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Ben Savage
 Overview
 Causes
 Investigation
 Types
◦ Non Proliferative
◦ Proliferative
◦ Chronic
 Is a renal disease characterized
by inflammation of the glomeruli, or small
blood vessels in the kidneys
 Affects both Kidneys symmetrically
 Accounts for 1/3 of patients requiring
dialysis or transplantation
 Cardinal symptoms:
 Proteinuria
 Haematuria
 Urinary Casts
 Also presents with
◦ ARF or CRF
◦ Nephrotic or Nephritic syndrome
◦ Proteinuria & HTN
 Primary
 2ry association with:
• Wegener granulomatosis and other vasculitides
• SLE
• Certain infections (e.g Streptococcus pyogenes)
• DM
• Drugs
 Investigations:
◦ Bloods including – ANCA, Anti-GBM, ANF, C3/4 etc
◦ Renal USS
◦ Blood cultures
◦ Biopsy (providing kidney is not to small)
 Diagnosis of underlying cause is crucial for
determining prognosis and therapy
 This is characterised by lack of
hypercellularity in the glomeruli.
 Usually cause Nephrotic syndrome.
◦ Minimal change
 Causes 80% of nephrotic syndrome in children, but
only 20% in adult
 Rx- Supportive care for oedema & steroids
◦ Focal Segmental Glomerulosclerosis (FSGS)
o Primary or Secondary to:
 Reflux nephropathy, Alport syndrome, HIV or heroin use.
o Presents as a nephrotic syndrome with varying degrees
of impaired renal function
o Steroids are tried but not shown to be affective
o 50% of patients with FSGS have progressive renal
failure
◦ Membranous glomerulonephritis (MGN)
o Common type of GN in adults,
o Frequently produces a mixed nephrotic and nephritic picture
o Usually idiopathic but can be secondary to:
 Cancer, infection (malaria, hepatitis), drugs, CTD (SLE)
o Prognosis is rule of 1/3
• 1/3 remit – 1/3 remain with MGN – 1/3 progress to end-
stage renal failure (ESRF)
o Treatment with corticosteroids
 Characterised by increased number of cells in
the glomerulus (hypercellular)
 Present as a Nephritic syndrome and can
lead to ESRF
◦ IgA nephropathy (Berger's disease)
 most common type of glomerulonephritis in adults
 It usually presents as macroscopic haematuria
 Often affects young males within 24-48hrs after an
upper respiratory tract or gastrointestinal infection
 ACE inhibitors are the mainstay of treatment.
 Prognosis is variable, 20% progress to ESRF
◦ Post-infectious GN
 Can occur after any infection; most common Strep
Pyogenes
 Treatment is supportive
 Generally resolves in 2–4 weeks.
◦ Rapidly progressive GN
 Can be due to any type of GN
 Poor prognosis progression to renal failure in weeks
 Medical emergency and early intervention crucial
 Treat with aggressive immunosuppression, blood
pressure treatment and control of lipids.
 Patient present with:
• chronic renal failure
• Small shrunken kidneys
• Chronic glomerulosclerosis and fibrotic changes
 Pathological process usually burnt out and
does not respond to therapy
 Accounts for 1/3 of patients requiring dialysis
or transplantation
 Multiple presentations
 Non Proliferative usually nephrotic
 Proliferative usually nephritic
 Rapidly progressive GN is a medical emergency
Any Question

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Glomerular Nephritis

  • 2.  Overview  Causes  Investigation  Types ◦ Non Proliferative ◦ Proliferative ◦ Chronic
  • 3.  Is a renal disease characterized by inflammation of the glomeruli, or small blood vessels in the kidneys  Affects both Kidneys symmetrically  Accounts for 1/3 of patients requiring dialysis or transplantation
  • 4.  Cardinal symptoms:  Proteinuria  Haematuria  Urinary Casts  Also presents with ◦ ARF or CRF ◦ Nephrotic or Nephritic syndrome ◦ Proteinuria & HTN
  • 5.  Primary  2ry association with: • Wegener granulomatosis and other vasculitides • SLE • Certain infections (e.g Streptococcus pyogenes) • DM • Drugs
  • 6.  Investigations: ◦ Bloods including – ANCA, Anti-GBM, ANF, C3/4 etc ◦ Renal USS ◦ Blood cultures ◦ Biopsy (providing kidney is not to small)  Diagnosis of underlying cause is crucial for determining prognosis and therapy
  • 7.  This is characterised by lack of hypercellularity in the glomeruli.  Usually cause Nephrotic syndrome. ◦ Minimal change  Causes 80% of nephrotic syndrome in children, but only 20% in adult  Rx- Supportive care for oedema & steroids
  • 8. ◦ Focal Segmental Glomerulosclerosis (FSGS) o Primary or Secondary to:  Reflux nephropathy, Alport syndrome, HIV or heroin use. o Presents as a nephrotic syndrome with varying degrees of impaired renal function o Steroids are tried but not shown to be affective o 50% of patients with FSGS have progressive renal failure
  • 9. ◦ Membranous glomerulonephritis (MGN) o Common type of GN in adults, o Frequently produces a mixed nephrotic and nephritic picture o Usually idiopathic but can be secondary to:  Cancer, infection (malaria, hepatitis), drugs, CTD (SLE) o Prognosis is rule of 1/3 • 1/3 remit – 1/3 remain with MGN – 1/3 progress to end- stage renal failure (ESRF) o Treatment with corticosteroids
  • 10.  Characterised by increased number of cells in the glomerulus (hypercellular)  Present as a Nephritic syndrome and can lead to ESRF
  • 11. ◦ IgA nephropathy (Berger's disease)  most common type of glomerulonephritis in adults  It usually presents as macroscopic haematuria  Often affects young males within 24-48hrs after an upper respiratory tract or gastrointestinal infection  ACE inhibitors are the mainstay of treatment.  Prognosis is variable, 20% progress to ESRF
  • 12. ◦ Post-infectious GN  Can occur after any infection; most common Strep Pyogenes  Treatment is supportive  Generally resolves in 2–4 weeks.
  • 13. ◦ Rapidly progressive GN  Can be due to any type of GN  Poor prognosis progression to renal failure in weeks  Medical emergency and early intervention crucial  Treat with aggressive immunosuppression, blood pressure treatment and control of lipids.
  • 14.  Patient present with: • chronic renal failure • Small shrunken kidneys • Chronic glomerulosclerosis and fibrotic changes  Pathological process usually burnt out and does not respond to therapy
  • 15.  Accounts for 1/3 of patients requiring dialysis or transplantation  Multiple presentations  Non Proliferative usually nephrotic  Proliferative usually nephritic  Rapidly progressive GN is a medical emergency

Notas del editor

  1. Alport syndrome  A genetic condition characterized by the progressive loss of kidney function and hearing. The prevalence of Alport syndrome is approximately 1 in 50,000 newborns Alport syndrome can also affect the eyes. As this condition progresses, the kidneys become less able to function properly and kidney failure results. Hearing loss is a common feature of Alport syndrome, but the abnormalities in the eyes seldom lead to loss of vision.