63.primary glomerulopathy/nephritis Flashcards

1
Q

definition of primary glomerulopathies

A

renal inflammatory diseases due to primary damage of glomeruli by immune-mediated mechanisms

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2
Q

how are the morphological changes in the kidneys described as?

A

identical in both

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3
Q

changes in renal tissue/urine in primary glomerulopathies

A

1.renal tissue and urine are sterile
2.inflammatory process never purulent

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4
Q

definition of secondary glomerulopathies

A

glomeruli are affected during the course of other systemic or hereditary diseases e.g lupus, alports syndrome

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5
Q

classification of primary glomerulonephritis

A
  1. Acute GN
    a) Post-streptococcal
    b) Non-streptococcal
  2. Rapidly progressive GN
  3. Minimal change disease
  4. Membranous GN
  5. Membrano-proliferative GN
  6. Focal and diffuse proliferative GN
  7. Focal segmental glomerulosclerosis (FSGS) . 8.IgAnephropathy
  8. Chronic glomerulonephritis
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6
Q

classification of secondary systemic glomerular diseases

A
  1. Lupus nephritis (SLE)
  2. Diabetic nephropathy
  3. Amyloidosis
  4. Polyarteritis nodosa
  5. Wegener’s granulomatosis
  6. Goodpasture’s syndrome
  7. Henoch-Sch6nlein purpura
  8. Systemic infectious diseases (bacterial endocarditis, syphilis, leprosy; viral e.g. HBV,
    HCV, HIV;parasitic e.g. falciparum malaria,filariasis)
  9. Idiopathic mixed cryoglobulinaemia
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7
Q

classification of hereditary nephritis

A

1.alports syndrome
2.fabrys disease
3.nail-patella syndrome

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8
Q

how do we describe the extent of glomerular injury?

A

(a) Diffuse - more than 80% are affected
(b) Focal - some glomeruli are affected (<80%)
(c) Segmental - part of one glomerulus is affected
(d) Global- the entirety of one glomerulusis affected

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9
Q

which is the more frequent glomerulonephritis?

A

diffuse and global

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10
Q

describe the nephritic syndrome

A

characterized by:
1* hematuria with red blood cell (RBC)casts,
2* oliguria,
3* azotemia,
4* varying degreesofarterial hypertension
5*glomerular pathology by inflammation and proliferation

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11
Q

describe the nephrotic syndrome

A

characterized by:
1* heavy proteinuria(i.e., > 3.5 g/day),
2* hypoalbuminemia,
3* hyperlipidemia,
4* edema.

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12
Q

which glomerulonephritides show nephritic syndrome

A
  1. Acute postinfectious glomerulonephritis;
  2. Rapidly progressive glomerulonephritis;
  3. Goodpasture’s syndrome and
  4. Glomerulonephritis with vasculitis
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13
Q

which glomerulonephritides show nephrotic syndrome

A
  1. Minimal change nephrotic syndrome
  2. Focal segmental glomerulosclerosis
  3. Membranous glomerulonephritis
  4. Membranoproliferative GN
  5. IgA nephritis
  6. Focal proliferative glomerulonephritis
  7. Diffuse sclerosing glomerulonephritis
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14
Q

which are the mechnisms of immune glomerular injury

A

1.immune complex-associated injury
2.injury associated with antibody to GBM

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15
Q

factors responsible for the deposition of immune complexes within the glomerular basement membrane:

A

1.The glomeruli are vulnerable because they filter large volumes of blood
2. Small complexes pass through to the subepithelial side of the basement membrane in contrast to larger complexes which accumulate
subendothelially and in the mesangium.

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16
Q

which are the phases of glomerular injury

A

1.exudative
2.proliferative
3.sclerotic

17
Q

describe the glomerular injury due to immune complexes

A
  1. characterized by the presenceof antigen-antibody agegregates, which usually are precipitated in the glomerulus.
  2. Immune complexes may exist preformed in the circulation aor they may arise insitu.
  3. In situ formation occurs when antibodies are directed against endogenous glomerular antigens
    e.g SLE - the antigen is DNA, which has a strong affinity for collagen molecules, and binds to the basement membrane.
18
Q

describe the glomerular injury associated with antibody to GBM

A
  1. caused by antibody directed against components (antigens) that are distributed in a continuous fashion in the basement membrane.
  2. Antibody reacts with this antigen, activating the mediators of inflammation, which cause glomerular injury.
  3. It occurs in Goodpaster’s syndrome, in which the glomerulonephritis is associated with pulmonary hemorrhages
19
Q

which are the mediators of glomerular damage

A

1.complement
2.polymorphonuclear leucocytes
3.clotting factors

20
Q

in normal conditions there are no more than …A. nuclei in one glomerulus and
no more than …B. mesangial cells in one mesangial zone

A

a-150
b-2

21
Q

for diagnosis of GN we use

A

1.renal biopsy
2.light microscopy
3.immunofluorescence
4.electron microscopy

22
Q

what is glomerular hypercellularity

A

mesangial cell proliferation and leucocytic infiltration of mesangium

23
Q

what is hyalinosis

A

accumulation of homogenous, eosinophilic material that represents precipitated plasma protein
—usually associated with inreased mesangial matrix