GLOMERULAR DISEASES Flashcards

1
Q

Glomerular diseases are the most common cause of

A

chronic kidney disease and dialysis-requiring

renal failure

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2
Q

The most common of these in the developed world is

A

diabetic nephropathy.

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3
Q

Most glomerular diseases are also called glomerulonephritis (GN) or inflammation of the

A

glomerulus

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4
Q

Glomerular diseases are often as the result of

A

1-autoimmune event,
2-circulating antibodies,
3-or vasculitis.

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5
Q

A few of Glomerular diseases are non-inflammatory and caused by other mechanisms, such as

A

1-hypertensive nephrosclerosis (prolonged high BP),
2-Alport syndrome (defective Type IV collagen in the glomerular basement membrane),
3-and hemolytic-uremic syndrome (microthrombi in renal small vessels).

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6
Q

GN may be classified as follows:

A

1-Primary disease without systemic illness (e.g., membranous GN, IgA nephropathy)
2-Secondary disease due to systemic illness (e.g., post-infectious GN, diabetic nephropathy, lupus nephritis)

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7
Q

Based on presentation, it may be further classified as follows:

A

1-Nephritic (sometimes called “acute GN”) with hematuria, RBC casts, edema, hypertension, and renal failure (e.g., post-infectious GN, Goodpasture syndrome)
2-Nephrotic with heavy proteinuria, hyperlipidemia, edema, and hypertension (e.g., minimal change disease, diabetic nephropathy)
3-Rapidly progressive GN: hematuria, usually nephritic, accompanied by sub-acute renal failure (over 1–2 weeks), often with crescents seen on biopsy.

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8
Q

Many glomerular diseases can be diagnosed using …………….. ……………..and …………………. ………………………….,
but the definitive diagnosis is usually made by …………… ……………., especially when there is heavy proteinuria or renal insufficiency. In these cases …………. is usually needed, since treatment varies depending on histology.

A

clinical evaluation and specific serologies,
renal biopsy
biopsy

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9
Q

Nephritic GN is characterized by

A

1-hematuria,
2-edema,
3-red cell casts,
4-hypertension.

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10
Q

The red cells often develop an abnormal shape (called “……………….”) which distinguishes them from non-glomerular hematuria due to

A
dysmorphic
1-stones, 
2-bladder cancer, 
3-infection. 
4-Small or moderate proteinuria
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11
Q

• The edema of glomerular disease may be anywhere in the body, but is usually first seen in

A

dependent areas (ankles)

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12
Q

The edema of glomerular disease is caused by

A

avid renal sodium retention, so labs show a low urine sodium, with fractional excretion of sodium <1%.

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13
Q

• With the salt and water retention, ……………….. also develops.
• Nephritic diseases show modest amounts of ……………….in the urine, with a daily total ………. grams
per 24 hrs.
• The most important distinction between nephritic and nephrotic syndrome is the ………………(in nephritic) and degree of …………….(>………… gm/24 hrs in nephrotic).

A
hypertension 
protein
2
3.5
hematuria 
proteinuria
3.5
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14
Q

In nephritic diseases the single most important test for diagnosing GN is usually

A

the renal biopsy

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15
Q

Exceptions are post-infectious GN, where no biopsy is usually done, and systemic vasculitis, where ……….or …………. biopsy is easier and less risky. Biopsy is always done if the patient
is developing subacute renal failure (rapidly progressive GN).

A

skin or lung

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16
Q

Nephritic vascular diseases are

A
1-Granulomatosis with polyangiitis
2-Eosinophilic granulomatosis with
polyangiitis
3-Henoch-Schönlein purpura (renal
lesion = IgAN)
4-Polyarteritis nodosa
5-Cryoglobulinemia
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17
Q

Granulomatosis with polyangiitis (Wegener granulomatosis) is characterized by systemic …………… that most often involves :

A

vasculitis
1-the kidney,
2-lung,
3-and upper respiratory tract such as the sinuses or middle ear.
4-It can also involve the skin (50%), eyes (50%), joints, and GI tract.

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18
Q

If a patient with chronic upper and lower respiratory illness
does not respond to antibiotics and then develops renal failure or hematuria, consider

A

Granulomatosis with polyangiitis

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19
Q

The best initial test is the

A

cytoplasmic antineutrophil cytoplasmic antibody [C–ANCA]

or antiproteinase-3 antibody.

20
Q

The most accurate test is a biopsy of the

A

1-kidney,
2-nasal septum,
3-or lung,
looking for granulomas

21
Q

Sinus biopsy, specifically the nasal septum, is less sensitive and
has more …………… …………… results.

A

false-negative

22
Q

Granulomatosis with polyangiitis Other lab abnormalities include

A
1-elevated ESR, 
2-rheumatoid factor (50%), 
3-anemia, 
4-and leukocytosis
These findings are nonspecific
23
Q

• The P-ANCA (or anti-myeloperoxidase antibody) is found at

A

much lower frequency.

24
Q

• Complement levels are

A

normal

25
Q

Treatment of Granulomatosis with polyangiitis is

A

cyclophosphamide and glucocorticoids

26
Q

Eosinophilic granulomatosis with polyangiitis (Churg-Strauss) is a ………………….. similar to granulomatosis with polyangiitis, characterized by

A
vasculitis 
1-chronic lung involvement, 
2-neuropathy, 
3-skin lesions, 
4-GI, 
5-cardiac, 
6-renal involvement.
27
Q

All forms of vasculitis are characterized by

A

1-fever,
2-weight loss,
3-generalized malaise.

28
Q

Diagnostic keys of Eosinophilic granulomatosis with polyangiitis (Churg-Strauss) include a history of

A

1-asthma,
2-eosinophilia,
3-or another atopic disease.

29
Q

Diagnosis of Eosinophilic granulomatosis with polyangiitis requires

A

elevated eosinophils; the P-ANCA is often positive but is nonspecific.

30
Q

The most accurate test is a lung biopsy showing the …………………. and ……………………

A

granulomas and eosinophils.

31
Q

Treatment is ………………………….. and …………………………

A

cyclophosphamide and glucocorticoids.

32
Q

define Polyarteritis nodosa (PAN)

A

is a systemic vasculitis of small- and medium-sized arteries that affects virtually every organ in the body except the lung.

33
Q

Renal involvement is common and manifests as

A

1-hypertension,
2-renal insufficiency,
3-and hemorrhage due to microaneurysms.

34
Q

Like all vasculitis, PAN is associated with

A

1-fever,
2-weight loss,
3-and malaise.

35
Q

Other organs involved include
Abdominal pain and joint pain may be prominent. The abdominal pain may mimic …………….. ……………….., and the pain will occur with eating.
Anemia and an elevated sedimentation rate are present but
are too nonspecific to be useful.

A
1-skin, 
2-eyes, 
3-muscles, 
4-GI tract, 
5-heart, 
6-kidneys, 
7-and neurologic system
mesenteric ischemia
36
Q

A diagnostic key for PAN is

A

multiorgan vasculitis, sparing the lungs

37
Q

The most accurate diagnostic test is ……………. of an affected area, with sural ………….. …………. being particularly high yield especially if there are neurologic symptoms.

A

biopsy

nerve biopsy

38
Q

If there is abdominal pain, an ………………… of the involved vessels in the GI tract may eliminate the need for a biopsy.

A

angiogram

39
Q

PAN
• ……………… is seen in 10–30% of patients.
• ……………… is seen in only a minority of patients.

A

Hepatitis B

P-ANCA

40
Q

Treatment is ………………………….. and …………………………

A

glucocorticoids and cyclophosphamide

41
Q

Renal disease from cryoglobulinemia shows the lesion of ……………………………….. and is associated with ……………………………….., and less commonly …………………… The presentation may be nephritic and/or nephrotic.

A

membranoproliferative GN (type 1)
chronic hepatitis C
hepatitis B

42
Q

cryoglobulinemia is associated

A

1-joint pain,
2-neuropathy,
3-purpuric skin lesions
4-elevated ESR and low levels of complement

43
Q

Keys to diagnosis are

A

hepatitis C and positive

serum cryoglobulins

44
Q

Treatment is for the underlying

A

chronic hepatitis

45
Q

For severe disease (renal failure, heavy proteinuria), pulse doses of ………………….. and ……………………………. may help

A

steroids and plasmapheresis