Urinary tumours Flashcards

1
Q

Papillary adenoma

A

insignificant, small, discrete and benign

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2
Q

Angiomyolipoma

A

associated with tuberous sclerosis

  • large ones may lead to haemorrhage
  • increase in size during pregnancy
  • usually find in CT scan with fat attenuation
  • bilateral and multiple
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3
Q

Angiomyolipoma histological features

A
  • blood vessels ensheathed by smooth muscles

- clusters of adipocytes

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4
Q

Oncocytoma

A
  • originates from IC of collecting duct
  • usually solitary
  • large eosinophilic cells, with small round nuclei and large nucleoli
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5
Q

Presentations of renal cell carcinoma

A

Classical triad: loin pass, mass and haematuria
Paraneoplastic syndrome: unexplained fever, polycythaemia
metastasis may present before symptoms

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6
Q

Renal cell carcinoma, clear cell type

A
  • mostly sporadic, might be associated with Von Hippel-Lindau syndrome (dominant)
  • some show sarcomatoid changes
  • clear cells, some might have eosinophilic or granular cytoplasm
  • capillary network surround the tumour cells
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7
Q

Papillary renal cell carcinoma

A
  • mostly sporadic, some associated with hereditary papillary renal cancer syndrome or trisomy 7
  • thought to be from distal tubule
  • cuboidal or low columnar cells in papillary arrangement
  • foam cell papillary core
  • highly vascular stroma
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8
Q

Chromophobe renal cell carcinoma

A
  • originate from the IC of collecting duct
  • associated with monosomy
  • better prognosis than clear cell type and papillary
    Histology:
  • pale eosinophilic cells with prominent cell membrane and halos around nucleus
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9
Q

Collecting duct carcinoma

A
  • Originates from collecting duct, usually medulla
  • aggressive, with high grade nucleus and necrosis
  • poor prognosis with early metastasis
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10
Q

Urothelial carcinoma of renal pelvis

A
  • very similar to urinary bladder tumours, might involve the ureters and bladder
  • Small upon presentation: haematuria, obstruction leading to flank pain and hydronephrosis
  • invasion of renal pelvis wall and calyces
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11
Q

Nephroblastoma/ Wilms tumour

A
  • associated with WT-1/-2 gene deletion or mutation
  • might have bilateral: synchronous or metachronous
  • same presentation and spreading method as renal cell carcinoma
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12
Q

Histological features of nephroblastoma

A

triphasic: blastemal (undifferentiated round cells), stromal (spindle cells), epithelial (columnar epithelial cells)

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13
Q

Presentations and features of urinary bladder tumours

A
  • usually in middle aged men (more than female)
  • usually urothelial carcinoma, others include squamous cell carcinoma and adenocarcinoma
  • painless gross haematuria
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14
Q

Benign bladder tumour

A

Urothelial papilloma and inverted papilloma

  • normal urothelium
  • finger like papillae with fibrovascular core
  • single and small usually
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15
Q

Malignant bladder tumour

A

papillary carcinoma and flat carcinoma (can be invasive/ non-invasive)

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16
Q

Papillary carcinoma

A
  1. papillary urothelial neoplasm with little malignant potential
  2. Papillary urothelial carcinoma, low grade
  3. high grade

Thickened urothelium, and bigger in size
Can spread/seed by implantation

17
Q

Grading of papillary carcinoma

A
Increased cellularity
Nuclear pleomorphism
High mitotic rate
Loss of cell polarity
Poor differentiation
Nuclear crowding

determines the probability of invasion

18
Q

Flat carcinoma

A

Default high grade, also known as urothelial carcinoma in situ
commonly multifocal
Cytological malignant cells with flat apppearance

19
Q

Depth of invasion/ staging

A

T1 lamina propria invasion

T2/3 Muscularis propria

20
Q

Treatment of bladder cancer

A
  1. urothelial neoplasm with low malignant potential or low grade- transurethral resection
  2. high grade or T1 invasion- transurethral resection and intravesicle instillation of BCG
  3. T2 invasion- radical cystectomy
21
Q

Urine cytology

A
  • used in screening or follow up after transurethral resection
  • low sensitivity for the low grade carcinoma
  • FISH used to detect aneuploidy