Nephrology Flashcards
Normal urinary protein excretion
urinary Protein/Creatinine
is < 4 mg/m’/ hour or
ratio < 0.2
Heavy-range proteinuria:
Urinary Protein/Creatinine ratio > 2 or
urinary protein excretion > 40 mg/m*/hour
Define proteinuria and enumerate its causes
Proteinuria is excretion of abnormal amounts of protein in urine.
orthostatic (postural) proteinuria: Commonest cause
Glomerular: Nephrotic syndrome, glomerulonephritis…
Tubular: Acute tubular necrosis
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classification of proteinuria
a. According to the duration:
= Transient: Fever, exercise, seizures
= Persistent: as orthostatic (Postural) Proteinuria
b. According to the origin:
Glomerular: Nephrotic syndrome, glomerulonephritis…
Tubular: Acute tubular necrosis, tubular disorders as cystinosis
Etiology of Hematuria
- Glomerular
= Glomerulonephritis: APSGN is the most common cause
= Non-minimal change nephrotic syndrome (e.g., FSGS)
= IgA nephropathy
= Collage IV nephropathies:
Alport syndrome (hereditary nephritis that may be associated with deafness)
Thin basement membrane disease
= SLE
= Henoch-Schonlein purpura nephritis - Non-Glomerular
= Urinary tract infection (pyelonephritis & cystitis): the commonest cause
= Urolithiasis (Stones) and hypercalcuria
=Sickle cell nephropathy
= Exercise
= Anatomic abnormalities e.g., cystic kidney disease
= Trauma, Tumors (Wilms tumor), Bleeding disorders
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what is alport syndrome
hereditary nephritis that may be associated with deafness)
Etiology of NS
- Idiopathic (iry) NS (90%): Renal pathology may be one of these pictures:
a. Minimal change NS (MCNS)* [85%]
b. Mesangial proliferation
c. Focal segmental glomerulosclerosis (FSGS - Secondary NS (10%)
a. Collagen-Vascular diseases: SLE & Henoch-Schonlein purpura
b. Infection: Malaria, Schistosomiasis, HBV & HCV
c. Malignancy: Lymphoma
d. Drugs: Penicillamine, Gold
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Hyperlipidemia due to:
decrease Lipoprotein lipase; the main enzyme that degrades circulating triglycerides (2ry to urinary loss)
increase Hepatic synthesis of lipoproteins lipase (2ry to hypoalbuminemia)
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whcih more sex in MCNS
male to female 2:1
CP and complication of NS
C/P
1. Generalized edema:
Site of onset: Periorbital (more apparent in morning and decreases by the end of the day)
March: Then becomes generalized (LL, ascites, pleural effusion, scrotal / vulval
edema)
e Character: Pitting
2. No persistent hypertension, No hematuria
3. Nephrotic syndrome has_a relapsing nature; often triggered by upper respiratory tract infection
Complications
1.Infection (The major complication)
Predisposing Factors:
= Edema, ascites “is good medium for infection”
= Urinary loss of Immunoglobulins
= Decreased production of opsonins that facilitate phagocytosis of capsulated
bacteria> e.g. pneumococci is the commonest
= Steroid and immunosuppressive therapy
Organisms: Pneumococci and Staphylococci are the most common
Site of infection:
“ Peritonitis > acute abdominal pain Capsiulated Srganism
= Sepsis, pneumonia, cellulitis, UTI
2.Thromboembolic events:
Predisposing Factors:
= Hemoconcentration
= Hyperlipidemia
* Urinary loss of natural anticoagulants (Antithrombin III, Protein C & S)
Site:
= Deep venous thrombosis (DVT)
= Pulmonary embolism
3. Hypovolemia: Precipitated by aggressive diuresis or diarrhea
4. Other complications: Respiratory distress,