Renal Pathology Flashcards

1
Q

Nephrotic syndrome

A

Chronic
Massive proteinuria - albumin selective
Oedema

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2
Q

Blood changes in Nephrotic syndrome

A

Hypoalbuminaemia

Hyperlipidaemia

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3
Q

Nephritic syndrome

A

Acute
Variable unselective proteinuria
Haematuria

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4
Q

Consequences of Nephritic syndrome

A

Mild oedema
Oligouria
HTN

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5
Q

Blood changes in Nephritic syndrome

A

Azotaemia - high nitrogen

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6
Q

Pathophysiology of Nephrotic syndrome

A

Damage to glomerular filtration barrier
Loss of foot processes
No inflammation

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7
Q

Types of glomerular disease (inc. Nephrotic syndrome)

A

Minimal change disease
Focal segmental glomerulosclerosis
Membranous glomerulonephritis

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8
Q

Pathophysiology of Nephritic syndrome

A

Inflammation, vascular and epithelial damage

+/- glomerular cell proliferation

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9
Q

Types of Nephritic syndrome

A

1) Proliferative glomerulonephritis

2) Membranoproliferative (mesangiocapillary) glomerulonephritis

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10
Q

Proliferative glomerulonephritis

A

Post infective

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11
Q

Membranoproliferative (mesangiocapillary) glomerulonephritis

A

Diffuse
Crescentic glomerulonephritirs
Lupus nephritis

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12
Q

Causes of golmerulonephritis

A

Primary

Secondary to systemic disease

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13
Q

Pathophysiology of glomerulonephritis

A

Immunological

Deposition of immune complex in glomerular capillary wall

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14
Q

Ix for glomerulonephritis

A

Immunohistochemistry:

  • Local deposition of circulating immune complexes
  • Anti-glomerular basal membrane antibodies
  • Antibodies against glomerular component
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15
Q

Causes of Acute tubular necrosis

A

Ischaemia
Toxic drug injury - statin
DIC
Urinary obstruction

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16
Q

Presentation of Acute tubular necrosis

A

Acute renal failure

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17
Q

Causes of Tubulointersitial nephritis

A

Acute pyelonephritis
Chronic pyelonephritis
Drugs - analgesics

18
Q

Presentation of acute pyelonephritis

A

Fever

Elevated creatinine

19
Q

Histology of chronic pyelonephritis

A

Dilated colloid filled tubules

20
Q

Post mortem features of chronic pyelonephrits

A

Irregularly depressed/scarring of kidneys

21
Q

Hypertensive kidney disease

A

Benign nephrosclerosis - focal ischaemia

Malignant HTN and accelerated nephroscerlosis

22
Q

Types of Cystic kidney disease

A

Malformative/congenital
Acquired
Hereditary

23
Q

Malformative cystic kidney disease

A

Multicystic renal dysplasia

Medullary sponge kidney

24
Q

Acquired cystic kidney disease

A

Acquired renal cystic disease - often post dialysis

Simple cysts

25
Hereditary cystic kidney disease
Autosomal dominant polycystic kidney disease Nephronophthisis
26
Nephronophthisis
Medullary cystic kidney disease complex
27
Autosomal dominant polycystic kidney disease
Bilateral | Presents in middle age
28
Presentation of Autosomal dominant polycystic kidney disease
``` Haematuria UTI Abdo mass HTN Cysts in liver, pancreas, lung Cerebral aneurysms ```
29
Complication of Autosomal dominant polycystic kidney disease
Ruptured berry aneurysm
30
Mx of Autosomal dominant polycystic kidney disease
Supportive Treat HTN Renal replacement therapy
31
Causes of CKD
DM | HTN
32
Stages of CKD and eGFR
1) > 90 2) 60-90 3A) 45-60 3B) 30-45 4) 15-30 5) < 15
33
Nephrolithiasis
Stone formation | In kidney or renal tract
34
Types of kidney stone
Calcium oxalate Triple phosphate Urate Cystine
35
Renal tumours
Wilm's tumour - childhood Benign - papiliary adenomas Malignant - RCC, TCC
36
Renal cell carcinomas (RCC) RFs
Smoking HTN Heavy metals Von Hippel Lindau syndrome
37
Histotypes of RCC
Clear cell Papiliary Chromophobe
38
Sx of RCC
``` Polycythaemia Hypercalcaemia Cushing's Haematuria Back pain ```
39
Benign Bladder tumours
Papilloma
40
Low malignant potential Bladder tumours
Papillary urothelial neoplasm
41
Malignant Bladder tumours
Low grade papillary urothelial carcinoma | High grade urothelial carcinoma
42
Bladder tumour RFs
``` Smoking Dye industry Long term analgesic use Schistosomiasis - SCC Cyclophosphamide ```