L15- Renal and Bladder Tumors Flashcards

1
Q

list the common benign renal tumors

A
  • renal adenoma
  • renal oncocytoma
  • angiomyolipoma
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2
Q

list the common malignant renal tumors

A
  • renal cell carcinoma (90%, RCCa)
  • urothelial carcinoma (TCCa)

-Wilm’s Tumor / Nephroblastoma (in children)

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3
Q

Angiomyolipoma is a (benign/malignant) tumor and is considered triphasic because it (2). 50% present with (3) which is usually (4). Some present sporadically and occur with (5).

A
(most common benign tumor)
1- benign (rarely malignant)
2- involves muscle, fat, vessels
3- tuberous sclerosis (25 yrs)
4- asymptomatic, small in size
5- (45 yrs) flank pain, mass, hematuria, retroperitoneal hemorrhage
(good prognosis, treat by excision)
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4
Q

The most common kidney cancer is (1) and it is a (benign/malignant) tumor of the (3). The majority of tumors are described as (single/multiple), (uni/bi)-lateral, (predictable/sporadic).

A

1- RCCa (renal cell carcinoma- 90%)
2- malignant
3- tubular epithelial cells
4- single, unilateral, and sporadic (majority, some are syndrome related)

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5
Q

(1)% of RCCa is hereditary with the following 3 types: (2)

A
1- 5%
2-
i) Autosomal Dominant RCCa
ii) Von-Hippel-Lindau disease (VHL)
iii) hereditary papillary RCCa (multiple and bilateral found in younger people)

glial cell RCCa are most common

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6
Q

RCCa mostly in occurs in (1) age group among (males/females) most.

A

1- 50s

2- males > females (2:1)

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7
Q

RCCa usually presents with (1) as the most common sign with (2) as a very seldom accompanied sign. One of the most distinguishing features is that RCCa causes (3).

A

1- hematuria
2- flank pain, (palpable mass <10% of Pts)
3- paraneoplastic syndrome

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8
Q

describe the related issues of RCCa and paraneoplastic syndrome

A
  • polycythemia (EPO)
  • HTN (renin)
  • hypercalcemia (PTH)
  • Cushing’s syndrome (ACTH)
  • leukemoid rxn (leukoxytosis)
  • amyloidosis
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9
Q

RCCa is diagnosed via….

A
  • renal US
  • CT
  • IV pyelography
  • biopsy
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10
Q

RCCa is graded based on (1).

Describe the 4 stages of RCCa: (2)

A

1- nucleus appearance: Fuhrman 1-4

2-
Stage I) confined to kidney (5yrs, 60-80%)
II) perirenal fat (5yrs, 40-70%)
III) lymph node + IVC (5yrs, 10-40%)
IV) adjacent organs / metastasis (5yrs, 5%)

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11
Q

RCCa is treated by….

A

nephrectomy (radical or partial)

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12
Q

(1) is the most common solid tumor in children, usually affecting them before (2) y/o. It is the result of a (3) mutation.

A

1- Wilm’s Tumor
2- <6 y/o (90%)
3- 2 mutated suppressor genes (WT1/WT2 loss of function mutations; *somatic mutation, not inherited)

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13
Q

Wilm’s tumor appears (1) on gross inspection. It is considered to have a triphasic pattern because (2). (3) is the main description of cell status upon microscopic investigation.

A

1- single, well circumscribed, encapsulated, soft, fleshy, grey-white/tan
2- it involves blastema, stroma, epithelial (tubular structure and glomeruli)
3- anaplasia (nuclear size is 3x bigger, abnormal mitosis)

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14
Q

list and briefly describe the 3 congenital abnormalities involved with the bladder (malformations)

A
  • Extrophy: bladder protrudes out of abdomen wall
  • Diverticula: extra pouch stemming from bladder wall (through the muscle, inc chance for infection, renal stones)
  • Urachus: remnant of allantois which drained fetal bladder via umbilical cord (urine from navel and cyst in canal is common)
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15
Q

list the 3 inflammatory (infectious) lesions of the bladder

A
  • acute cystitis
  • chronic interstitial cystitis
  • malacoplakia
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16
Q

Cystitis (acute) is more common in (males/females) because of (2).

A

1- females

2- short urethra

17
Q

list the common pre-disposing factors that help lead to cystitis (acute)

A

(females > males, short urethra)

  • DM
  • instrumentation (catheter, cystoscopy)
  • bladder calculi (stones)
  • bladder outlet obstruction (BPH)
18
Q

Cystitis (acute) is usually secondary to (1), but it can also occur as a result of (2).

A

1- Infection:

  • bacteria: E.Coli, Proteus, Klebsiella, Enterobacter
  • fungus: Candida
  • parasite: Schistoma hematobium

2- Iatrogenic: chemotherapy, radiation => hemorrhagic cystitis

19
Q

list the symptoms / clinical presentation of cystitis (acute)

A
  • urinary frequency (up to 20 times daily)
  • dysuria (pain or burning micturition)
  • microhematuria
  • pain over bladder / suprapubic pain
  • fever, chills

(Dx via UA)

20
Q

Chronic interstitial cystitis is caused by (1) and is most common in (2) people (age/gender).

A

1- unknown

2- middle aged women

21
Q

list the signs and symptoms of chronic interstitial cystitis

A
  • suprapubic pain (pain with bladder filling)
  • urinary frequency / urgency
  • nocturia, hematuria
22
Q

Chronic interstitial cystitis has (1) appearance on cystoscopy and (2) via pathological examination

A

1- edema, hemorrhage, ulceration

2- chronic inflammation, mast cells

23
Q

list the 3 types of urothelial neoplasms (indicate if usually benign or malignant)

A
  • Epithelial
  • Mesenchymal (sarcomas, bengin or malignant, not kidney)
  • secondary tumors (metastatic tumors via kidney, not common)
24
Q

list the breakdown of epithelial tumors

A

Benign: urothelial papilloma

Malignant: urothelial carcinoma (TCCa, 90%), SCC (via infection, 7%), adenocarcinoma (via Urachus, 1-2%)

25
Q

describe the 4 types of gross features of urothelial tumors (aka the 4 classifications)

A

i) Papilloma (papillary carcinoma)
ii) Invasive papillary carcinoma

iii) flat noninvasive carcinoma (carcinoma in situ, serious dysplasia)
iv) flat invasive carcinoma

26
Q

Urothelial carcinomas, aka (1), are most common in (2) age group and more common in (males/females). It is also associated with the following mutations: (4).

A

1- TCCa (transitional cell carcinoma)
2- 50-80 y/o
3- males > females, 3:1
4- p53, Rb, p16 genes

27
Q

list the risk factors for bladder cancer

A
  • Smoking: biggest factor, inc 2x
  • Drugs: analgesic abuse (phenacetin), cyclophosphamide
  • Chemicals (in workplace): naphthylamine, rubber
  • Infections: schistosomiasis (parasite)
28
Q

list the clinical features of urothelial carcinoma

A
  • painless hematuria (70-90%)
  • dysuria (20%)
  • urinary urgency / frequency
  • flank pain
  • metastatic disease (up to 20%)
29
Q

(1) is the most common bladder tumor. It grows (endo/exo)-phytic and is a (high/low) grade tumor with (superficial/deep) invasion, (no/single/multiple) recurrences, and is describes as (uni/multi)-focal in terms of the urinary tract.

A

1- Papillary carcinoma (75%)

exophytic, both low/high grade, superficial invasion, multiple recurrences, multifocal (multiple locations on urinary tract)

30
Q

flat noninvasive urothelial carcinoma is also called…

A

carcinoma in situ (CIS)

31
Q

Most invasive urothelial carcinomas are (flat/papillary) and are (high/low) grade tumors with frequent metastasis to (3), therefore giving it a (good/poor) prognosis.

A

1- flat (papillary is ~10% of invasives)
2- high grade (poor differentiation)
3- regional nodes, liver, lung, bone
4- poor prognosis

32
Q

describe the treatment for urothelial carcinomas based on stage

A

i) CIS: TUR (transurethral ressection) if localized, chemotherapy if multifocal
ii) noninvasive papillary: TUR
iii) invasive CA: TUR if superficial, surgical/cystectomy if deep, radiotherapy
iv) metastatic CA: chemotherapy

33
Q

list the prognostic factors affecting Stage and Grade of urothelial carcinomas

A

Stage: depth of invasion of bladder wall, nodal metastases, distant metastases

Grade (via architecture and cytology): low and high grade

34
Q

The 5 yr survival rate for urothelial carcinomas is (1).

  • (2) for 10 yr rate in low grade tumors
  • (3) for 10 yr rate in high grade tumors
  • (4) for 5 yr rate in deeply invasive tumors
A

1- 57%
2- 98%
3- 40%
4- 20%

35
Q

SCC urothelial neoplasm is a (primary/secondary) tumor, mostly caused by (2) and has a (good/bad) prognosis

A

1- primary (5% of total)
2- Schistosoma Hematobium (parasite)
3- bad, the worst prognosis