Inflammation in the Kidneys Flashcards

1
Q

What is the name of the cell with lots of ‘legs’ which create the pores in the glomerulus and allow for the filtrate of protein but the retention of proteins?

A

Podocytes

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2
Q

What triggers the classical complement pathway?

A

Antigen antibody complexes

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3
Q

What triggers the alternative complement pathway?

A

Pathogen cell membranes

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4
Q

What is glomerulonephritis?

A

Inflammation of the glomeruli usually caused by immunological mediated injury to the glomeruli

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5
Q

What 2 mechanisms cause glomerulonephritis?

A

1) deposition of immune complexes (antibody:antigen complexes)
2) deposition of anti-glomerular basement membrane antibodies

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6
Q

How may glomerulonephritis present?

A

Hypertension

Microscopic haematuria

Proteinuria

Nephrotic Syndrome (proteinuria, low albumin, high lipids, oedema)

AKI (reduced GFR)

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7
Q

What are renal bruits and when are they heard?

A

Vascular sounds caused by turbulent flow, in this incidence caused most likely by renal artery stenosis

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8
Q

What is the most common type of glomerulonephritis?

Explain this disease.

Therefore, what type of hypersensitivity reaction is this disease?

A

IgA nephropathy (Berger disease) (type 3 hypersensitivity)

IgA (mucosal) immune complex accumulation and deposition in the kidneys

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9
Q

Name a condition similar to IgA nephropathy (Berger’s)?

A

Henoch-scholein purpura - a form of small vessel vasculitis

IgA immune complexes depositing in the vasculature giving an associated rashes

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10
Q

What are some differences between IgA nephropathy and HSP?

A

HSP
= systemic (therefore leucocytoclasic vasculitis rash and other signs)
= favours younger children

IgA nephropathy
= kidneys only
= favours young adults

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11
Q

What is a typical presentation of IgA nephropathy and HSP?

A

Hypertension

Haematuria

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12
Q

What symptom can nephrotic syndrome present with?

Why does it present with this?

A

Oedema due to a protein leak in the kidney

Proteins = main oncotic pressure maintainer

Water therefore moves into tissues where oncotic gradient is higher

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13
Q

What are the most common causes of nephrotic syndrome in children and by what %?

And in adults?

A

FSGS (focal segmental glomerulosclerosis) (35% in adults)

Minimal change disease (90% in kids, 10% in adults)

And in adults - membranous nephropathy (33% in adults) added into the Ddx, along with amyloid and diabetes

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14
Q

Differentiate between AL Amyloidosis and Multiple Myeloma.

A

AL Amyloidosis (light chain)
= proteins misfolded and lodged in extracellular tissue space
= can be systemic = multiple organs
= Ig light chain is the misfolded protein which is deposited

Multiple Myeloma
= Bone marrow produced too many light chains compared to heavy
= build up in tissues
= has bone breakdown (so calcium levels high)

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15
Q

What are some complications of nephrotic syndrome?

A

Hypovolaemia = as fluid is in tissues not circulating

VTE = risk higher

Infections as Ig are lost in urine

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16
Q

What is nephrotic syndrome treatment?

A

Diuretics and ACE inhibitors = to correct fluid balance

VTE prophylaxis (anticoagulation)

Statin = lowers hyperlipidaemia

Renal biopsy to work out underlying cause

17
Q

Explain the pathology of minimal change disease in terms of testing and symptoms.

A

Sudden onset oedema in children

NORMAL light microscopy

Podocyte foot changes in electron microscopy was

18
Q

Explain the pathology of FSGN in terms of testing and symptoms.

A

Lesion, NOT a disease

Light microscopy shows changes = focal and segmental (hence name) mesangial collapse areas and sclerosis

19
Q

Explain the pathology of membranous nephropathy in terms of testing and symptoms.

A

Glomerular BM thickening

20
Q

What is the first step in hyperkalaemia treatment?

A

Calcium glauconite to protect the heart

21
Q

What are signs of ANCA vasculitis?

A

Pulmonary oedema

AKI

22
Q

What is another name for goodpastures Syndrome?

A

Anti-GBM disease

23
Q

What is a bench Jones protein?

A

An Ig light chain