Histopathology 10: Renal Disease Flashcards
List the triad of symptoms that define Nephrotic syndrome?
- Proteinuria (>3g/24h)
- Hypoalbuminaemia
- Oedema
What is the most common cause of nephrotic syndrome in children ?
Minimal change disease
Electron microscopy shows loss of podocyte foot processes With no signs of immune deposits on immunofluorescence. This suggests ………. a cause of Nephrotic syndrome.
Minimal change disease
Microscopy shows ‘Spikey” subepithelial deposits and diffuse glomerular membrane thickening. This is most likely ………… a cause of Nephrotic syndrome with a poor prognosis.
Membranous glomerular disease
Light microscopy shows focal and segmental glomerular consolidation and scarring. The Afro-Caribbean lady is most likely suffering with ……… a cause of Nephrotic syndrome.
Focal segmental glomerulosclerosis (FSGS)
What causes Apple green birefringence with Congo red stain ?
Amyloidosis
Does multiple myeloma cause AL or AA amyloidosis ?
AL
List 2 causes of AA amyloidosis?
Arthritis
TB
(Cause by chronic inflammation)
A mnemonic for the characteristic features of Nephritic syndrome is PHAROH. List the characteristic features?
Proteinuria (less than Nephrotic syndrome) Haematuria Azootemia (high urea and creatinine) Red cell casts Oliguria Hypertension
List 3 causers of Nephrotic syndrome ?
Minimal change disease
Membranous glomerular disease
Focal segmental glomerulosclerosis (FSGS)
Post streptococcal glomerulonephitis usually occurs 1-3 weeks post throat infection with ………………. or after Impetigo. The bloods show increased ……. and decreased …….. . Immunoflouresence shows …………………………. in the ……….. and this is a cause of nephritic syndrome.
group A alpha haemolytic streptococcus (S.pyogenes) ASOT (antistreptolysin O titre) C3 Granular deposits of IgG and C3 Basement membrane
Which cause of Nephritic syndrome characteristically occurs 1-2 days after a URTI with frank haematuria?
IgA nephropathy
Which cause of Nephritic syndrome is most aggressive and presents with particularly pronounced renal failure and oliguria?
Rapidly progressive Glomerulonephritis
What is the characteristic feature of all types of rapidly progressive glomerulonephritis?
Crescents in the glomeruli
A patient has pulmonary haemorrhage and haematuria. ImmunoFluorescence shows IgG deposition in the GBM. This is most likely ……………….
Goodpasture’s syndrome
Which HLA type is associated with Goodpasteures syndrome ?
HLA-DRB1
The main pathogenesis of Goodpasteures syndrome is ………
Anti-GMB antibodies
SLE causes Rapidly progressive glomerulonephritis. Immunoflourescence shows ……… deposition on the GMB.
Granular IgG immune complex
List 2 Pauci-immune causes of Rapidly progressive glomerulonephritis?
Granulomatosis with polyangitis (Wegener’s granulomatosis)
Microscopic polyangitis
Match these
Granulomatosis with polyangitis
Microscopic Polyangitis.
p-ANCA
c-ANCA
ANA
AMA
Granulomatosis with polyangitis c-ANCA
Microscopic Polyangitis. p-ANCA
Immunoflourescence shows scanty immune complex deposition. This suggests a ………… cause off rapidly progressive glomerulonephritis
Pauci-immune (granulomatosis with polyangitis, Microscopic polyangitis)
List the triad of characteristic features of Alport syndrome?
Nephritic syndrome
Sensorineural deafness
Eye disorders (cataracts, lens dislocation)
Benign familial haematuria is caused by ………… and shows asymptomatic haematuria which has ………….. inheritance.
Thinning of GBM
Autosomal dominant
List 3 diseases that cause asymptomatic haematuria ?
Alport syndrome
IgA nephropathy
Benign familial haematuria (thin basement membrane syndrome)
