Renal Neoplasia + Urinary Tract Cancer Flashcards

0
Q

What is renal cell carcinoma?

What does it present as?

A

Malignant epithelial tumour from PCT

PALPABLE PASS, flank pain, haematuria

Paraneoplastic's =
Renin = hypertension
ACTH = cushions
PTH RPA = hypercalcaemia
EPO = polycythaemia
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1
Q

Patient has tuberous sclerosis what kidney tumour does this patient have ?
What exactly does this consist of?

A

Angiomyolipoma = hamartoma of

blood vessels, smooth-muscle, adipose

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2
Q

Explain why in renal cell carcinoma patient rarely presents with right-sided varicocoel?

A

Left spermatic vein trains into the left renal vein hence why you get right varicocoel

Right spermatic vein drains into the IVC directly – > right RCC wouldn’t affect drainage of Right.spermatic vein

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3
Q

Why do we see On gross examination and microscopic examination of renal cell carcinoma

A

Gross exam = reveal yellow mass
Microscopic exam = clear cytoplasm
Hence RCC = clear cell type

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4
Q

What are the two types of renal cell carcinoma

A

Sporadic =
single tumour @upper lobe of kidney @adult=smoker

Hereditary = von Hippel-Lindau syndrome = AD
Multiple + bilateral tumour in kidney + young

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5
Q

Loss of what gene causes renal cell cancer?

What is the staging of renal cell cancer?

A

Loss of VHL tumour suppressor gene – >

increased IGF 1 =
promote growth
+
⬆️ HIF transcription factor = ⬆️ VEGF + ⬆️ PDGF

T = tumour size + renal vein involvement = haematogenous spread to lungs+bones

N = spread to retroperitoneal LN

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6
Q

What is the most common primary renal malignancy?

Treatment of RCC?

A

Renal cell carcinoma

Reception, immunotherapy

Chemo and radiation = shit

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7
Q

At 2 - 4-year-old child presents with a renal malignancy?

A

Wilms’ tumour Nephroblastoma

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8
Q

What does a Wilms’ tumour consist of ?

A

Blastema which is primitive tissue from which kidney forms – >
produces primitive glomeruli+tubules & stromal cells

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9
Q

Patient presents with Wilms’ tumour aniridia congenital abnormality and mental and motor retardation
what syndrome does he have?
what gene issue is this related to ?

A

WAGR syndrome

W T1 tumour suppressor gene deletion

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10
Q

Patient presents with Wilms’ tumour progressive renal glomerular disease and pseudohermaphroditism

What gene issue does he have?

A

W T1 tumour suppressor gene mutation

Denys-Drash syndrome

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11
Q
Patient presents 
wilms tumour 
hemihypertrophy on one side of the body,
organomegaly @ tongue (macroglossia,
Neonatal HYPOglycaemia

What gene issue does he have

A

WT2 tumour suppressor mutation

Beckwith Weidemann syndrome and

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12
Q

What is the most common type of lower urinary tract cancer?
Where does this tumour arise from?

What is the most common location of the lower urinary tract?

A

Urothelial/transitional cell carcinoma

Malignant tumour arising from urothelial lining of
– Renal pelvis
– Ureter
– Bladder = most common location!!!!
– Urethra
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13
Q

What are the risk factors for urothelial transitional cell carcinoma?

A

Pee SAC

  • Phenacetin
  • Smoking – polycyclic aromatic hydrocarbons + naphthylamine
  • Aniline/Azo dyes
  • Cyclophosphamide
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14
Q

An adult presents with painless haematuria with no casts. What does he have?

A

Urothelial/Transitional cell carcinoma

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15
Q

Who was in the two types Of urothelial/transitional cell carcinoma

A

Papillary pathway = tumour develops as papillary growth

Papilla = fibrovascular call with blood vessel running through it. Low-grade – >highgrade – >invade

Flat pathway = P 53 mutations – >
Start as Highgrade – >invade

16
Q

Why do patients with urothelial transitional cell carcinoma presented multifocal tumours with recurrence?

A

Carcinogens hits bladder urothelium over long period of time – >
whole field = mutated – >
multifocal tumours + many mutations = Field defect

17
Q

Middle Eastern Male comes in with painless haematuria. What does he have ?

A

Schistosoma haematobium – >

squamous cell carcinoma of bladder

18
Q

Explain the pathogenesis of squamous cell carcinoma of the bladder

A

Schistosoma haematobium, Smoking,
Chronic cystitis/nephrolithiasis – >

Chronic irritation of bladder – >
squamous metaplasia – > Dysplasia – >
squamous cell carcinoma – >painless haematuria

19
Q

What is adenocarcinoma of the bladder

A

Malignant of proliferation of glands at the bladder

20
Q

Does the bladder have squamous or glandular epithelium?

A

No

21
Q

What is the urachus remnant?

what is it lined by?

A

The urachus is a duct that connects the fetal bladder to the yolk Sac to allow waste drainage into the yolk sac

Extends from the dome of the bladder through the umbilical cord

Lined by glandular epithelium

22
Q

What are the three reasons why a patient can develop adenocarcinoma of the bladder?

A

failure to Involute urachus – > remnant left = lined by glandular epithelium – >
adenocarcinoma @ dome of bladder

Cystitis glandularis – >chronic bladder inflammation
– > metaplasia – > adenocarcinoma

congenital failure to fall CAUDAL portion of anterior AB + bladder walls = bladder Exstrophy – >Expose bladder surface
– > Adenocarcinoma