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Title: Kidney


1
Kidney
  • The kidneys are paired organs, which have the
    production of urine as their primary function

2
  • The two kidneys are bean-shaped organs located
    near the middle of the back, just below the rib
    cage to the left and right of the spine.
  • Each about the size of a fist, these organs act
    as sophisticated filters for the body.
  • They process about 200 quarts of blood a day to
    sift out about 2 quarts of waste products and
    extra water that eventually leave the body as
    urine.

3
  • Blood enters the kidneys through arteries that
    branch inside the kidneys into tiny clusters of
    looping blood vessels.
  • Each cluster is called a glomerulus, which comes
    from the Greek word meaning filter.
  • The plural form of the word is glomeruli.
  • There are approximately 1 million glomeruli, or
    filters, in each kidney.
  • The glomerulus is attached to the opening of a
    small fluid-collecting tube called a tubule.
  • Blood is filtered in the glomerulus, and extra
    water and wastes pass into the tubule and become
    urine.
  • Eventually, the urine drains from the kidneys
    into the bladder through larger tubes called
    ureters.

4
  • secondary functions concerned with homeostatic
    functions.
  • These include the regulation of electrolytes,
    acid-base balance, and blood pressure.
  • In producing urine, the kidneys excrete wastes
    such as urea and ammonium
  • The kidneys also are responsible for the
    reabsorption of glucose and amino acids.
  • Finally, the kidneys are important in the
    production of hormones including vitamin D, renin
    and erythropoietin.

5
  • Located behind the abdominal cavity in the
    retroperitoneum, the kidneys receive blood from
    the paired renal arteries, and drain into the
    paired renal veins.
  • Each kidney excretes urine into a ureter, itself
    a paired structure that empties into the urinary
    bladder.

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  • The substance, or parenchyma, of the kidney is
    divided into two major structures superficial is
    the renal cortex and deep is the renal medulla.
  • Grossly, these structures take the shape of 8 to
    18 cone-shaped renal lobes, each containing renal
    cortex surrounding a portion of medulla called a
    renal pyramid (of Malphigi).
  • Between the renal pyramids are projections of
    cortex called renal column

8
  • Renal physiology is the study of kidney
  • function,
  • while nephrology is the medical
  • specialty concerned with diseases of the
  • nephron,
  • which is the functional unit of the kidney.

9
Glomerular Diseases
  • Many diseases affect kidney function by attacking
    the glomeruli, the tiny units within the kidney
    where blood is cleaned.
  • Glomerular diseases include many conditions with
    a variety of genetic and environmental causes,
    but they fall into two major categories
  • Glomerulonephritis (gloh-MEHR-yoo-loh-nef-RY-tis)
  • Describes the inflammation of the membrane tissue
    in the kidney that serves as a filter, separating
    wastes and extra fluid from the blood.
  • Glomerulosclerosis (gloh-MEHR-yoo-loh-skleh-ROH-si
    s)
  • Describes the scarring or hardening of the tiny
    blood vessels within the kidney.
  • Although glomerulonephritis and
    glomerulosclerosis have different causes, they
    can both lead to kidney failure.

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  • Each glomerulus-and-tubule unit is called a
    nephron.
  • Each kidney is composed of about 1 million
    nephrons.
  • In healthy nephrons, the glomerular membrane that
    separates the blood vessel from the tubule allows
    waste products and extra water to pass into the
    tubule while keeping blood cells and protein in
    the bloodstream.

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  • Glomerular diseases damage the glomeruli, letting
    protein and sometimes red blood cells leak into
    the urine.
  • Sometimes a glomerular disease also interferes
    with the clearance of waste products by the
    kidney, so they begin to build up in the blood.

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  • Furthermore, loss of blood proteins like albumin
    in the urine can result in a fall in their level
    in the bloodstream.
  • In normal blood, albumin acts like a sponge,
    drawing extra fluid from the body into the
    bloodstream, where it remains until the kidneys
    remove it.
  • But when albumin leaks into the urine, the blood
    loses its capacity to absorb extra fluid from the
    body.
  • Fluid can accumulate outside the circulatory
    system in the face, hands, feet, or ankles and
    cause swelling.
  • Top

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Symptoms of glomerular disease
  • proteinuria large amounts of protein in the
    urine
  • hematuria blood in the urine
  • reduced glomerular filtration rate inefficient
    filtering of wastes from the blood
  • hypoproteinemia low blood protein
  • edema swelling in parts of the body

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  • some of these symptoms have signs, or visible
    manifestations
  • Proteinuria may cause foamy urine.
  • Blood may cause the urine to be pink or
    cola-colored.
  • Edema may be obvious in hands and ankles,
    especially at the end of the day, or around the
    eyes when awakening in the morning, for example.

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DIAGNOSIS
  • URINE ANALYSIS-
  • protein in the urine-
  • which may be referred to as nephrotic range if
    levels are very high.
  • Red blood cells in the urine
  • are a frequent finding as well, particularly in
    some forms of glomerular disease .
  • Urinalysis provides information about kidney
    damage by indicating levels of protein and red
    blood cells in the urine.

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  • Blood tests-measure the levels of waste products
    such as
  • creatinine
  • urea nitrogen
  • To determine whether the filtering capacity of
    the kidneys is impaired.
  • If these lab tests indicate kidney damage,
  • ultrasound or an x ray to see whether the shape
    or size of the kidneys is abnormal.
  • These tests are called renal imaging.

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  • But since glomerular disease causes problems at
    the cellular level.
  • kidney biopsya procedure in which a needle is
    used to extract small pieces of tissue for
    examination with different types of microscopes,
    each of which shows a different aspect of the
    tissue.
  • A biopsy may be helpful in confirming glomerular
    disease and identifying the cause.

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  • causes glomerular disease-
  • A number of different diseases can result in
    glomerular disease.
  • It may be the direct result of an infection or a
    drug toxic to the kidneys,
  • or it may result from a disease that affects the
    entire body, like diabetes or lupus.
  • Many different kinds of diseases can cause
    swelling or scarring of the nephron or
    glomerulus.
  • Sometimes glomerular disease is idiopathic,
    meaning that it occurs without an apparent
    associated disease.

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  • can overlap
  • that is, a disease might belong to two or more
    of the categories.
  • For example, diabetic nephropathy is a form of
    glomerular disease that can be placed in two
    categories
  • systemic diseases, since diabetes itself is a
    systemic disease,
  • and sclerotic diseases, because the specific
    damage done to the kidneys is associated with
    scarring.

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Proximal tubule
  • The proximal tubule is the portion of the duct
    system of the nephron leading from Bowman's
    capsule to the loop of Henle.
  • The most distinctive characteristic of the
    proximal tubule is its brush border (or "striated
    border").
  • The luminal surface of the epithelial cells of
    this segment of the nephron is covered with
    densely packed microvilli forming a border
    readily visible under the light microscope.
  • The microvilli greatly increase the luminal
    surface area of the cells, presumably
    facilitating their resorptive function.

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  • The proximal tubule as a part of the nephron can
    be divided into two sections,
  • pars convoluta
  • pars recta.
  • Differences in cell outlines exist between these
    segments, and therefore presumably in function
    too.

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  • Pars convoluta
  • The "Pars convoluta" is the initial convoluted
    portion.
  • In relation to the morphology of the kidney as a
    whole, the convoluted segments of the proximal
    tubules are confined entirely to the renal cortex.

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  • Pars recta
  • The "Pars recta" is the following straight
    (descending) portion.
  • Straight segments descend into the outer medulla.
  • Secretion
  • Many types of medications are secreted in the
    proximal tubule

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  • Substance -salt and water -salt and
    waterapproximately two-thirds.
  • organic solutes (primarily glucose and amino
    acids)-100
  • Potassium-65
  • Urea-50
  • Phasphate-80

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  • Pathophysiology in kidney disease
  • Proximal tubular epithelial cells (PTECs) have a
    pivotal role in kidney disease.
  • Malignant
  • Most renal cell carcinoma, the most common form
    of kidney cancer, arises from the convoluted
    tubules.

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  • Non-malignant
  • Acute tubular necrosis occurs when PTECs are
    directly damaged by toxins such as
  • Antibiotics (e.g. gentamicin),
  • Pigments (e.g. myoglobin and sepsis (e.g.
    mediated by lipopolysaccharide from gram negative
    bacteria).
  • Renal tubular acidosis (proximal type) (Fanconi
    syndrome) occurs when the PTECs are unable to
    properly reabsorb glomerular filtrate so that
    there is increased loss of bicarbonate, glucose,
    amino acids and phosphate.

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  • Diseases of the kidney are diverse, but
    individuals with kidney disease frequently
    display characteristic clinical features. Common
    clinical presentations include the nephritic and
    nephrotic syndromes,
  • acute kidney failure,
  • chronic kidney disease,
  • urinary tract infection, nephrolithiasis, and
    urinary tract obstruction.

32
  • Nephritic syndrome (or acute nephritic syndrome)
  • Is a collection of signs (known as a syndrome)
    associated with disorders affecting the kidneys,
    more specifically glomerular disorders.
  • It's characterized by having small pores in the
    podocytes of the glomerulus, large enough to
    permit proteins (proteinuria) and red blood cells
    (hematuria) to pass into the urine.
  • By contrast, nephrotic syndrome is characterized
    by only proteins (proteinuria) moving into the
    urine.
  • Both nephritic syndrome and nephrotic syndrome
    result in hypoalbuminemia due to protein mainly
    albumin moving from the blood to the urine.

33
  • Hematuria can be caused by bleeding anywhere in
    the urinary tract, but if the RBCs are trapped in
    urinary casts, it is more likely that the
    bleeding originated in the nephron, and Nephritic
    syndrome becomes more probable .

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  • Signs and symptoms
  • Nephritic syndrome is characterized by
  • hematuria (blood in the urine), with red blood
    cell (RBC) casts present in the urine
  • proteinuria (protein in the urine) - small
    amounts of protein are lost in the urine, but
    this is usually trivial (lt3.5 g/day)
  • hypertension (high blood pressure)- mild
  • uremia - due to retention of waste products

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  • and variable renal insufficiency, with
  • azotemia (elevated blood nitrogen)
  • oliguria (low urine output lt400 mL/day)
  • The main features are hypertension and RBC casts.
    The proteinuria in nephritic syndrome is not
    usually severe, but may occasionally be heavy
    enough to be in the range usually found in
    nephrotic syndrome.
  • Mnemonic PHAROH Proteinuria, Hematuria,
    Azotemia, RBC casts, Oliguria, Hypertension.

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  • Nephrotic syndrome (NS), also known as nephrosis,
    is defined by the presence of-
  • Nephrotic-range proteinuria,
  • Edema,
  • Hyperlipidemia.
  • Hypoalbuminemia.
  • Nephrotic-range proteinuria in adults is
    characterized by protein excretion of 3.5 g or
    more per day.

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Acute Renal Failure
  • Acute renal failure (ARF) is the rapid breakdown
    of renal (kidney) function that occurs when high
    levels of uremic toxins (waste products of the
    body's metabolism) accumulate in the blood.
  • ARF occurs when the kidneys are unable to
    excrete (discharge) the daily load of toxins in
    the urine

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  • Based on the amount of urine that is excreted
    over a 24-hour period, patients with ARF are
    separated into two groups
  • Oliguric patients who excrete less than 500
    milliliters per day (lt 16 oz/day)
  • Nonoliguric patients who excrete more than 500
    milliliters per day (gt 16 oz/day)

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  • In nonoliguric patients, the urine is of poor
    quality (i.e., contains little waste) because the
    blood is not well filtered, despite the fact that
    an adequate volume of urine is excreted.
  • Both kidneys are failing when ARF occurs.
  • One normally functioning kidney can maintain
    adequate blood filtering.

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  • Definition
  • Chronic kidney failure is a gradual loss of your
    kidneys' filtering ability, usually due to high
    blood pressure or diabetes.
  • When kidney function is seriously impaired,
    dangerous levels of fluid and waste can quickly
    accumulate in your body.
  • In the early stages of chronic kidney failure,
    you may have few signs or symptoms.
  • Many people with chronic kidney failure don't
    realize they have a problem until their kidney
    function has decreased to less than 25 percent of
    normal.

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  • The main goal of treatment of chronic kidney
    failure is to halt or delay progression of the
    disease, usually by controlling the underlying
    cause.
  • Chronic kidney failure can progress to end-stage
    kidney disease, which is fatal without artificial
    filtering (dialysis) or a kidney transplant.

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  • Symptoms
  • Signs and symptoms may include some or many of
    the following
  • High blood pressure
  • Decreased urine output or no urine output
  • Darkly colored urine
  • Anemia
  • Nausea or vomiting

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  • Loss of appetite
  • Sudden weight change
  • A general sense of discomfort and unease
    (malaise)
  • Fatigue and weakness
  • Headaches that seem unrelated to any other cause
  • Sleep problems
  • Decreased mental sharpness

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  • Definition of Pyelonephritis
  • Pyelonephritis is a serious bacterial infection
    of the kidney that can be acute or chronic.
  • It presents with dysuria (painful voiding of
    urine), abdominal pain (radiating to the back on
    the affected side)
  • and tenderness of the bladder area and the side
    of the involved kidney (costovertebral angle
    tenderness) which may be elicited by performing
    the kidney punch

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  • In many cases there are systemic symptoms in the
    form of fever, rigors (violent shivering while
    the temperature rises), headache, and vomiting.
  • In severe cases, delirium may be present.
  • Severe cases of pyelonephritis lead to sepsis, a
    systemic response to infection characterized by
    fever, a raised heart rate, rapid breathing and
    decreased blood pressure (occasionally leading to
    septic shock).

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  • Causes
  • Most cases of "community-acquired" pyelonephritis
    are due to bowel organisms that enter the urinary
    tract.
  • Common organisms are E. coli (70-80) and
    Enterococcus faecalis.
  • Hospital-acquired infections may be due to
    coliforms and enterococci, as well as other
    organisms uncommon in the community (e.g.
    Klebsiella spp., Pseudomonas aeruginosa).
  • Most cases of pyelonephritis start off as lower
    urinary tract infections, mainly cystitis and
    prostatitis.

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  • Pathology
  • Acute pyelonephritis is an exudative purulent
    localized inflammation of the renal pelvis
    (collecting system) and kidney.
  • The renal parenchyma presents in the interstitium
    abscesses (suppurative necrosis), consisting in
    purulent exudate (pus) neutrophils, fibrin, cell
    debris and central germ colonies
    (hematoxylinophils).
  • Tubules are damaged by exudate and may contain
    neutrophil casts. In the early stages, glomeruli
    and vessels are normal.

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  • . Gross pathology often reveals pathognomonic
    radiations of hemorrhage and suppuration through
    the renal pelvis to the renal cortex.
  • Chronic infections can result in fibrosis and
    scarring.
  • Xanthogranulomatous pyelonephritis is a form of
    chronic pyelonephritis associated with
    granulomatous abscess formation and severe kidney
    destruction.

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  • Diagnosis
  • The presence of nitrite and leukocytes (white
    blood cells) on a urine dipstick test in patients
    with typical symptoms are sufficient for the
    diagnosis of pyelonephritis, and are an
    indication for empirical treatment.
  • Formal diagnosis is with culture of the urine
    blood cultures may be needed if the source of the
    infection is initially doubtful.
  • If a kidney stone is suspected (e.g. on the basis
    of characteristic colicky pain, disproportionate
    amount of blood in the urine),
  • X-rays of the kidneys, ureters and bladder (KUB)
    may assist in identifying radioopaque stones.

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  • In patients with recurrent ascending urinary
    tract infections, it may be necessary to exclude
    an anatomical abnormality, such as vesicoureteral
    reflux (urine from the bladder flowing back into
    the ureter) or polycystic kidney disease.
    Investigations that are commonly used in this
    setting are ultrasound of the kidneys or voiding
    cystourethrography .

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  • Description of Pyelonephritis
  • One of the most common renal diseases, acute
    pyelonephritis is a sudden inflammation caused by
    bacteria.
  • It primarily affects the interstitial area and
    the renal pelvis or, less often, the renal
    tubules.

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  • .

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  • There may be irritative voiding symptoms (burning
    when urinating, a sense of urgency, or increased
    frequency of urination).
  • In acute infections, the symptoms develop
    rapidly, the fever noted first, followed by
    possible changes in the color of the urine, and
    then tenderness in the flank.

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  • . As the kidney becomes more inflamed, pain, loss
    of appetite, headache, and all the general
    effects of infection develop. This type of kidney
    pain differs from renal colic pain of kidney
    stones in that it is continuous and does not come
    in waves, stays in one spot, and may be worse by
    moving around .

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  • Diagnosis of Pyelonep
  • Take a medical history,
  • perform a physical exam,
  • and recommend tests including blood tests and
    blood cultures, urinalysis and urine culture, and
    possibly an ultrasound study of the kidneys

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DIALYSIS
  • Dialysis is a procedure that is performed
    routinely on persons who suffer from acute or
    chronic renal failure, or who have ESRD.
  • The process involves removing waste substances
    and fluid from the blood that are normally
    eliminated by the kidneys.
  • Dialysis may also be used for individuals who
    have been exposed to or ingested toxic substances
    to prevent renal failure from occurring.
  • There are two types of dialysis that may be
    performed, including the following

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  • peritoneal dialysis
  • hemodialysis
  • Long-term outlook for ESRD
  • People with ESRD are living longer than ever.
    Dialysis treatments (both hemodialysis and
    peritoneal dialysis), however, are not cures for
    ESRD, but will help you feel better and live
    longer. Over the years, ESRD can cause other
    problems such as bone disease, high blood
    pressure, nerve damage, and anemia (having too
    few red blood cells).

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Renal cell carcinoma
  • Renal cell carcinoma (RCC, also known as
    hypernephroma) is a kidney cancer that originates
    in the lining of the proximal convoluted tubule,
    the very small tubes in the kidney that filter
    the blood and remove waste products.
  • RCC is the most common type of kidney cancer in
    adults, responsible for approximately 80 of
    cases.

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  • It is also known to be the most lethal of all
    the genitourinary tumors.
  • Initial treatment is most commonly a radical or
    partial nephrectomy and remains the mainstay of
    curative treatment.
  • Where the tumour is confined to the renal
    parenchyma, the 5-year survival rate is 60-70,
    but this is lowered considerably where metastases
    have spread.
  • It is resistant to radiation therapy and
    chemotherapy, although some cases respond to
    immunotherapy.

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Signs and symptoms
  • The classic triad is hematuria (blood in the
    urine), flank pain and an abdominal mass. This
    triad only occurs in 10-15 of cases, and is
    generally indicative of more advanced disease.
  • Today, the majority of renal tumors are
    asymptomatic and are detected incidentally on
    imaging, usually for an unrelated cause.

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  • Classification
  • Clear cell carcinoma
  • Papillary carcinoma
  • Chromophobe renal carcinoma
  • Collecting duct carcinoma

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  • Gross examination
  • shows a yellowish,
  • multilobulated tumor
  • in the renal cortex,
  • which frequently
  • contains zones of
  • necrosis, hemorrhage
  • and scarring.

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  • Light microscopy shows tumor cells forming cords,
    papillae, tubules or nests, and are atypical,
    polygonal and large. Because these cells
    accumulate glycogen and lipids, their cytoplasm
    appear "clear", lipid-laden, the nuclei remain in
    the middle of the cells, and the cellular
    membrane is evident.

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  • Some cells may be smaller, with eosinophilic
    cytoplasm, resembling normal tubular cells. The
    stroma is reduced, but well vascularized. The
    tumor compresses the surrounding parenchyma,
    producing a pseudocapsule.
  • Secretion of vasoactive substances (e.g. renin)
    may cause arterial hypertension, and release of
    erythropoietin may cause erythrocytosis
    (increased production of red blood cells).

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  • .
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