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Published byAvis Wilcox Modified over 9 years ago
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Renal Pathology
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Introduction: 150gm: each kidney 1700 liters of blood filtered 180 L of G. filtrate 1.5 L of urine / day. Kidney is a retro-peritoneal organ Blood supply: Renal Artery & Vein One half of kidney is sufficient – reserve kidney function: Filtration, Excretion, Secretion, Hormone synthesis.
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Kidney Location:
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Kidney Anatomy:
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Renal Pathology Outline Glomerular diseases: Glomerulonephritis Tubular diseases: Acute tubular necrosis interstitial diseases: Pyelonephritis Diseases involving blood vessels: Nephrosclerosis Cystic diseases Tumors
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Clinical Syndromes: Nephritic syndrome. –Oliguria, Haematuria, Proteinuria, Oedema. Nephrotic syndrome. –Gross proteinuria, hyperlipidemia, Acute renal failure –Oliguria, loss of Kidney function - within weeks Chronic renal failure. –Over months and years - Uremia
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Introduction Functions of the kidney: –excretion of waste products –regulation of water/salt –maintenance of acid/base balance –secretion of hormones Diseases of the kidney –glomeruli –tubules –interstitium –vessels
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Azotemia: BUN, creatinine Uremia: azotemia + more problems Acute renal failure: oliguria Chronic renal failure: prolonged uremia Abnormal findings
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Hematuria Oliguria Azotemia Hypertension Nephritic syndrome Massive proteinuria Hypoalbuminemia Edema Hyperlipidemia/-uria Nephrotic syndrome
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Glomerular diseases –Nephrotic syndrome Minimal change disease Focal segmental glomerulosclerosis Membranous nephropathy –Nephritic syndrome Post-infectious GN IgA (immune) nephropathy
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Nephrotic Syndrome Massive proteinuria Hypoalbuminemia Edema Hyperlipidemia
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Adults: systemic disease (diabetes) Children: minimal change disease Characterized by loss of foot processes Good prognosis Causes
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Minimal change disease
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Normal glumerular structure
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Normal glomerulusMinimal change disease
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Focal Segmental Glomerulosclerosis Primary or secondary Some (focal) glomeruli show partial (segmental) hyalinization Unknown pathogenesis Poor prognosis
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Focal segmental glomerulosclerosis
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Membranous Glomerulonephritis Autoimmune reaction against unknown renal antigen Immune complexes Thickened GBM Subepithelial deposits
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Membranous glomerulonephritis
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Nephritic Syndrome Hematuria Oliguria, azotemia Hypertension
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Post-infectious GN, IgA nephropathy Immunologically-mediated Characterized by proliferative changes and inflammation Causes
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Post-Infectious Glomerulonephritis Child after streptococcal throat infection Immune complexes Hypercellular glomeruli Subepithelial humps
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Post-infectious glomerulonephritis
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IgA Nephropathy Common! Child with hematuria after (URI) Upper Respiratory Infection IgA in mesangium Variable prognosis
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IgA nephropathy
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Tubular and interstitial diseases –Inflammatory lesions pyelonephritis
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Pyelonephritis Invasive kidney infection Usually ascends from UTI Fever, flank pain Organisms: E. coli, Proteus
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Women, elderly Patients with catheters or mal-formations Dysuria, frequency Organisms: E. coli, Proteus Urinary Tract Infection
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Acute pyelonephritis with abscesses
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Pyelonephritis
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Cellular cast
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Chronic pyelonephritis
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Drug-Induced Interstitial Nephritis Antibiotics, NSAIDS IgE and T-cell-mediated immune reaction Fever, eosinophilia, hematuria Patient usually recovers Analgesic nephritis is different (bad)
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Drug-induced interstitial nephritis
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Acute Tubular Necrosis The most common cause of ARF! Reversible tubular injury Many causes: ischemic (shock), toxic (drugs) Most patients recover
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Acute tubular necrosis
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Benign Nephrosclerosis Found in patients with benign hypertension Hyaline thickening of arterial walls Leads to mild functional impairment Rarely fatal
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Benign nephrosclerosis
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Malignant nephrosclerosis Arises in malignant hypertension Hyperplastic vessels Ischemia of kidney Medical emergency
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5% of cases of hypertension Super-high blood pressure, encephalopathy, heart abnormalities First sign often headache, scotomas Decreased blood flow to kidney leads to increased renin, which leads to increased BP! 5y survival: 50% Malignant Hypertension
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Malignant hypertension
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Adult Polycystic Kidney Disease Autosomal dominant Huge kidneys full of cysts Usually no symptoms until 30 years Associated with brain aneurysms.
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Adult polycystic kidney disease
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Childhood Polycystic Kidney Disease Autosomal recessive Numerous small cortical cysts Associated with liver cysts Patients often die in infancy
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Childhood polycystic kidney disease
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Medullary Cystic Kidney Disease Chronic renal failure in children Complex inheritance Kidneys contracted, with many cysts Progresses to end-stage renal disease
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Tumors –Renal cell carcinoma –Bladder carcinoma
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Renal Cell Carcinoma Derived from tubular epithelium Smoking, hypertension, cadmium exposure Hematuria, abdominal mass, flank pain If metastatic, 5y survival = 5%
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Renal cell carcinoma
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Bladder Carcinoma Derived from transitional epithelium Present with painless hematuria Prognosis depends on grade and depth of invasion Overall 5y survival = 50%
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Bladder carcinoma
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