Nephritic syndrome Flashcards
What are the main abnormalities seen in nephritic syndrome?
- Haematuria - micro or macro
- Proteinuria - small amount
- HTN - usually mild
- Low urine volume - <300ml/day due to reduced renal function
What is a distinguishing feature of nephritic syndrome that indicates glomerular damage?
red cell casts
(a urinary cast composed of a matrix containing red blood cells in various stages of degeneration and visibility, characteristic of glomerular disease or renal parenchymal bleeding)
What are the causes of nephritic syndrome?
- post strep GN
- IgA nephropathy
- Rapidly progressive GN:
Goodpastures or vasculitic (Wegeners, microscopic polyangiitis, Churg-strauss) - Membranoproliferative GN
- Henoch Schonlein purpura
What are the symptoms in IgA nephropathy
Asymptomatic non-visible haematuria or episodic visible haematuria WITHIN 72hrs of infection Raised BP Proteinuria <1g
How is a diagnosis of IgA nephropathy
renal biopsy where there is IgA deposition in mesangium
What is the treatment of IgA nephropathy
ACEi, ARB reduced proteinuria + protect renal function
CS + fish oil if persistent proteinuria >1g despite 3-6m of ACEi/ARB +GFR > 50
What is Henoch Schonlein Purpura
Small vessel vasculitis + systemic variant of IgA nephropathy w IgA deposits in skin/joints/guts/ kidney
What is the presentation of HSP
- purpuric rashon extensor surfaces
- flitting polyarthritis
- abdo pain (GI bleeding)
- nephritis
How is a diagnosis of HSP made
Usually clinical
+ve IF for IgA + C3 in skin
Renal biopsy is same as IgA N
What is the treatment for HSP
Same as IgAN
steroids for gut
What is post strep GN?
Strep antigens deposited in glomerulus leading to immune complex formation and inflammation
What strep infections lead to post strep GN and how long after?
throat - 2 weeks
skin - 3-6 weeks
How is a diagnosis of post strep GN made?
evidence of strep infection:
raised ASOT, anti-DNAse B, reduced C3
What is the treatment of post strep GN?
supportive + abx
What is anti-GBM disease? what is it also known as?
Goodpasture’s disease
auto-abs to type IV collagen in glomerular and alveolar BM