Kidney Disorders Flashcards
define polycystic kidney disease (PKD)
an autosomal dominant disease characterised by cystic dilation of renal tubular epithelium
causes of PKD
PKD1 mutation (polycystin-1) on chromosome 16 (85%) PKD2 mutation (polycystin-2) on chromosome 4
risk factors of PKD
FH of PKD
FH of intracranial aneurysm
PMH of hypertension
clinical features of PKD
flank/suprapubic and lower back pain
bilateral kidney enlargement
polyuria, dysuria and urinary urgency
external manifestation features of PKD
intracranial berry aneurysm
mitral valve prolapse
colonic diverticular
extrarenal cysts
investigations of PKD
urine dip + M,C&S
bloods (FBC, U+E, CRP and lipids)
renal US
CT abdomen and pelvic
common investigation findings in PKD
proteinuria + haematuria ⬆️ urea, creatinine and cholesterol in bloods
⬇️ eGFR
bilateral cysts and kidney enlargement on imaging
medical management of PKD
vasopressin receptor antagonist (tolvaptan)
ACE inhibitor or ARB (ramipril or losartan)
paracetamol
conservative management of PKD
regular monitoring of bloods and cyst progression
avoiding contact sport
define nephrotic syndrome
a clinical syndrome characterised by a triad of:
- proteinuria (>3g/day)
- hypoalbuminaemia
- oedema
pathophysiology of nephrotic syndrome
arise secondary to increased permeability of serum protein through a damaged basement membrane in renal glomerulus
causes of nephrotic syndrome
systemic (DM, SLE)
minimal change disease
drugs (gold or penicillamine)
clinical features of nephrotic
weight gain
loss of appetite
nausea + vomiting
frothy urine
signs of nephrotic syndrome
periorbital + peripheral oedema
mild hypertension
investigations of nephrotic syndrome
bloods (FBC, U+Es, RFTs, LFTs, autoatnibodies, serum cholesterol, glucose)
urine dipstick
renal US + biopsy