RENAL PATHOLOGY Flashcards

1
Q

3 layers of glomerulus

A

EC
GBM
Podocytes

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2
Q

how many pyramids

A

12

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3
Q

renal lobe

A

medullary pyramid and overlying cortex

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4
Q

major compartments of glomerulus

A

Glomerular tuft

extraglomerular tuft

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5
Q

what are the four resident cell types in glomerulus

A

mesangial cells
endothelial cells
visceral epithelial cells/ podocytes - gt
parietal epithelial cells/ egt

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6
Q

Biochemical components of GBM

A
Collagen Type 4
Laminin
Polyanionic proteoglycans
Fibronectin 
Entactin
Collagen 5 7
Amyloid P
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7
Q

Function of mesangium

A

Surface receptors for angiotensin 2,vasopressin, TXA2, PGE2
Alter glomerular capillary diameter and helps in regulating plasma blood flow
Participate in the Sequestration and clearing of immune complexes since they’ve abundant lysosomes

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8
Q

Components of JGA

A

Macula densa
Afferent arterioles terminal
Efferent arteeioles proximal
Macula densa

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9
Q

Types of renal hypoplasia

A

Oligomeganeohronic

Simple

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10
Q

Types of cystic renal dysplasia

A

Multicystic dysplasia
Localized dysplasia
Dysplasia associated with lower urinary tract obstruction

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11
Q

Complications of multicystic dysplasia

A

Nephroblastoma

RCC

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12
Q

Congenital nephronomegaly is associated with which syndrome

A

Beckwith-Wideman syndrome

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13
Q

Types of ectopic kidney

A

Simple or crossed

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14
Q

Horseshoe kidney associated with which syndrome

A

Turner syndrome

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15
Q

3 categories of RPGN

A
  1. Post infectious RPGN secondary to acute poly step GN
    Systemic diseases like Goodpasture syndrome, SLE, PAN, Wegener granulomatosis, Henoch-Schonlein purpura
  2. Idiopathic RPGN
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16
Q

How GP arise

A

spontaneously or follow influenza or exposue to organic solvents or drugs such as rifampicin

17
Q

renal manifestation of Goodpasture. Nephritic or nephrotic

18
Q

which two diseases present as asymptomatic haematuria

A

thin membrane disease

IgA nephropathy

19
Q

heterezygous mutatuion of COL4A3 COL4A4

Homozygous mutation

A

TMD

Alport syndrome

20
Q

do TMD patients develop Renal failure

21
Q

cause of death in Good pasture

22
Q

distinguish between fibrillary GN and immunotactoid glomerulopathy

A

glomerular infiltration by fibrils

glomerular deposition of ig with structural organisation as microtubules

23
Q

lesions in dG

A

Glomerular lesions
Renal vascular aterio
Pyelonephritis
Tubular lesions

24
Q

what comprises the glomerular lesions in diabetic glomerulopathy

A

BM thickening
diffuse glomeruloscelois
nodular gs
exudative lesions(fibrin caps and capsular drops)

25
which of the glomerula lesions is pathognomonic
Nodular glomeruloscelorosis
26
where is Armani-Erbstein lesion found
proximal epithelial cells | Seen in diabetic glomerulonephropathy
27
is diabetic neuropathy associated with proteinuria
yeah but it's mild
28
Conditions that predispose one to RCC
Von - Hippel Lindau Syndrome Acquired cystic disease in pts on dialysis ADPKD
29
Most common RCC seen with dialysis associated cystic disease
Papillary carcinoma
30
RCC may present in 3 ways. Name them
Autosomal dominant RCC with clear cell pattern VHL Papillary RCC
31
In RCC, which percentage has Metatastis at time of diagnosis
1/3rd
32
In RCC, where does it spread to
Perinephric fat Regional lymph nodes Lungs Bones Pelvis
33
In RCC, where does it spread to
Perinephric fat Regional lymph nodes Lungs Bones Pelvis
34
Clinical triad in RCC
Loin pain Haematuria Palpable tumor
35
Angiomyolipoma is associated with which disease
Tuberous sclerosis
36
Complication of angiomyolipoma
Retroperitoneal hemorrhage