Lecture 55 - CKD Pathology Flashcards

1
Q

what is the difference between benign and malignant nephrosclerosis

A

Benign – modest HTN that remains stable; damage to the kidney may occur over time

Malignant (accerlated) - an acute HTN usually on top of benign HTN that leads to vascular damage

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2
Q

Benign Nephrosclerosis

Gross Path

Histology

A

Gross: small contracted kidney

Histo: Hyalinosis, Fibroelastic Hyperplasia (reduplication of the elastic lamina)

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3
Q

malignant nephrosclerosis

Gross Path (pathognomonic term)

Histology

A

Gross: Flea bitten (rupture of renal arterioles, capillaries)

Histology - Onion skinning of arteries; Fibrinoid necrosis of arterioles

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4
Q

2 causes of renal artery stenosis:

A

Atherosclerosis – acquired; due to HLD

Dysplesia: congenital,

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5
Q

Clinically associated scenarios associated with Diabetic Glomerulosclerosis:

A

Non nephrotic proteinuria –> nephrotic syndrome –> CKD

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6
Q

Pathogenesis of DM glomerulosclerosis

A

Increased Serum Glucose –> Non enzymatic glycosylation of vascular basement membrane, which leads to protein leak

Increased ECM produciton of the GBM: Diabetic Nodules

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7
Q

DM glomerulosclerosis histology

what is the pathognomonic finding

A

LM:
Capillary basement membrane thickening

Kimmelstein-Wilson Mesnagial Nodules (Pathog)

EM – Thick basement membrane

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8
Q

Clinical findings of adult PKD

Presentation

Associated findings

A

Bilateral marked enalrgemnt of the kidneys, compression of the parenchyma —> CKD

HTN, Hematuria, Renal failure in young adult

A/w berry aneurysm, mitral valve prolapse, hepatic cysts, splenic, pancreatic, pulm cysts

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9
Q

Genetics of PKD
- what genes
what chromosomes
function of these genes

A
PKD1 - Chr 16
PKD2 - Chr 4 
Autosomal dominant 
High penetrance
Function is within cell/cell matrix interactions
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10
Q

Histology of PKD

A

Early on - large aresa of useless parenchyma

Lateer - -cysts have destroyed parenchyma;

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11
Q

Amyloidosis –
common presentation in regards to kidney disease
what is the difference between AL and AA Amyloid
(AL and AA are secondary to what other conditions respectively)

A

Presentation: heavy proteinuria

AL: IG accumulation; secondary to multiple myeloma

AA: AA protein accumulation from macrophages; secondary to chronic inflammatory conditions

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12
Q

Amyloidosis – histological features

A
H&E: 
Amorophous pink
Congo red Positive
Apple Green Biferingence under polarized light 
EM: Fibrillary Material
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