Glomerular Diseases
Glomerular Diseases
Microanatomy
 The nephron is the basic unit of the kidney, each
  kidney contain about one million nephron.
 The nephron consist of the glomerulus &the
  associated tubules that lead to the collecting
  duct .
 The Glomerulus : is a ball of capillaries
  surrounded by Bowman’s capsule.
 The glomerulus receive blood from afferent
  arteriole & is drained by the efferent arteriole.
nephron
the functional unit of the kidney
•capable of forming urine

•has two major components:
    glomerulus
    tubule:
        proximal
        loop of Henle
        distal
        collecting
The glomerulus contain 4 different types of
  cells:
 1- Visceral epithelial cell( podocytes ).
   these cells have long projections from
  which foot processes arise & attach to the
  glomerular basement membrane ( make
  support to the GBM ) .

2- Endothelial cells.
  these cells line the capillary lumen.
3- Mesangial cells:
  the mesangium provide a skeletal framwork to
  support the capillary loops & have contractile &
  phagocytic properties.
 due to it’s contractile capability, can control blood
  flow along the glomerular capillaries .

4-Parietal epithelial cells:
  cover Bowman’s capsule .

Glomerular Basement Membrane: prodused by
  fusion of the basement membrane of epithelial &
  endothelial cells .
Glomerular syndromes
1- Nephrotic syndrome : Massive
 proteinuria ( > 3.5 gm/24hr. ) , with variable
 edema, hypoalbuminemia, hyperlipidemia &
 hyperlipiduria .

 A- NS with “bland” sediment : mean pure NS.
 B-NS with “active” sediment : mean “mixed”
  Nephrotic/nephritic syndrome .
 Normal proteinuria <150 mg /24 hr(<0.15gm/24
  hr) .
2- Acute nephritic syndrom : Nephronal
 hematuria (RBC cast &/or dysmorphic RBCs)
 temporally associated with acute renal failure .
3- Rapidly progressive glomerulonephritis :
 Nephronal hematuria (RBC cast &/or dysmorphic
 RBCs) with renal failure developing over weeks to
 months &diffuse glomerular crescent formation .
4-Chronic glomerulonephritis : slowly
 progressive glomerular damage with proteinuria,
 hematuria & hypertension .
5-Asymptomatic urinary abnormalities :

  - Isolated proteinuria (usually <2 gm/day )

  - hematuria (with or without proteinuria ) .
Pathologic features of glomerular
disease
 Focal :mean affect some of glomeruli (but
  not all ).
 Diffuse : mean the lesion




           affect all glomeruli or >75% .
 Segmental : mean only a part of the
  glomerulus is affected by the lesion .
 Proliferative : abnormal proliferation of
Misangial :excessive production of misangial
                   materials.
Membranous :glomeruler basement is damaged
                  &thickened .
Membranoproliferative :causing both thickening
of glomerular basement membran &proliferation of
                mesangial cells .

 Crescent formation: epithelial cell proliferation
& mononuclear cell infiltration in Bowman’s space.

medicine.glumerulur dz.(dr.kawa)

  • 1.
  • 2.
    Glomerular Diseases Microanatomy  Thenephron is the basic unit of the kidney, each kidney contain about one million nephron.  The nephron consist of the glomerulus &the associated tubules that lead to the collecting duct .  The Glomerulus : is a ball of capillaries surrounded by Bowman’s capsule.  The glomerulus receive blood from afferent arteriole & is drained by the efferent arteriole.
  • 3.
    nephron the functional unitof the kidney •capable of forming urine •has two major components: glomerulus tubule: proximal loop of Henle distal collecting
  • 4.
    The glomerulus contain4 different types of cells: 1- Visceral epithelial cell( podocytes ). these cells have long projections from which foot processes arise & attach to the glomerular basement membrane ( make support to the GBM ) . 2- Endothelial cells. these cells line the capillary lumen.
  • 5.
    3- Mesangial cells: the mesangium provide a skeletal framwork to support the capillary loops & have contractile & phagocytic properties. due to it’s contractile capability, can control blood flow along the glomerular capillaries . 4-Parietal epithelial cells: cover Bowman’s capsule . Glomerular Basement Membrane: prodused by fusion of the basement membrane of epithelial & endothelial cells .
  • 6.
    Glomerular syndromes 1- Nephroticsyndrome : Massive proteinuria ( > 3.5 gm/24hr. ) , with variable edema, hypoalbuminemia, hyperlipidemia & hyperlipiduria . A- NS with “bland” sediment : mean pure NS. B-NS with “active” sediment : mean “mixed” Nephrotic/nephritic syndrome .  Normal proteinuria <150 mg /24 hr(<0.15gm/24 hr) .
  • 7.
    2- Acute nephriticsyndrom : Nephronal hematuria (RBC cast &/or dysmorphic RBCs) temporally associated with acute renal failure . 3- Rapidly progressive glomerulonephritis : Nephronal hematuria (RBC cast &/or dysmorphic RBCs) with renal failure developing over weeks to months &diffuse glomerular crescent formation . 4-Chronic glomerulonephritis : slowly progressive glomerular damage with proteinuria, hematuria & hypertension .
  • 8.
    5-Asymptomatic urinary abnormalities: - Isolated proteinuria (usually <2 gm/day ) - hematuria (with or without proteinuria ) .
  • 9.
    Pathologic features ofglomerular disease  Focal :mean affect some of glomeruli (but not all ).  Diffuse : mean the lesion affect all glomeruli or >75% .  Segmental : mean only a part of the glomerulus is affected by the lesion .  Proliferative : abnormal proliferation of
  • 10.
    Misangial :excessive productionof misangial materials. Membranous :glomeruler basement is damaged &thickened . Membranoproliferative :causing both thickening of glomerular basement membran &proliferation of mesangial cells .  Crescent formation: epithelial cell proliferation & mononuclear cell infiltration in Bowman’s space.