NEPHROLOGY Flashcards
VBG in salicylate poisoning?
raised anion gap
metabolic acidosis
what is good pastures/anti glomerular basement memberane syndrome
CFs
Management
small vessel vasculitis
causes:
- pulmonary haemorrhages
- rapid glomerulonephritis
Ix; anti glomerular basement membrane antibodies against type 4 collagen
Management:
- plasma exchange (plasmaphoresis)
- Steroids
- Cyclophosphamide
Ix anti glomerular basement membrane disease
Linear IgG deposits along basement membrane
Pulmonary haemorrhages- causing raised transfer factor
what can membranoproliferative glomerulonephritis present as? (3)
- nephrotic syndrome
- haematuria
- proteinuria
3 types of membranoproliferative glomerulonephritis
Type 1= 90% cases
EMM- tram track
cause: cryoglobulinaemia, hepatitis C
type 2=
dense deposits
causes:
partial lipodystrophy factor H deficiency#
Type 3
causes: hepatitis B and C
What type of metabolic abnormality does diarrhoea most commonly cause
normal anion gap metabolic acidosis
how to calculate anion gap
(Na+ + K+) - (Cl- + HCO-3).
Post-streptococcal glomerulonephritis onset timeline
and caused by what organism
and appearance on immunofloresence
Post-streptococcal glomerulonephritis typically occurs 7-14 days following a group A beta-haemolytic Streptococcus infection
usually strep pyogenes
GRANULAR appearance
difference between IgA nephropathy and post strep GAS glomerulonephritis
post strep glomerulonephritis= 1-2 weeks and proteinuria
IgA nephropathy=1-2 days
and macroscopic haematuria
What type of metabolic abnormality does acetazolamide most commonly cause?
normal anion gap metabolic acidosis
what is cystinuria
#i heritance pattern
CFs
management
autosomal recessive
Features
recurrent renal stones
are classically yellow and crystalline, appearing semi-opaque on x-ray
Management
hydration
D-penicillamine
urinary alkalinization
what is cystinuria
inheritance pattern
CFs
management
autosomal recessive (exception to MR DS)
recurrent renal stones. defect in the membrane transport of cystine, ornithine, lysin, arginine . COLA!!!!
Features
recurrent renal stones
are classically yellow and crystalline, appearing semi-opaque on x-ray
Management
hydration
D-penicillamine
urinary alkalinization
cyanide-nitroprusside test
test for cystinuria
first choice investigation for reflux nephropathy
Micturating cystography
what type of immunogloblin responsible for graft rejection
IgG
and DR
how to distinguish between nephrogenic DI and cranial DI
administer nasal desmopressin
nephrogenic DI: no response.
cranial DI:
alport syndrome inheritance
X linked dominant
defect in type 4 collagen
CFs alport syndrome
usually young boys
microscopic haemiaturia
renal progressive failure
BIL Sensorineural hearning loss
retinal pigmentosa
what does renal biopsy and EMM show in alport syndrome;
SPLITTING OF LAMINA DENSA
X LINKED DOMINANT
WHAT IS a staghorn calculus made of
Magnesium ammonium phosphate, (also known as struvite),
congo red staining
amyloidoisis
renal complication of SLE and the 6 types
lupus nephritis
I normal kidney
II: mesangial glomerulonephritis
III: focal segmental glomerulonephritis
IV: diffuse proliferative glomerulonephritis
V: diffuse membranous
VI: sclerosing glomerulonephritis
most severe and and COMMON and dangerous type of SLE renal involvement
type 4- diffuse proliferative glomerulonephritis
mneumonic for 6 types of SLE nephritis
Normal Angels Focus on Diffusing Profits to Members of Sceciety