers to check progress. Also stage by obtaining CT of chest, abd/pelv. Some testicular cancers (seminoma) do well with radiation after orchiectomy. Rarely, chemo is used for cancer when tumor markers do not decrease s/p orchiectomy

21
Q

Where would you expect to find testicular cancer metastases? And what symptoms would be red flags?

A

Retroperitoneal mets (back pain), lungs (cough), vena cava (LE edema)

22
Q

It appears that clinicians MISDIAGNOSE testicular cancer about 25% of the time. So they remove the testicle and find not cancer, but ___________________

A

an epidermoid cyst (totally benign, can be small or large, located under the tunica albuginea)

23
Q

When removing a testicle, should you approach through the scrotum or the inguinal ring? why?

A

Inguinal ring for 2 reasons.

1) Scrotal approach can lead to tumor seeding of the scrotum (BAD)
2) Inguinal approach allows exploration of spermatic chord for advancement of cancer

24
Q

This is one of the most common types of tumor of the GU tract and can occur anywhere from the kidney to the bladder. 90% of the time, this is a transitional cell carcinoma.

A

Bladder cancer

25
Q

Does bladder cancer typically recur after removal?

A

yes

26
Q

What are the risk factors for bladder cancer?

A

male, smoking, industrial carcinogens, the drug cyclophaosphamide

27
Q

what is the first sign of bladder cancer? Any additional symptoms?

A

***hematuria (typically painless), and then some patients will have dysuria or frequency

28
Q

How do you make a diagnosis?

A

1) UA C&S–to r/o infection
2) urine cytology to detect malignant cells
3) cystoscopy + biopsy
4) Stage with CT of chest

29
Q

What is the tx of bladder cancer?

A

Stage 0 - limited to mucosa = transurethral resection +/- chemo
Stage A - lamina propria = same as above
Stage B - muscle invasion = cystectomy, remove prostate/hysterectomy
Stage C - extends to fat = same as above
Stage D - mets = cystectomy + chemo

30
Q

What are common lab findings for patients with bladder cancer?

A

UA = gross hematuria. Azotemia (post-renal failure). Anemia (blood loss or mets to bone marrow). Occasionally a/w UTI

31
Q

What is neat about the chemo for bladder cancer?

A

It can be administered directly to the bladder via the urethra.

32
Q

At what stage is bladder cancer typically detected? What is the prognosis?

A

up to 80% detected in stage 0 or stage 1, prognosis is good with 81% survival at 5 years.

33
Q

___________is a rare kidney cancer that primarily affects children. It is also known as a nephroblastoma.

A

Wilms’ tumor

34
Q

What age is most susceptible to Wilms’ tumor?

A

Ages 2-5 years

35
Q

How does the Wilms’ tumor typically present?

A

asymptomatic abdominal mass/swelling (83%), htn (25%), fever (23%), hematuria (21%)

Also: GU malformation (meaning kids with congenital defects are at higher risk)

36
Q

Your 4 year old patient has a normal CBC, mild anemia, normal BUN/creat, trace blood and leuks on UA. She has a smooth, well demarcated, nontender abdominal mass. What is your diagnosis?

A

Wilms’ tumor (my point is, labs are pretty normal, just trace anemia and UA has trace blood/wbc’s)

37
Q

How do you diagnose a Wilms’ tumor?

A

U/S or CT of abdomen. Stage with CT of chest. (Mets likely in vena cava, lungs, and liver)

38
Q

What is the treatment for Wilms’ tumor?

A

Surgical excision followed by both chemo (5 days s/p sx) and radiation (10 days s/p sx)