Urinary tumours Flashcards
Papillary adenoma
insignificant, small, discrete and benign
Angiomyolipoma
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
Angiomyolipoma histological features
- blood vessels ensheathed by smooth muscles
- clusters of adipocytes
Oncocytoma
- originates from IC of collecting duct
- usually solitary
- large eosinophilic cells, with small round nuclei and large nucleoli
Presentations of renal cell carcinoma
Classical triad: loin pass, mass and haematuria
Paraneoplastic syndrome: unexplained fever, polycythaemia
metastasis may present before symptoms
Renal cell carcinoma, clear cell type
- 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
Papillary renal cell carcinoma
- 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
Chromophobe renal cell carcinoma
- 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
Collecting duct carcinoma
- Originates from collecting duct, usually medulla
- aggressive, with high grade nucleus and necrosis
- poor prognosis with early metastasis
Urothelial carcinoma of renal pelvis
- 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
Nephroblastoma/ Wilms tumour
- associated with WT-1/-2 gene deletion or mutation
- might have bilateral: synchronous or metachronous
- same presentation and spreading method as renal cell carcinoma
Histological features of nephroblastoma
triphasic: blastemal (undifferentiated round cells), stromal (spindle cells), epithelial (columnar epithelial cells)
Presentations and features of urinary bladder tumours
- usually in middle aged men (more than female)
- usually urothelial carcinoma, others include squamous cell carcinoma and adenocarcinoma
- painless gross haematuria
Benign bladder tumour
Urothelial papilloma and inverted papilloma
- normal urothelium
- finger like papillae with fibrovascular core
- single and small usually
Malignant bladder tumour
papillary carcinoma and flat carcinoma (can be invasive/ non-invasive)