glomerular disease Flashcards

1
Q

Deposition of immune complexes formed in conjunction with group A Streptococcus infection, on the glomerular membranes

A

Acute Glomerulonephritis

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2
Q

Rapid onset of hematuria and edema. Permanent renal damage seldom occurs

A

Acute Glomerulonephritis

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3
Q

Deposition of immune
complexes from system
immune disorders on the
glomerular membrane

A

Rapidly
progressive(crescentic)
glomerulonephritis

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4
Q

Rapid onset with glomerular damage and possible progression to
end-stage renal failure

A

Rapidly progressive(crescentic) glomerulonephritis

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5
Q

Attachment of cytotoxic
antibody formed during
viral respiratory infections
to glomerular and alveolar
basement membranes

A

Good pasteur’s
syndrome

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6
Q

Hemoptysis and dyspnea followed by hematuria. Possible progression to end-stage renal failure

A

Good pasteur’s syndrome

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7
Q

Antineutrophilic cytoplasmic
autoantibody binds to
neutrophils in vascular
walls producing damage to
small vessels in the lungs
and glomerulus

A

Wegener’s
Granulomatosis

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8
Q

Pulmonary symptoms
including hemoptysis
develop first followed
by renal involvement
and possible
progression to end-
stage renal failure

A

Wegener’s
Granulomatosis

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9
Q

Occurs primarily in children following viral respiratory infections; a decrease in platelets disrupts vascular integrity

A

Henoch-Schonleinpurpura

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10
Q

Initial appearance of purpura followed by blood in sputum and stools and eventual renal involvemen. Complete recovery is common, but many progress to renal failure.

A

Henoch-Schonleinpurpura

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11
Q

Deposition of IgA on the glomerular membrane
resulting from increased levels of serum IgA

A

IgA nephropathy ( Berger’s disease)

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12
Q

Recurrent macroscopichematuria
following exercise with slow progression to
chronic glomerulonephritis

A

IgA nephropathy ( Berger’s disease)

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13
Q

Thickening of the glomerular membrane
following IgG immune complex deposition
associated with systemic disorders

A

Membranous glomerulonephritis

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14
Q

Slow progression to Nephritic syndrome or possible remission

A

Membranous glomerulonephritis

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15
Q

Cellular proliferation affecting the capillary walls or the glomerular basement membrane, possibly immune mediated.

A

Membranoproliferative glomerulonephritis

“TRAM TRACKING
PATTERN OF THE
GLOMERULUS”

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16
Q

Noticeable progression to chronic glomerulonephritis to nephritis syndrome.

A

Cellular proliferation
affecting the capillary walls
or the glomerular
basement membrane,
possibly immune mediated.

17
Q

Marked decrease in renal function resulting from glomerular damage precipitated by other renal disorders

A

Chronic glomerulonephritis

18
Q

Noticeable decrease in renal function
progressing to renal failure.

A

Chronic glomerulonephritis

19
Q

Disruption of the
electrical charges that
produce the tightly fitting
podocyte barrier resulting
in massive loss of protein
and lipids

A

Nephrotic Syndrome

20
Q

Acute on set following systemic shock Gradual progression from other glomerular disorders and then to renal failure

A

Nephrotic Syndrome

21
Q

Disruption of podocytes occurring primarily in
children following allergic reactions and immunizations

A

Minimal change disease
(Lipid nephrosis)

22
Q

Frequent complete remission following corticosteroid treatmen

A

Minimal change disease
(Lipid nephrosis)

23
Q

Disruption of podocytes in certain areas of glomeruli associated with heroin and analgesic abuse and acquired immunodeficiency syndrome

A

Focal segmental
glomerulosclerosis

24
Q

May resemble nephrotic syndrome or minimal change disease.

A

Focal segmental glomerulosclerosis

25
Genetic disorder showing lamellated and thinning of glomerular basement membrane
Alport syndrome
26
Slow progression to to nephritic syndrome and end stage renal disease
Alport syndrome
27
Most common cause of ESRD Deposition of glycosylated proteins on the glomerular basement membranes caused by poorly controlled blood glucose levels
Diabetic Nephropathy (Kimmelstiel- Wilson disease)