Glomerulonephritis Flashcards

(40 cards)

1
Q

Definition of glomerulonephritis

A

Normally means inflammation of glomeruli
Generally caused by immunologic rxn

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2
Q

Major clinical manifestation of glomerular injury

A

Proteinuria
Hematuria
Decreased GFR
Sodium retention

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3
Q

2 main syndromes by which glomerulonephritis present

A

Nephrotic syndrome
Nephritic syndrome

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4
Q

What is nephrotic syndrome

A

Protein wasting secondary to diffuse glomerular damage with proteinuria >3.5g/day , Hypoalbuminemia and edema

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5
Q

What is nephritic syndrome

A

Set of clinical manifestation with hematuria and at least one the folllowing - oliguria, hypertension, high BUN, decreased GFR

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6
Q

Main causes of primary glomerulonephritis ( immune response to something )

A

Acute glomerulonephritis
Postinfectious glomerunephritis
Post streptococcus glomerulonephritis
Infectious glomerulonephritis
Membranoproliferative glomerulonephritis
Rapidly progressive glomerulonephritis
Idiopathic membranous glomerulonephritis
Immune globulin A IgA nephropathy
Chronic glomerulonephritis
Focal glomerular sclerosis

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7
Q

Types of glomerulonephritis

A

Primary - occur on its own
Secondary - occurs afeter disease like lupus, diabetes, etc

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8
Q

Main cause of secondary glomerulonephritis

A

Good pasture syndrome
Hemolytic uremic syndrome
Polyarteritis
Progressive systemic sclerosis
SLE
Wegeners granulomatosis
Thrombocytopenic purpura
Postpartum renal failures

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9
Q

Main area of glomerulus affected when presents with nephrotic syndrome

A

Podocyte

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10
Q

Type of histological classification leading to glomerulonephritis with nephrotic syndrome

A

Minimal change
Focal segmental glomerulosclerosis
Membranous nephropathy

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11
Q

Main cause of nephrotic syndrome

A

Minimal change disease
Dominant cause of idiopathic nephrotic syndrome in childhood

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12
Q

Pathogenesis of minimal change nephropathy

A

Unknown but might be due to factors causing podocyte injury

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13
Q

Risk factors minimal change

A

Atopy
Drugs NSAIDs
Hematological
Malignancies

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14
Q

Histological presentation of minimal change

A

Fusion of podocytes in electron microscopy

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15
Q

Presentation minimal change

A

Severe nephrotic syndrome

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16
Q

Management minimal change

A

High dose glucocorticoid

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17
Q

Population more at risk of focal segmental glomerulosclerosis

A

West African because carry more apolipoprotein L1 gene variant

18
Q

Histology focal segmental glomerulosclerosis

A

Segmental scar in some glomeruli so need a lot of sample to see it and not mix it with minimal change
Podocytes foot fusion when primary focal segmental glomerulosclerosis

19
Q

Is there immune deposit in focal segmental glomerulosclerosis

A

Yes in the focal scars , and are non specific

20
Q

Causes of secondary focal segmental glomerulosclerosis

A

Healing of previous local injury
HIV infection
Heroin misuse
Morbid obesity
Chronic hypertension

21
Q

Presentation of focal segmental glomerulosclerosis

A

Primary FSGS presents as idiopathic nephrotic syndrome but less responsive to treatment than minimal change, may progress to renal impairment, can recur after transplantation

Secondary FSGS presents with variable proteinuria and outcome

22
Q

Most common cause of nephrotic syndrome in Caucasian adult

A

Membranous nephropathy

23
Q

Pathogenesis Membranous nephropathy

A

Antibodies mostly autoantibodies directed at antigens expressed on podocyte surface including M type phospholipase A2 receptor 1

24
Q

Prognosis of Membranous nephropathy

A

1/3 recover spontaneously
1/3 remainin nephrotic state
1/3 progressive CKD

25
Dx due to glomerulonephritis leading to mild nephritic syndrome
IgA nephropathy Mesangiocapillary glomerulonephritis
26
Main presentation of patient with mild nephritic syndrome
Non visible hematuria Modest proteinuria Slow progressive course of renal dx
27
Main way of detection of IgA nephropathy
During routine exam
28
Type of immune deposits in IgA nephropathy
Mesangial IgA and C3
29
Variant of IgA nephropathy common in children
Henoch-schonlein purpura
30
What is Henoch-schonlein purpura
systemic vasculitis due to infectious trigger
31
Henoch-schonlein purpura tetras symptom
Petechiae task on buttock and lower leg Abdominal pain Arthralgia Renal dx with visible or non visible haematuria with or without proteinuria
32
Prognosis of Henoch-schonlein purpura
Good with spontaneous resolution
33
Second name of mesangiocapillary glomerulonephritis
membranoproliferative glomerulonephritis
34
Renal biopsy findings in membranoproliferative glomerulonephritis
Increased mesangial cells Thickening of glomerular capillary walls
35
Typical presentation of membranoproliferative glomerulonephritis
Proteinuria Haematuria
36
Two main type of membranoproliferative glomerulonephritis
Immunoglobulin deposition from deposition of circulating immune complexes or planted antigens Complement component deposited
37
Associated risk factor to immunoglobulin type of membranoproliferative glomerulonephritis
Infection Autoimmunity Monoclonal gammopathies
38
Associated risk factors in complement type of membranoproliferative glomerulonephritis
Complement gene mutation C3 nephritic factor Partial lipodystrophy
39
Diseases leading to rapidly progressive glomerulonephritis
Focal necrotising glomerulonephritis Diffuse proliferative glomerulonephritis Anti glomerular basement membrane dx
40
Characteristics of rapidly progressive glomerulonephritis
Rapid loss o renal function over days to weeks Hypertension Oedema Non visible haematuria Proteinuria