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urinary system nephrotic syndrome nephritic syndrome kidney diseases

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This document provides an introduction to the urinary system, focusing on the nephron and its structure, as well as the description and characteristics of nephrotic and nephritic syndromes, the different causes and how to diagnose them. It also details the gross and microscopic picture and prognosis. The document is helpful for students learning about kidney diseases.

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# Introduction to the Urinary System ## Definition of the nephron: - It's the microscopic structural and functional unit of the kidney. ## The nephron is composed of: - 1- The renal corpuscle consists of a tuft of capillaries called a glomerulus inside Bowman's capsule. - 2- The renal tubule; exte...

# Introduction to the Urinary System ## Definition of the nephron: - It's the microscopic structural and functional unit of the kidney. ## The nephron is composed of: - 1- The renal corpuscle consists of a tuft of capillaries called a glomerulus inside Bowman's capsule. - 2- The renal tubule; extends from Bowman's capsule ## Histology: - Endothelium: lining of tuft capillaries - Epithelium/Podocyte: lining of Bowman's capsule - In between them is a basement membrane ## The glomerulus (plural glomeruli): - Is a network of capillaries known as a tuft, located inside the Bowman's capsule. - This tuft is supported by the mesangium; supporting background of blood vessels made up of intraglomerular mesangial cells. ## Syndrome: - A set of medical signs and symptoms which are correlated with each other and often associated with a particular disease or disorder. # Nephritic Syndrome - It is a name given to a collection of different signs and symptoms that occurs as a result of inflammation in the kidney. - **Characters (signs & symptoms):** - Hematuria - Oliguria: Passing less urine - Hypertension - Uremia: Elevated blood urea & creatinine (BUN) < 3.5 - Azotemia: Elevated nitrogen-rich waste compound in the blood - Edema: Face or leg - Mild to moderate proteinuria ## Caused by: - Deposition of immune complexes from antibodies against organisms & complement fragments cause acute inflammatory response in the glomeruli. - **Example**: Type III hypersensitivity - Acute diffuse proliferative glomerulonephritis (post streptococcal or acute glomerulonephritis) (most frequent in children) - It follows the infection of the upper respiratory tract by nephritogenic strains of group A beta hemolytic streptococci ## Gross picture: - Kidneys may be slightly enlarged and pale due to edema # Nephrotic syndrome - A kidney disorder that causes your body to pass too much protein in urine caused by damage to glomeruli - **Characters**: - Heavy proteinuria (Albuminuria) - Hypo-proteinemia - Severe generalized edema - Hyperlipidemia: The main cause is increased hepatic lipogenesis secondary to hypoalbuminemia ## Caused by: - Damage to glomeruli (tuft of capillaries) - **Examples and causes**: - Glomerulonephritis: membranous, membranoproliferative and minimal change glomerulonephritis - Systemic lupus erythematosus (SLE) - Diabetes - Amyloidosis: deposition of abnormal misfolded protein - Infections; malaria, viral B and C hepatitis - Nonsteroidal anti-inflammatory Drugs ## Gross picture: - Enlarged & pale Kidneys due to edema - **Yellowish color** due to presence of lipid resorbed from the urine into the renal tubular epithelium. # Microscopic picture: - **Nephritic syndrome** - All glomeruli: are enlarged & hypercellular due to proliferation of endothelial and mesangial cells and infiltration by neutrophils & monocytes - Blood vessels: Swelling of endothelial cells and presence of inflammatory cells obstructs capillary lumen - Tubules contain red cell casts - Interstitium: Slight leucocyte infiltrate and edema - Immunofluorescence: granular fluorescence deposited at glomerular capillary walls & mesangium for IgG-IgM & C3 - Electron Microscopy: subepithelial (between epithelial cells of Bowman's capsule, & basement membrane) electron dense deposits known as subepithelial humps: finely granular, dome-shaped,, representing immune complex deposits # Prognosis: - **Children:** age 6-10: nephritic presentation after 1 - 4 weeks strep infection of pharynx - 95% recover with conservative therapy - 1-2% develop rapidly progressive glomerulonephritis - 2-3% develop chronic glomerulonephritis - **Adults:** may have atypical presentation with sudden hypertension, edema and elevated BUN (Blood Urea Nitrogen) - 60% recover - 40% develop rapidly progressive glomerulonephritis # Microscopic picture: - **Nephrotic syndrome** - Fusion (effacement) of the foot processes of the podocytes by electron microscopy - _The tubules show:_ - Hyaline degeneration of the epithelium of the tubules due to resorption of protein from the urine. - Vacuolar degeneration of the epithelium of the tubules due to resorption of lipids from the urine. - Protein casts within the tubular lumen - Interstitium show: variable edema | Normal Capillary | Minimal Change Glomerulopathy | |:--:|:--:| | [Image of normal capillary] | [Image of minimal change glomerulopathy] | ## Pathophysiology: - Injury to podocytes - Podocyte foot process effacement & detachment - Protein leaks into ultrafiltrate (urine) ## Signs/symptoms: - High proteinuria > 3.5 g/day - Hypoalbuminemia - Water & Na+ retention - Edema - Hyperlipidemia/lipiduria - Loss of Immunoglobulins & anticoagulants in urine. - Infections, thrombotic complications "Foamy urine is a sign of proteinuria" "Pitting" edema

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