Nephrology Flashcards
Pathophysiology and renal histology of Anti-GBM disease.
Type 2 immune response of IgG against alpha 3 subunit of type 4 collagen. Linear deposits of IgG on immunoflorescence.
Pathophysiology and renal histology of Lupus Nephritis.
Type 3 immune complex formation (anti-DNA) deposition. Full house deposition in mesangium and subendothelial layer.
Pathophysiology and renal histology of ANCA Vasculitis.
Autoantibodies against neutrophil granule proteins. Pauci-immune crescentic glomerulonephritis.
Pathophysiology and renal histology of Membranous glomerulonephritis.
Type 3 immune complex deposition disease. Subepithelial dense deposits in electron microscopy and spikes on silver staining.
Pathophysiology and renal histology of IgA vasculitis.
Type 3 IgA immune complex mediated disease. Globular IgA deposits in the mesangium.
Pathophysiology and renal histology of FSGS.
Injury to podocytes through permeability factors. Segmental sclerosis seen on renal biopsy.
Contraindications to renal biopsy.
Small hyperechoic kidneys (less than 9 cm), which are generally indicative of chronic irreversible disease
Solitary native kidney
Multiple, bilateral cysts or a renal tumor
Uncorrectable bleeding diathesis
Severe hypertension, which cannot be controlled with antihypertensive medications
Hydronephrosis
Active renal or perirenal infection
Anatomic abnormalities of the kidney which may increase risk (see above)
Skin infection over the biopsy site
An uncooperative patient
Absolute contraindications to renal transplant.
Active infections.
Active malignancy.
Active substance abuse.
Reversible renal failure.
Uncontrolled psychiatric disease.
Documented active and ongoing treatment nonadherence.
significantly shortened life expectancy.
Relative contraindications to renal transplant.
Significant sun damage Significant vascular disease History of non adherence Malnutrition Oxalosis Potential for recurrent kidney disease
What is meltzers triad and what does it indicate?
Triad of palpable purpura, arthralgia and myalgia indicating cryoglobulinaemic vasculitis.
Describe Liddles Syndrome
Autosomal dominant condition of increased sodium reabsorption and potassium excretion. ClassicL triad of hypertension hypokalaemia and metabolic acidosis. Low renin and aldosterone are seen.
Alport Syndrome Summary
X linked disorder characterised by defect in alpha 5 chain of type 4 collagen.
What are the most common causes of hypokalaemic periodic paralysis?
Autosomal dominant condition resulting from mutations in sodium and calcium channels
What is a chloride responsive metabolic alkalosis? And what causes it?
Urine chloride <20
Gastric losses
CMV prophylaxis agent post high risk renal transplant?
Valganciclovir