Nephrotic/nephritic syndromes Flashcards
Clinical consequences of glomerulonephritis
- Dependent on where the inflammation is
- Will then cause presence of protein, blood, wbc, casts in urine
- Failure of the filtration membrane –> AKI
- May or may not lead to scarring - CKD
Features of nephrotic syndrome
- Preserved renal function
- Proteinuria > 3g/day
- Spot UPCR or ACR
- > 300mg/mmol or >180mg/mmol
- decreased serum albumin normal 40
- Decreased total protein normal 65
- Oedema
Features of nephritic syndrome
- Impaired renal function (rapid or chronic)
- Proteinuria, haematuria, leucosuria
GN - presentation symptoms
- Systemic, flu like symptoms
- Rash
- Arthralgia
- Swelling
GN - Examination
- Skin
- CVS, oedema
- Chest
- Abdomen
- Urine analysis
Urine dip - nephrotic vs nephritic
Nephrotic Nephritic Blood -/+ ++ Protein +++++ ++ Leucocytes -/+ ++ Nitrites - -
GN diagnosis - blood tests
- Serum albumin, protein
- Renal function
- Autoimmune screen
GN diagnosis - analysis of a renal biopsy
- Light microscopy
- Immuno-histology
- Electron microscopy
Minimal change nephrotic syndrome - Associations
- NSAIDS
- Lithium/gold
- Allergy
- Hodgkins
What to look for on slides - minimal change nephrotic syndrome
- Epithelial foot processes
Minimal change nephrotic syndrome - presentation
- Frothy urine, oedema
- Low albumin
- Preserved function
Minimal change nephrotic syndrome - treatment
- Steroids, calcineurin inhibitors (tacrolimus)
- 50% relapse
Membranous nephrotic causes
Autoimmune disease
- Lupus, sjorgrens, Rh Arthritis, ank spond, post transplant
Infection
- Hep B, Hep C
Drugs
- Mercury, Captopril, Gold, penicillamine
- Paraneoplastic
- Idopathic
Membranous presentation
- Nephrotic syndrome
- AKI/CKD
Membranous treatment
- Underlying cause
- Steroids, CNIs, BP
Mesangial proliferative GN
Ig A deposition
- Malaria
- Typhoid
- IgA nephropathy
Presentation variable
- Haematuria
- AKI, CKD, hypertensive crisis
Diffuse proliferative GN
IgG, IgM, C3 deposition Causes - Endocarditis - Post-streptococcal GN AKI, haematuria Treat underlying infection
Focal segmental glomerulosclerosis causes
Primary - idiopathic
Secondary
Familial - reoccurs after transplantation
Virus - HIV
Drugs - heroin, pamidronate
Obesity, hypertension, atheroemboli, sickle cell anaemia
Focal segmental glomerulosclerosis treatment
Primary and familial
- Immunosuppression and BP
- Secondary underlying cause
Crescentic GN
ANCA–associated is related to small vessel vasculitis
- granulomatosis with polyangiitis (GPA), Wegener granulomatosis
- microscopic polyangitis (MPA) Churg Strauss
GBM Disease ( Goodpasteurs) Aggressive IgA nephropathy
Treatment options for proliferative crescentic GN
Strict BP control ACE inhibitors for proteinuria >1g/day Immunosuppression - steroids - cyclophosphamide - Azathioprine - mycophenolate mofetil, - Rituximab
Membranoproliferative/mesangial capillary GN
Primary
Secondary – Hep C, endocarditis, viral infections, malaria, sickle cell disease
Treatment options for non-mesangial proliferative GN
Strict BP control
ACE inhibitors for proteinuria >1g/day
Immunosuppression
- steroids
- CNI
- mycophenolate mofetil,
- Rituximab
What is glomerulonephritis
Inflammation/proliferation, immune deposits, scarring
BM, Mesangial cells, Podocytes
Infiltration of cells into, Bowmans space,