urological pathology Flashcards

1
Q

what are urinary calculi

A

Crystal aggregates that form in the renal collecting ducts
May be deposited anywhere in the urinary tract

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2
Q

epi of urinary calculi

A

common

men 3x mor e

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3
Q

composition of renal stones

A
  • Calcium Oxalate (Weddellite) – 75%
  • Magnesium Ammonium Phosphate (Struvite) – 15%
  • Uric Acid – 5%
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4
Q

what are ca oxalate stones and potential mechanisms for them

A

related to hyperca
* absorptive hyperca - excessive ca absorption from the gut
* renal hyperca - impaired absorption of ca in the prox renal tuble
* hyperca - primary hyperpareathyroidism - rare !

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5
Q

what are triple stones

A

Magnesium ammonium phosphate stones

can become very big - staghorn calculi

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6
Q

mech of triple stones

A

Form as a consequence of infection with urease-producing organisms

eg Proteus sp.

-> Ammonia alkalinises urine
-> precipitation of magnesium ammonium phosphate salts follows

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7
Q

mech of uric acid calculi

A

hyperuricaemia - but many that have these stones dont have hyperuricaemia
* gout
* rapid turnover

tendency for some people to produce slightly acidic urine

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8
Q

complications of urinary calculi

A

depends on size

small and stay in kidney:
* asx
* haematuria
* recurrent UTI

out of kidney and small
* intense pain/colic - kidney impacted as stone gets stuck at Pelvi-ureteric junction, pelvic brim, vesico-ureteric junction

large and in kidney
* obstruction
* risk of infection - stagnant urine
* CKD - increased pressure
* kidney atrophy around stone

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9
Q

what are the benign renal neoplasms

A

papillary adenoma
renal oncocytoma
angiomyolipoma

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10
Q

what is papillary adenoma and features

A

benign renal neoplasm

made of papillae and/or tubules

by definition 15mm or less

well circumscribed

chr:
* trisomy 7
* trisomy 17
* loss of Y chr

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11
Q

presention of papillary adenoma

A

incidental finding at nephrectomies and autopsy

esp in CKD/acquired cystic disease

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12
Q

what is renal oncocytoma and features

A

Benign epithelial kidney tumour composed of oncocytic cells

Well-circumscribed

Usually sporadic

Can be seen in Birt-Hogg-Dubé syndrome

Made of pink oncocytic cells - Pink because mitochondria
Mohogony brown with central scar

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13
Q

presentation of renal oncocytoma

A

incidental

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14
Q

what are angiomyolipomas

A

benign mesenchymal kidney tumour

made of
* thick walled bv
* sm
* fat

Derived from perivascular epithelioid cells
Mostly sporadic
Can be seen in tuberous sclerosis – most people that have it don’t have tuberous sclerosis

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15
Q

presentation of angiomyolipoma

A

incidental

> 4cm
* flank pain
* haemorrhage -> shock

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16
Q

epidemiology of renal cell ca

A

common
more in developed
more men

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17
Q

RF for RCC

A

Smoking
Hypertension
Obesity
Long-Term Dialysis
Genetic Syndromes – von Hippel Lindau

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18
Q

what is RCC

A

malignant epithelial kidney tumour

Various subtypes are recognised
* Clear Cell Renal Cell Carcinoma (70%)
* Papillary Renal Cell Carcinoma (15%)
* Chromophobe Renal Cell Carcinoma (5%)
* Remaining 10% are various rare subtypes

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19
Q

presentation of RCC

A

painless haematuria

incidental

small proportion - mets

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20
Q

what are clear renal cell ca

A

epithelial tumour

nests of clear cells set in delicate capillary vascular network

macro = golden yellow tumour, haemorrhagic areas

loss of chr 3p

Squished normal kidney inc glomerulus On R – clear cells pushing way in
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21
Q

what is papillary renal cell ca

A

epithelial

composed of papillae and/or tubules

>15 mm (counterpart is papillary ademoma)
macro = fragile, friable brown tumour

chr:
* trisomy 7
* trisomy 17
* loss of Y chr

subdivided:
* Type 1 = well defined and show consistent genetic loss
* Type 2 – more heterogenous - tend to have worse Px but because heterogenous cant tell which ones will be

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22
Q

what are chromophobe RCC

A

epithelial
sheets of large cells that display
* distinct cell borders
* reticular cytoplasm
thick walled vascular network

heterogenous

macro - well circumscribed solid brown tumour
plant like - because of well defined borders

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23
Q

px of RCC

A

5yr survival 60%
staging and grading are important
grade 1-4

for clear cell there is also risk of progression index - leibovich risk model (low, intermediate, high)

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24
Q

what is Wilm’s tumour

A

nephroblastoma

25
features of wilm's tumour
Malignant **triphasic** kidney tumour of childhood * Blastema (small round blue cells) * Epithelial * Stromal *2nd most common tumour of childhood*
26
presentation of Wilm's tumour
abdo mass 2-5yrs
27
px of Wilm's
Proportion and appearance of components (blastema, epithelial, stromal) give idea of Px 95% excellent px
28
what are urothelial carcinomas
transitional cell carcinomas malignant neoplasms arising in urothelial tract - bladder, renal pelvis, ureters Three main subtypes * Non-Invasive Papillary Urothelial Carcinoma * Infiltrating Urothelial Carcinoma * Flat Urothelial Carcinoma in-situ
29
epi and RF for urothelial carcinoma
smoking aromatic amines
30
presentation of urothelial tumours
haematuria - *do cystoscopy*
31
summarise non-invasive papillary urothelial carcinoma
**frond like** growths low and high grade based on nuclear atypia low grade have low chance of progression to invasive high = higher risk unstable - genetic aberrations include RB TP53
32
summarise infiltrating urothelial carcinoma
displays invasive behaviour Treatment based on depth of invasion * Lamina propria – local excision/chemo etc * Muscularis propria – cystectomy = loss bladder, ureter, prostate, +- urethera Can maintain true to appearance, can look like other cancers, can produce and secrete other things – once they start to invade the morphology v diverse – more diverse = worse px
33
what are flat urothelial carcinoma in situ
high grade in situ invisible or reddish Flat urothelial lesion with unequivocal high grade features High risk of progression
34
what is BPH
**Benign enlargement of prostate as a consequence of increase in cell number** **Very common** – symptomatic in 25% of men by age 80 Histologically present in 90% of men by age 80
35
aetiology of BPH
unclear increased oestrogen levels with age -> may induce androgen receptors -> hyperplasia
36
rx of BPH
alpha blockers and 5a reductase inhibitors transurethral resection - core out centre of prostate to ease flow of urine
37
presentation of BPH
“Lower Urinary Tract Symptoms” * Frequency * Nocturia * Urgency * Hesitancy * Poor flow * Terminal Dribbling urinary tract infection - incomplete emptying acute urinary retention renal failure (from poor flow -> bilateral hydronephrosis)
38
what is prostatic adenocarcinoma and the aetiology
malignant epithelial prostate tumour red meat increased risk if 1st degree relative ethnic differences arise from prostatic intraepithelial neoplasia mutation in *(not traditional oncogenes so we don’t really know why people get them)* * PTEN * AMACR * GST-pi * p27
39
epi of prostatic adenocarcinoma
common Less prominent (but important) cause of cancer-related death
40
presentation of prostatic adenocarcinoma
asx dx on biopsy after raised PSA or DRE LUTS - but less than BPH because the cancer is more peripheral so sx are late Rarely present with metastatic disease * Pathological fracture – mets are sclerotic not lytic
41
px indicator for prostatic cancer
**Gleason score** Expressed as x + y = z **Two most common patterns (or most common pattern and worst pattern in biopsy setting** – don’t want to underestimate how bad it could be because only have a small biopsy) Patterns range from 1-5 1 and 2 rarely if ever diagnosed so scores typically range from 6-10 **Higher scores correlate with aggressive behaviour** High volume tumours scoring 8-10 in particular Grade grouping used as well
42
How distinct the glands are and how much it resembles still Grade 3 – simplified but distinct glands How distinct the glands are and how much it resembles still Grade 3 – simplified but distinct glands
43
gleason grade 4
have fusion of glands
44
gleason grade 5
Pattern 4 + necrosis Frank sheets of tumour cells
45
what are testicular germ cell tumours
Tumours of the testis arising from germ cells Five histological subtypes Single tumour may be purely one subtype or contain a mixture of multiple subtypes Malignant tumours arise from **Germ Cell Neoplasia in-situ** * Process likely begins in **foetal life** * Amplification of **i12p**
46
epi and RFs for testicular germ cell tumours
90% of testicular tumours 20-45yrs RF * undescended testes * LBW/SGA
47
presentation of testicular germ cell tumours
painless lump mets * Back pain – lymphatic drainage is para-aortic * Cough – lung mets * Dyspnoea
48
seminoma
germ cell testicular tumour: Clear cells prominent lymphoid infiltrate Fibrous septae Common
49
embryonal germ cell testicular ca
High grade Necrotic Nasty
50
post pubertal teratoma - germ cell testicular tumour
From germinal layers trying to produce different tissues Malignant Each component can develop its own malignancy – ie if tumour trying to become lung, it can then become lung cancer
51
yolk sac tumour - testicular germ cell tumour
Try to replicate primitive structures Smaller cells, lace like growth patterns Look different
52
testicular choriocarcinoma - germ cell tumour
Cytotrophoblast cells Multinucleated cells – syncitiotrophoblast cells Impacts on Px badly
53
mx of germ cell tumour
Highly sensitive to **platinum-based chemotherapy** regimes
54
Px of germ cell tumour
**Prognosis excellent** Five year survival is 98% in most countries Poor if have bad types and present with mets
55
summarise the testicular non-germ cell tumours
less common than germ cell tumours **Lymphoma** * **Older** men, 5% of all testicular tumours * Highly **aggressive**; poor survival rates **Leydig Cell Tumour** * 3% of all testicular tumours * May present with **precocious puberty** if pre-pubertal * Usually **benign** **Sertoli Cell Tumour** * 1% of testicular tumours * 90% are **benign**
56
list some paratesticular diseases
Epididymal cyst – benign Epididymitis * Usually related to C. trachomatis or N. gonnorrhoeae in men under 35; * E. coli in men over 35 Varicocele - Dilated venous plexus Hydrocele - Fluid between layers of tunica vaginalis Adenomatoid Tumour * Small tubules lined by mesothelial cells * Uncommon
57
what are the penile diseases
Lichen Sclerosus / Balanitis Xerotica Obliterans * Inflammatory condition that causes phimosis * RF for penile ca – rare Zoon’s balanitis * Inflammatory condition that causes red areas Condylomas -HPV 6 and 11 Peyronie’s Disease * Scarring , inflammation, thickening of corpus cavernosa * -> penis curve Penile carcinoma * Rare, elderly men * Smoking, HPV, chronic Lichen Sclerosus are risk factors
58
urethral diseases
Urethritis * Non specific or N. gonorrhoeae (purulent discharge), C. trachomatis Prostatic Urethral Polyp * Papillary lesion in prostatic urethra Urethral Caruncle * Inflammatory mass * common lesion at urethral meatus in women Urethral Carcinoma * Rare, more common in women, usually squamous cell carcinoma Malignant Melanoma - V Rare
59
scrotal diseases
Epidermoid Cyst * Common * Invagination of skin – cyst surrounded by skin and filled with keratin when old and contents calcify -> Scrotal Calcinosis * Rare; may be related to old epidermoid cysts Angiokeratomas * Benign vascular lesions * Tumour with vascular network * Keratin and skin on surface has become thickened Fournier’s Gangrene * Necrotising fasciitis; * mortality of 15-20% Important to recognise quickly Scrotal squamous cell carcinoma * Very rare * Historical interest; chimney sweep