Approach to Kidney Disease Flashcards
Will a patient with nephritic or nephrotic syndrome outwardly appear to be more unwell?
Nephritic syndrome
Dark brown urine can represent increased levels of these three things
Bilirubin (liver disease)
Hemoglobin
Myoglobin (rhabdomyolysis)
Method to differentiate if heme in urine is from hemoglobin or myoglobin
Microscopic analysis
Three hallmark signs of nephrotic syndrome
More than 3.5 grams of protein in the urine per day
Edema
Hypoalbuminemia
A parent with congenital polycystic kidney disease where their progressively growing renal cysts replace normal kidney tissue has this % chance of passing it on to their child
50%
ADPKD - autosomal dominant polycystic kidney disease
This condition is associated with a characteristic thickening of basement membranes of the glomerulus
Membranous nephropathy
Most common cause of nephrotic syndrome in whites and the elderly
Membranous nephropathy
Dysmorphic red blood cells seen on microscopic analysis of urine suggest this condition
Damage at the level of the kidney
RBCs misshapen from passing through glomerular basement membrane
Between which ages does anti-GBM disease most commonly occur?
Men - 20 to 40
Women - 60 to 80
This IgA nephropathy variant generally occurs in children, and has a clinical tetrad of purpuric rash on thighs, arthralgias, abdominal pain, and gross hematuria (from renal failure)
HSP (Henoch-Schonlein Purpura)
This renal condition has a classic “tram tracking” appearance on biopsy, can cause nephrotic OR nephritic syndrome, low complement levels, and a strong relationship with Hep C
MPGN (Membranoproliferative Glomerulonephritis)
(tram tracking = double inner and outer membrane)
These two signs/symptoms nearly always co-present with diabetic caused nephrotic syndrome
Peripheral nephropathy
Diabetic retinopathy
Leading cause of nephrotic syndrome in adults, especially blacks
FSGS (focal segmental glomerular syndrome)
Two causal associations for minimal change disease
NSAIDs
Hodgkin’s lymphoma
Most common glomerulonephritis worldwide
IgA nephropathy
Your patient has rapidly progressing renal failure with gross hematuria and oliguria, hemoptysis, dyspnea, and pulmonary infiltrates. What do you think they have, and how would you confirm this diagnosis?
Anti-glomerular basement membrane disease
Confirm with serology that shows Anti-GBM antibodies
Does a patient who presents with hematuria, flank pain, dysuria, or urinary frequency, but no proteinuria more likely have a renal or non-renal issue?
Non-renal source
Area where edema is first seen in cases of significant pediatric proteinuria
Periorbital edema (especially in children)