Glomerular Disease Flashcards
Common clinical presentation of glomerular disease
Protein, hemat ,nephrotic nephritic alterd serim creatine and Aki
How you differentiate the glomerular and extraglomerular hematuria
Glomerular - RBC cast, dysphormic RBC, >500mg/day protein
Extraglomerular- normal Rbc, cast absent, 500aduii
Characteristics of nephrotic syndrome
Proteinuria
Hypoalbuminia
Generalized edema
Dyslipidimea
Others
Difference between nephrotic and nephritic syndrome
Loss of protein inflammatory
Frothy urine rbc wbc main
Subnephrotic
Proteinuria
Oliguria high bp
Mechanism toprevent proteinuria, normal protein urination
Which amount indicate renal disease
Physical ,negative charge, tubular reabsorption
<80mg/day
>500mg/day
Selective and non selective proteinuria
Immune mediated( local, systemic) and non immune mediated examples
Albumin ,albumin + large other proteins
Sle and maliganacy
Idiopathic membranous nephropathy
Minimal change disease
FSGS
Most common cause for nephrotic sundrome in children
Mechanism of disease
How confirm the disease
MCD
Larger slit
EM
MCD sensitive to
Good prognosis in
Proteinuria is often (selective/ nonselective)
Steroid
Children
Selective
Common cause of nephrotic syndrome among adult
Due to defect in
Characteristics feature
How it become CKD
Primary and secondary causes
FSGS
Podocytes
Segmental sclerosis
Segment > global sclerosis with interstiatial atrophy and tubular atropy> ckd
Idiopathic
Infections,drugs hemodynamic adptations genetics
Most common cause for nephrotic syndrome in adults
Mediated disease
Deposit the Antibody
How it become CKD
Causes
What membranous proliferative GN
Characteristics features
Membranous glomerular nephropathy
Immune complex
IgG, same as Fsgs, idiopathic,secondary - malignancy,sle,infection ,drugs
Types of amyloid deposits in glomerular nephropathy And examples
Common symptoms of amyloidosis
Treatment
Al in excess immunoglobulins
AA in chronic inflammation RA
AL in genetic caises
Proteinuria , nephrotic syndrome, kidney failure
Chemotherapy , steroids ,kidney transplant
Nephritic syndrome and glomerular haematuria
Injurius agents
Injury pattern in glomerular
Immune complex , ANCA ,OTHERS( malignant htn, bacterial toxins, hereditary)
Mesangial, endocapillary, endocapillary proliferation with necrosis, crescents
Most common cause for nephritic syndrome in children
Due or
Less commonly following
In adult common among pt
Mechanism of disease
PsGN, pharyngitis or skin, pharyngitis ,
Diabetic
Antibody cross reaction
Histoligical manifestation of PSGN
All involved
Proloferation
Infiltration
When it complicated form
Symptoms
If significant rise in creatine suspect
Acute diffuse proliferative GN
All glomruli, neutrophil,crescents,
Other names for PSGN
Commenest cause for haematuria inadults
Mechanism
IgA related systemic disease and characteristics
HSP characteristics
Acute diffuse GN, post infection GN
Iga nephropathy , autoimmune ,deposition of iga on mesangium
Heamturia due to GN and purpura due to dermal small vessel vasculitis