Other Renal Pathology Flashcards

1
Q

State three differentials for asymptomatic haematuria

A

Thin basement membrane disease (benign familial haematuria), IgA nephropathy (Berger disease), Alport syndrome (hereditary nephritis)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Describe acute tubular necrosis (ATN)

A

Damage to tubular epithelial cells causing cell shedding, blocking the renal tubules and leading to reduced blood flow and increased haemodynamic pressure in the nephron. This reduces the pressure across the basement membrane, leading to acute renal failure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the most common cause of acute renal failure?

A

Acute tubular necrosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

State the two main causes of acute tubular necrosis

A

Hypovolaemia, nephrotoxins (e.g. aminoglycosides, NSAIDs, radiographic contrast agents, myoglobin, heavy metals)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Describe the histology of acute tubular necrosis

A

Necrosis of short segments of renal tubules

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

State the four types of tubulointerstitial nephritis

A

Acute pyelonephritis, chronic pyelonephritis, acute interstitial nephritis, chronic interstitial nephritis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Define acute pyelonephritis

A

Bacterial infection of the kidney, most commonly ascending infection with E coli

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Describe the symptoms of acute pyelonephritis

A

Fever, chills, sweats, flank pain, renal angle tenderness, leucocytosis, urinary frequency, dysuria, haematuria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Define chronic pyelonephritis

A

Chronic inflammation and scarring of the parenchyma caused by recurrent and persistent bacterial infection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

State the two main causes of chronic pyelonephritis

A

Chronic obstruction (e.g. posterior urethral valves, renal calculi), urine reflux

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Define acute interstitial nephritis

A

A hypersensitivity reaction, usually to a drug, occurring days after exposure

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Describe the clinical features of acute interstitial nephritis

A

Fever, skin rash, haematuria, proteinuria, eosinophilia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Describe the clinical features of chronic interstitial nephritis

A

Asymptomatic

Late in disease: hypertension, anaemia, proteinuria, haematuria

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

State the cause of chronic interstitial nephritis

A

Long-term analgesic consumption in the elderly

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Name two thrombotic microangiopathies

A

Haemolytic-uraemic syndrome (HUS), thrombotic thrombocytopaenic purpura (TTP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Describe the characteristics of thrombotic microangiopathies

A

Thrombosis, and a triad of microangiopathic haemolytic anaemia (MAHA), thrombocytopaenia, and renal failure

17
Q

State three differences between HUS and TTP

A

Epidemiology: HUS more common in children, TTP more common in adults
Thrombi: HUS confined to kidneys, TTP thrombi throughout circulation (especially CNS)
Renal: HUS causes renal failure, TTP usually no renal failure

18
Q

Describe the pathophysiology of thrombotic microangiopathies

A

The platelet surface protein ADAMTS3 mediates widespread fibrin deposition in vessels, leading to the formation of platelet-fibrin thrombi which damage passing platelets and red blood cells, leading to platelet and red blood cell destruction

19
Q

Describe the clinical features of thrombotic microangiopathies

A

Bleeding, petechiae, haematemesis, melaena, pallor, jaundice

20
Q

How are thrombotic microangiopathies diagnosed?

A

Low haemoglobin, low platelets, increased bilirubin, increased reticulocyte count, increased lactate dehydrogenase, fragmented red blood cells on blood smear, Coomb’s test negative (excludes autoimmune haemolytic anaemia)

21
Q

Define acute renal failure

A

A rapid loss of renal function manifesting as increased serum creatinine and urea

22
Q

State at least 3 complications of acute renal failure

A

Metabolic acidosis, hyperkalaemia, fluid overload, hypertension, hypocalcaemia, uraemia

23
Q

What is the most common cause of acute renal failure?

A

Hypoperfusion

24
Q

State three renal causes of acute renal failure

A

Acute tubular necrosis, acute glomerulonephritis, thrombotic microangiopathy

25
Q

State at least three post-renal causes of acute renal failure

A

Renal stones, tumours, prostatic hypertrophy, retroperitoneal fibrosis - all cause obstruction

26
Q

Define chronic renal failure

A

Progressive, irreversible loss of renal function characterised by prolonged symptoms and signs of uraemia (fatigue, itching, anorexia, eventually confusion)

27
Q

State the five most common causes of chronic renal failure, in order

A

Diabetes, glomerulonephritis, hypertension/ vascular disease, reflux nephropathy, polycystic kidney disease

28
Q

State the GFR for each stage of chronic renal failure

A

1: >90
2: 60-89
3: 30-59
4: 15-29
5: <15/ on renal replacement therapy

29
Q

Which genes are involved in adult polycystic kidney disease? (APCKD)

A

85% of cases: PKD1 on chromosome 16, encoding polycystin-1

15% of cases: PKD2 on chromosome 4, encoding polycystin-2

30
Q

Describe the pathological features of adult polycystic kidney disease

A

Large multicystic kidneys with destroyed renal parenchyma, berry aneurysms. In PDK1, liver cysts

31
Q

Describe the clinical features of adult polycystic kidney disease

A

Usually due to complications: Haematuria, flank pain, UTI

32
Q

Describe the clinical features of lupus nephritis

A

Depending on site of immune complex deposition: urinary abnormalities, acute renal failure, nephrotic syndrome, progressive chronic renal failure

33
Q

Describe class I lupus nephritis (minimal mesangial)

A

Immune complexes but no structural alteration

34
Q

Describe class II lupus nephritis (mesangial proliferative)

A

Immune complexes and a mild-moderate increase in mesangial matrix and cellularity

35
Q

Describe class III lupus nephritis (focal)

A

Active swelling and proliferation in less than half the glomeruli

36
Q

Describe class IV lupus nephritis (diffuse)

A

Active swelling and proliferation in more than half the glomeruli

37
Q

Describe class V lupus nephritis (membranous)

A

Subepithelial immune complex deposition

38
Q

Describe class VI lupus nephritis (advanced sclerosing)

A

Complete sclerosis of >90% of the glomeruli

39
Q

Describe the clinical features of renal cell carcinoma

A

Costovertebral pain, palpable mass, haematuria.

Paraneoplastic syndrome causes polycythaemia, hypercalcaemia, hypertension, Cushing’s syndrome, and amyloidosis