Renal Histopath Flashcards

1
Q

Triad of nephrotic syndrome

A

Proteinuria > 3g/ day Oedema (also have dys/hyperlipidaemia (liver)) Hypoalbuminaemia

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2
Q

Nephrotic syndrome oedema pattern (1)

A

Starts peri orbitally

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3
Q

Minimal change disease: epidemiology, Light micrscopy (1), Electron microscopy (1), immunofluorescence (1), response to steroids (1), Prognosis (1)

A

Most common in children - 75% rest elderly

no changes on light microscopy

Electron microscopy - loss of podycyte foot processes

IF - no deposits

Response to steroids - 90% Prognosis -<5% ESRF

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4
Q

Membranous glomerular disease: epidemiology, Light micrscopy (1), Electron microscopy (2), immunofluorescence (2), response to steroids (1), Prognosis (1)

A

Common in adults

Diffuse GBM thickening

EM - loss of podocyte foot processes, subepithelial deposits (spikey)

IF - Ig & complement in granular deposits along GBM

Poor response to steroids 40% get ESRF after 2-20 yrs

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5
Q

Focal segmental glomerulonephritis: epidemiology, Light micrscopy (3), Electron microscopy (1), immunofluorescence (2), response to steroids (1), Prognosis (1)

A

Common in afro-carribean

LM - Focal & segmental glomerular consolidation + scarring, + hyalinosis (change in tissue to less functional/lower form)

EM - loss of podocyte foot processes

IF - Ab + complement in SCARRED areas 50% respond to steroids 50% ESRF in 10 yrs can be secondary to obesity HIV nephropathy

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6
Q

What are secondary causes of nephrotic syndrome? (2)

A

Diabetes

Amyloidosis

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7
Q

Nephrotic syndrome secondary to diabetes: histology (2)

A

Diffuse GBM thickening

Mesangial matrix nodules - KIMMELSTIEL WILSON NODULES (usually asian)

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8
Q

Nephrotic syndrome secondary to amyloidosis: histology (1)

A

APPLE GREEN BIREFRINGENCE with CONGO red stain

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9
Q

Nephrotic syndrome secondary to amyloidosis: + hints in question (6)

A

May have chronic inflammation: RA

May have chronic infection: TB - causes AA protein deposition

May have Ig light chain deposition from multiple myeloma (AL protein deposition)

Clinical clues for amyloidosis - Macroglossia, HF, hepatomegaly

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10
Q

Pathology of acute tubular injury (ATI)/ ATN (4) (the most common cause for ARF)

A

Damage to tubular epithelial cells Blockage of tubules by casts Reduced flow + haemodynamic changes ARF

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11
Q

Causes of ATN (5)

A

Ischaemia - burns, septicaemia Nephrotoxins - drugs (NSAIDs, gentamicin), radiographic contrast agents, heavy metals, myoglobins

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12
Q

Histopathology of ATN (1)

A

necrosis of short segments of tubules

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13
Q

Acute pyelonephritis: most common causative pathogen (1) Presentation (8), What is seen in urine (1)

A

Bacterial infection of kidney due to ascending infection by E. coli. Presentation: fevers, chills, flank pain, renal angle tenderness, dysuria, haematuria Leukocytic casts are seen in urine

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14
Q

Chronic pyelonephritis & reflux nephropathy: what is it? Causes (3)

A

Inflammation + scarring of the parenchyma due to recurrent & persistent bacterial infection Causes: obstruction - posterior urethral valves, renal calculi Urine reflux - reflux nephropathy

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15
Q

What is acute interstitial nephritis?

A

A hypersensitivity rxn, usually to a drug (abx, NSAIDS) Usually begins days post exposure

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16
Q

Acute interstitial nephritis presentation (5)

A

Eosinophilia, haematuria, fever, skin rash, proteinuria

17
Q

Chronic interstitial nephritis/ analgesic nephropathy, cause (1) & symptoms (4)

A

Usually in elderly due to chronic use of NSAIDs symptoms (occur late in disease): haematuria, proteinuria, HTN, anaemia

18
Q

What is ARF?

A

Rapid loss of renal function manifesting as increased Urea & creatinine

19
Q

Pre-renal causes of ARF ( 3) (most common cause of ARF)

A

Renal hypo perfusion - sepsis, hypovolaemia, burns, renal artery stenosis, acute pancreatitis

20
Q

Renal causes of ARF (3)

A

ATN - most common renal cause Acute GN thrombotic microangiopathy

21
Q

Post renal causes of ARF (4)

A

Obstruction - stones, tumours, prostatic hypertrophy, retroperitoneal fibrosis

22
Q

What is CRF?

A

Progressive, irreversible loss of renal function + symptoms of uremia - itching, anorexia, fatigue & confusion if severe

23
Q

Commonest causes of CRF in UK (5) (in order)

A

Diabetes GN HTN Reflux nephropathy Polycystic kidneys

24
Q

5 Stages of CRF

A

Stage 1 - kidney damage + normal renal function (proteinuria may be there) GFR > 90 Stage 2- mildy impaired; GFR 60-89 Stage 3 - moderately impaired; GFR 30-59 Stage 4 - severely impaired; GFR 15-29 Stage 5 - renal failure

25
Inheritance of adult polycystic kidney disease (2)
Autosomal dominant 85% due to PKD1 mutation on Cr 16 - encodes polycystin1 15% due to PKD 2 mutation on Cr 4- encodes polycystin2
26
Pathological features of PKD (3)
Large multicystic kidneys with destroyed renal parenchyma Liver cysts (in PKD1) Berry aneurysms
27
Clinical features of PKD (3)
Haematuria, flank pain, UTI clin features due to cyst complications e.g. rupture/infection/ haemorrhage
28
Lupus nephritis infor card
depending on site & intensity of IC depostion clinical presentation may be: just urinary abnormalities, nephrotic syndrome, ARF, CRF
29
6 Classes of Lupus nephritis: give 1-3
1 - minimal mesangial lupus nephritis - ICs but no structural damage 2 - mesangial proliferative lupus nephritis - ICs + mild increase in mesangial cellularity 3 - focal lupus nephritis - active swelling + proliferation in less than half the glomeruli
30
Class 4-6 of lupus nephritis
Class IV - diffuse lupus nephritis - more than half glomeruli involved Class V - membranous lupus nephritis - subepithelial IC deposition Class VI - advanced sclerosing - complete sclerosis of \> 90% of the glomeruli