Glomerulonephritis Flashcards

(37 cards)

1
Q

What two main groups can glomerulonephritis be divided into?

A

Proliferative
Non - proliferative

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2
Q

What is non - proliferative glomerulonephritis?

A

Damage to the podocytes

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3
Q

What is proliferative glomerulonephritis?

A

Damage to endothelial/mesangial cells

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4
Q

Examples of non proliferative Gn

A

Minimal change disease

Focal segmental glomerulosclerosis

Membranous Gn

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5
Q

Examples of proliferative Gn

A

Membranoproliferative Gn

IgA nephropathy

Post-streptococcal Gn

Rapidly progressive Gn (crescentic) — either ANCA +ve or ANCA -ve

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6
Q

What are ANCA +ve vasculitic disorders?

A

Microscopic polyangiitis –
p-ANCA

Wegener’s granulomatosis (GPA) –
c-ANCA

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7
Q

Goodpasture’s disease is ANCA +ve. True/false

A

False. ANCA - ve

Often detected by renal biopsy or blood test for anti-GBM antibodies

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8
Q

Most common cause of Gn (aka nephritic disease) in adults

A

IgA nephropathy

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9
Q

Most common cause of nephrotic disease in adults

A

Focal segmental glomerulosclerosis

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10
Q

What skin condition is IgA nephropathy associated with?

A

HSP (henoch - schonlein purpura)

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11
Q

Most common nephrotic syndrome in children

A

Minimal change disease

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12
Q

What are some associated causes of focal segmental glomerulosclerosis?

A

HIV, heroin use and obesity

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13
Q

What is the main difference between post - streptococcal Gn and IgA nephropathy?

A

IgA nephropathy usually occurs 24-48 hrs after URTI

Post streptococcal Gn usually occurs a few weeks after URTI

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14
Q

How is proteinuria quantified?

A

By calculating the urine protein:creatinine ratio. Measured over 24 hours.

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15
Q

Chronic GN is the 2nd most common cause of end-stage renal failure (CKD). What is the most common cause?

A

Diabetic nephropathy, a microvascular complication of diabetes mellitus.

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16
Q

Glomerulonephritis is caused by infection. True/false.

A

False. It is immune-mediated (autoimmune).

17
Q

2nd most common cause of nephrotic syndrome in adults?

A

Membranous Glomerulonephritis

18
Q

How is minimal change disease shown on microscopy and how is it treated?

A

Abnormal Podocytes are seen on electron microscopy. Usually treated with supportive care and prednisolone.

19
Q

Focal segmental glomerulosclerosis presents with nephritic syndrome and is treated with steroid. True/false.

A

False. Focal segmental glomerulosclerosis presents with nephrotic syndrome and steroids are often ineffective.

20
Q

What is membranous GN characterised by and what is it caused by?

A

Thickened glomerular basement membrane due to immune complex deposition at the basement membrane and is idiopathic.

21
Q

What antibody is membranous GN associated with?

A

Anti-PLA2R (present in 70% of cases).

22
Q

What characteristic does rapidly progressive Glomerulonephritis have?

A

Crescentic - presence of crescents (epithelial cell extracapillary proliferation).

23
Q

List primary and secondary causes of membranoproliferative GN

A

Primary: immune-mediated

Secondary: SLE and Hep

24
Q

Membranoproliferative GN usually progresses to end stage renal failure. True/false

25
Wegeners granulomatosis (GPA) is c-ANCA positive and microscopic polyangiitis is p-ANCA positive. True/false.
True
26
GPA presentation?
Vasculitis Affects lungs, kidneys and other organs. C-ANCA +ve Treat with steroids + cyclophosphamide
27
Microscopic polyangiitis presentation?
Small vessel vasculitis P-ANCA +ve Treat with long term steroids +/- cytotoxic agents
28
Another name for Anti-GBM disease
Goodpasture’s disease
29
Goodpasture’s disease presentation?
Presence of autoimmune Anti-GBM antibody in the blood Glomerulus and lungs are affected Haematuria (blood in urine) and haemoptysis (coughing up blood) Treat with steroids +/- steroid sparing agents
30
What bacteria is involved in post - infectious (post -streptococcal) GN?
Strep pyogenes
31
What is treatment for post -strep GN?
Supportive treatment (diet changes etc) Resolves over 2-4 weeks
32
Main differences between nephrotic and nephritic syndrome.
Nephrotic: Urinary albumin > 3g/day Hypoalbuminaemia Periorbital oedema Appearance of “frothy urine” due to high protein lost in urine. Lipiduria Nephritic syndrome: Haematuria/RBC casts Oliguria (low urinary output of less than 400ml per day) Decreased GFR Proteinuria (nowhere near as much as nephrotic syndrome) Appearance of brownish -red (“coca cola”) urine due to presence of haematuria +RBC casts
33
Types of nephrotic syndrome
Focal segmental glomerulosclerosis Membranous nephropathy Amyloidosis Minimal change disease Diabetic nephropathy
34
Types of nephritic syndrome
Post-streptococcal GN (acute) Alport syndrome IgA Nephropathy Rapidly progressive Glomerulonephritis
35
Types of mixed nephrotic/nephritic syndrome
Membranoproliferative GN Diffuse proliferative GN
36
Nephritic syndrome can also present with oedema. True/false
True, nephritic syndrome can also present with mild oedema. Whereas nephrotic syndrome will result in more apparent oedema. This is due to hypoalbuminaemia and large loss of the albumin protein in the urine.
37
Another name for IgA nephropathy?
Berger disease