Pathology 2 Flashcards

1
Q

What is agenesis?

A

absence of one or both kidneys

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2
Q

What is hypoplasia of the kidneys?

A

small kidneys but normal development

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3
Q

What are horseshoe kidneys?

A

fusion at either pole- usually inferior

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4
Q

What is a duplex kidney?

A

kidney with more than one ureter

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5
Q

What are simple cysts?

A

very common, usually no functional disturbance

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6
Q

What happens in infantile type polycystic?

A

uniform bilateral renal enlargement, elongated cysts with dilatation of medullary collecting ducts; no gross distortion of the kidney

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7
Q

What is the inherintance of infantile polycystic kidneys?

A

autosomal recessive

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8
Q

What are infantile polycystic kidneys associated with?

A

congenital hepatic fibrosis

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9
Q

What is the inheritance of adult polycystic disease?

A

autosomal dominant

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10
Q

When does adult polycystic disease usually present?

A

middle adult life

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11
Q

What does adult polycystic disease present with?

A

abdo mass; haematuria; HT; CRF

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12
Q

What is seen with adult polycystic disease?

A

massive bilateral renal enlargement; mulitple cysts of varying size- distortion of reniform shape

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13
Q

What is adult polycystic disease associated with?

A

cysts in liver, pancreas and lung; Berry aneursysms in circle of willis

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14
Q

What does a berry aneurysm result in?

A

subarachnoid haemorrhage

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15
Q

What ar ethe types of benign renal tumours?

A

fibroma; adenoma; angiomyolipoma; JGCT

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16
Q

Describe fibromas?

A

common white nodules originating from the medulla

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17
Q

Describe adenomas?

A

yellowish nodules <2cm of cortical origin

18
Q

Describe angiomyolipomas?

A

mixture of fat; muscle and blood vessels- can be mulitple and bilateral

19
Q

What disease are angiomyolipomas assocaited with?

A

tuberous sclerosis

20
Q

What does JGCT stand for?

A

juxtaglomerular cell tumour

21
Q

What do JGCTs cause?

A

secondary HT due to production of renin

22
Q

What are the types of malignant renal tumours?

A

nephroblastoma; urothelial carcinomas; renal cell carcinoma

23
Q

What do nephroblastomas arise from?

A

residual primitive renal tissue

24
Q

How do nephroblastomas present?

A

abdominal mass in child

25
Where do renal cell carcinomas arise from?
renal tubular epithlium
26
What is the commonest primary renal tumour in adults?
renal cell carcinoma
27
How does renal cell carcinoma present?
abdo mass; haematuria; flank pain
28
What can be seen on bloods with renal cell carcinoma?
polycythaemia; hypercalcaemia (ectopic PTH)
29
Who gets renal cell carcinomas?
55-60 years; M:F 2:1
30
How do renal cell carcinomas appear pathologically?
large well circumscribed mass in cortex; yellow with solic, cystic, necrotic and haemorrhagic areas
31
What indicates bad prognosis with RCC?
renal vein extension- can extend into vena cava to RA
32
How does RCC first spread?
blood
33
What is the commonest type of RCC?
clear cell type
34
Where is transitional epithlium present in the urine system?
pelvicalycael system to urethra
35
What is the commonest bladder tumour?
transitional cell carcinoma
36
What is the commonest symptom of TCC?
haematuria
37
Where do the majority of TCCs arise?
trigone- ureteric obstruction
38
What is the difficulty with TCCs?
recurrence is frequent
39
What is the commonest malignent bladder tumour in children?
embryonal rhabdomyosarcoma
40
When do squamous carcinomas arise?
post calculi (squamous metaplasia)