71: Urinary System-Clincal Consideration Flashcards
A hereditary disorder of basement membrane collagen- defective alpha chains.
Alport syndrome
The clinical manifestations of Alport Syndrome:
- Hematuria
- Progressive renal failure
- Neurosensory hearing loss (deaf by 25 years)
- Ocular abnormalities
- Lens, fundus are affected
Alport Syndrome causes splitting and damage of the basement membrane that leads to leakage of….. and ………. - Hematuria - Proteinuria - Pedal edema
- Eventual renal failure by 50 years
Proteins and RBCs
Goodpasture Syndrome
Autoantibody reacts with type IV collagen of glomerular & alveolar capillary basement membrane
Goodpasture Syndrome affects …….. and ……… and causes intra-alveolar hemorrhage, atrophy of the glomerulus, and epithelial crescent fills Bowman’s space.
Affects kidney and lungs
Immune mediated disease where sub-epithelial deposition of antigen-antibody complexes in the GBM and uniform thickening of GBM.
Membranous Glomerulonephritis
Membranous glomerulonephritis causes …….trigger the synthesis & liberation proteases and oxygen radical by podocytes, mesangial cells, and endothelial cells which disrupts the integrity of GBM
Membrane complexes
Membranous glomerulonephritis causes ……….. which leads to massive proteinuria, hypoalbuminemia, and anasarca (generalized body swelling)
Leaky Barriers
Recurrent painless macroscopic hematuria following viral illness (24 - 48 hours) that results in the predominant deposition of IgA and complement complexes in glomerular mesangial matrix following RTI or GI infection
IgA Nephropathy
IgA Nephropathy causes ……….. due to swelling of the renal capsule. Leukocyte infiltration and cytokine release will stimulate mesangial proliferation and hypercellularity
Flank Pain
Complement activation in IgA nephropathy leads to damage of ………………surface leading to hematuria
Glomerular filtration
Clinical Manifestations of IgA Nephropathy:
- Enlarged, hypercellular glomeruli.
- Hyperplasia of epithelium & endothelium.
- Inflammatory cells.
- Collapsed capillaries > obstruction to blood flow.
Proliferation of epithelial cells and monocytic phagocytes within Bowman’s capsule.
Rapidly progressive glomerulonephritis
Signs of Glomerulonephritis (GN):
Rapid decline in renal function
Hallmark - “ cellular crescents”
Diabetic glomerulosclerosis:
- Kimmelsteil-Wilson Lesion involves atherosclerosis of larger vessels & hyalinization of arterioles
- Deposits of hyaline material in the mesangium of the renal corpuscles
- Diffuse infiltration of glomerular tuft with eosinophic material & also focal deposits