Renal Flashcards
(41 cards)
Types of glomerulonephritis
Minimal change disease Focal segmental glomerulosclerosis Membranous GN IgA Nephropathy Goodpasture's syndrome Etc
What is nephritic syndrome?
Inflammation in the kidneys, causing haematuria, oliguria, proteinuria, fluid retention
Criteria for Nephrotic syndrome
- Peripheral oedema
- Proteinuria
- Low serum albumin
- Hypercholesterolaemia
What is the most common cause of Primary Glomerulonephritis?
IgA Nephropathy
What is the most common cause of Glomerulonephritis overall?
Membranous glomerulonephritis
At what age does Membranous glomerulonephritis peak?
Bimodal peak- 20s + 60s
What is found on histology in Membranous glomerulonephritis?
IgG and complement deposits in basement membrane
What is Polycystic Kidney Disease?
Genetic condition where kidneys develop multiple fluid-filled cysts
What is the inheritance pattern of Polycystic Kidney Disease?
There is an autosomal dominant and an autosomal recessive type
- AD more common
How is Polycystic Kidney Disease diagnosed?
Kidney USS
Genetics
Which chromosome is affected in Autosomal recessive Polycystic Kidney Disease?
Chromosome 6
Features of Autosomal recessive Polycystic Kidney Disease
Oligohydramnios in pregnancy –> underdevelopment of lungs –> respiratory depression shortly after birth
Dysmorphic features- low set ears, flat nasal bridge
End-stage renal failure before adulthood
Complications of Autosomal dominant Polycystic Kidney Disease
Chronic loin pain, hypertension, cardiovascular disease, gross haematuria, renal stones, end-stage renal failure
Features of Autosomal dominant Polycystic Kidney Disease
Extra-renal manifestations- cerebral aneurysms, prostatic/ovarian/splenic/pancreatic/hepatic cysts, cardiac valve disease (MR), colonic diverticula, aortic root dilatation
What is the mutated gene in Autosomal dominant Polycystic Kidney Disease?
PKD1/2
Management of Polycystic Kidney Disease
Tolvaptan- slow progression of cysts and disease
Genetic counselling
Avoid anti-inflammatories + anticoagulation, contact sports
Analgesia for renal colic
Antihypertensives
Dialysis/transplant
What regular monitoring is needed in Polycystic Kidney Disease?
USS, renal function, hypertension monitoring
MR angiogram- for intracranial aneurysms
General management of Glomerulonephritis
Immunosuppression
BP control- ACEi + ARB
Presentation of nephrotic syndrome
Oedema Frothy urine (proteinuria)
Complications of nephrotic syndrome
Thrombosis
Hypertension
Hyperlipidaemia
What is the most common cause of nephrotic syndrome in i) children and ii) adults?
Children- Minimal change disease
Adults- Focal segmental glomerulonephritis
What is the peak age for IgA nephropathy (Berger’s disease)?
20s
Histology findings in IgA nephropathy (Berger’s disease)
IgA deposits and glomerular mesangial proliferation
Causes of Membranous glomerulonephritis
Mostly idiopathic
Secondary to malignancy, rheumatoid disorders and drugs (NSAIDs)