Renal Tumors And Congenital Anomalies Flashcards

1
Q

Renal Tumors
- Malignant:

A

• 85% Adenocarcinoma.
• 15% Wilms, TCC, sarcomas.

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2
Q

Renal Tumors Benign

A

Oncocytoma, angiomyolipoma.

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3
Q

Renal Cell Carcinoma “RCC”

A
  • Most lethal urological cancer.
  • 5th most lethal cancer.
  • Adenocarcinoma from the renal cortex.
  • Arises mostly from proximal tubule.
  • More common in males.
  • In 50-60s.
  • Unilateral, solitary, solid.
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4
Q

Renal Cell Carcinoma “RCC” RFs

A

• Smoking: ×2.3.
• Renal failure with cysts: ×30.
• Obesity, HTN.
• Polycystic kidney disease.
• Sickle cell.

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5
Q

RCC Histological types:

A

• Clear cell: MC.
→ Proximal tubule, very vascular, VHL gene on Ch 3.
• Papillary: bilateral, Ch 7, 17.
• Chromophobe: cortical part of collecting, least aggressive.
• Collecting duct: young, poor prognosis, rare.
• Medullary: sickle cell, young and aggressive

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6
Q

RCC genetics

A

VHL syndrome:
Sporadic RCC associated in 80% with VHL mutation.
Papillary RCC: AD, CH 7 C-met activation.

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7
Q

VHL syndrome:

A

→ Autosomal Dominant.
→ Mutation in VHL gene in chromosome 3.
→ Associated with: bilateral RCC, hemangioblastoma,
polycythemia.

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8
Q

RCC Presentation:

A

• Mostly incidental.
• Painless hematuria: 60%, MC.
• Loin pain: 40%.
• Mets symptoms: 30%.
• Para-neoplastic syndrome: 30%.
→ Hypercalcemia, polycythemia, fever, hypertension, hepatic dysfunction, hypoglycemia.

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9
Q

RCC Investigations:
• Labs:

A

→ CBC, ESR.
→ KFT.
→ LFT.
→ Urine analysis & culture.

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10
Q

RCC Images:

A

→ Renal protocol enhanced CT: GOLD STANDARD.
→ Chest CT for staging.
→ Bone scan: if symptomatic.

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11
Q

RCC Spread:

A

• Renal Vein 44%.
• Bone 25%.
• Hematogenous: lung (MC). bone, liver, brain.
→ Paired organs metastasize to lung more.
→ Single organs metastasize to liver more.
• Lymphatic.

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12
Q

RCC Treatment:

A

• Radical nephrectomy or partial nephrectomy (nephron
sparing surgery).
• Chemotherapy usually has no role.
• Radiotherapy: palliation in metastatic patients.

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13
Q

Wilms Tumor “Nephroblastoma”

A
  • The MC renal cancer in childhood.
  • Usually bilateral.
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14
Q

Wilms Tumor “Nephroblastoma” DDx

A

Neuroblastoma, Hydronephrosis.

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15
Q

Wilms Tumor “Nephroblastoma” Investigations

A

• Tests:
→ Bone marrow biopsy.
→ Urine collection for VMA & metanephrines.
• Images:
→ IVU, MRI.

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16
Q

Wilms Tumor “Nephroblastoma” Tx:

A

nephrectomy -/+ chemoradioimmunotherapy.

17
Q

Oncocytoma

A
  • Central scar: spoke wheel appearance.
  • Looks like chromophobe RCC in histology.
  • Biopsy is not diagnostic in most cases
  • Tx: Nephrectomy.
18
Q

Angiomyolipoma

A
  • Females more than males.
  • Associated with tuberous sclerosis(AD).
  • Histology: very vascular and contains fat.
  • Presentation: incidental vs bleeding.
  • Tx: if symptomatic→ surgery, angioembolization.
  • Can be differentiated from renal cell carcinoma by contrast CT.
19
Q

Hypospadias

A

• Urethra opens in an abnormal position on the ventral
aspect of the penis.
• Associated with chordee and hooded prepuce

20
Q

Vesico-ureteral reflux (VUR):

A

• Child with HTN and recurrent UTI.
• Urographic demonstration of longitudinal folds in renal
pelvis and ureter in children.

21
Q

MC cancer in renal transplant patients:

A

skin cancer (BCC).

22
Q

Renal transplantation is usually defined as a

A

heterotopic graft.

23
Q

MC site of ureteral urothelial tumor:

A

bladder and pelviuretric

24
Q

Horseshoe kidneys:

A

• The MC fusion anomaly.
• More in males.
• True fusion of the lower poles at the level of L4 or L5
→ Which forms an isthmus and becomes medially directed.
• High incidence of neoplasia.

25
Q

Ectopic ureter

A

A ureter that opens some location other than the bladder.

26
Q

Ectopic ureter: MC sites in males:

A

Posterior urethra and seminal vesicles

27
Q

Ectopic ureter: MC sites in females:

A

Urethra, vestibula and vagina.