Book Flashcards

1
Q

What are the causes of metabolic acidosis?

A
  • Renal disease
  • Diabetic ketoacidosis
  • Lactic acidosis caused by tissue anoxia (deprivation of oxygen) or liver disease
  • Certain cases of over dosage or poisoning
  • Chronic diarrhoea or intestinal fistula
  • Renal tubular acidosis
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2
Q

What are the clinical effects of acidosis?

A
  • Hyperventilation
  • Neuromuscular irritability
  • Hazard of arrythmias progressing to cardiac arrest (more likely in presence of hyperkalaemia)
  • Depression of consciousness which can progress to coma and death
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3
Q

What are the causes of metabolic alkalosis?

A
  • Loss of hydrogen ions in gastric fluid during vomiting
  • Potassium deficiency (often a consequence of diuretic therapy)
  • Ingestion of an absorbable alkali such as sodium bicarbonate (very large dosage required)
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4
Q

What are the clinical effects of metabolic alkalosis?

A
  • Hypoventilation
  • Confusion
  • Coma
  • Muscle cramps
  • Paraesthesia
  • Tetany
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5
Q

What are some examples of acute respiratory acidosis?

A
  • Choking
  • Bronchopneumonia
  • Acute exacerbation of asthma/chronic obstructive pulmonary disorder (COPD)
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6
Q

What are some examples of acute respiratory alkalosis?

A
  • Hysterical over-breathing
  • Mechanical over-ventilation in an intensive care patient
  • Raised intracranial pressure, or hypoxia, both of which stimulate the respiratory centre
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7
Q

What are some examples of mixed acid-base disorders commonly encountered?

A
  • Hyperventilation causes respiratory alkalosis, with prolonged nasogastric suction that causes metabolic alkalosis
  • A patient with respiratory acidosis due to COPD and diuretic-induced potassium depletion causing metabolic alkalosis
  • Salicylate poisoning in which respiratory alkalosis occurs due to stimulation of respiratory centre, together with metabolic acidosis due to the effects of the drug on metabolism
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8
Q

What is alanine aminotransferase (ALT) used to indicate?

A

Liver damage more specifically hepatocellular damage

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9
Q

What is amylase and lipase used to indicate?

A

Cell damage in acute pancreatitis

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10
Q

What is creatine kinase used to indicate?

A

Skeletal muscle damage

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11
Q

What is alkaline phosphatase (ALK) used to indicate?

A
  • Increases in cholestatic liver disease

* Marker of osteoblast activity in bone disease

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12
Q

What is gamma-glutamyl transpeptidase (GGT) used to indicate?

A

A sensitive but non-specific liver disease marker

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13
Q

What is aspartate aminotransferase (AST) used to indicate?

A
  • Hepatocellular damage
  • Muscle damage
  • Haemolysis
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14
Q

What is required to diagnose a patient with myeloma?

A

At least two of the following
• A paraprotein in serum or urine
• Plasma cell infiltration in bone marrow
• Myeloma-related end-organ damage including skeletal lesions

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15
Q

What are some cardiac specific biomarkers for a myocardial infarction?

A
  • Troponin I

* Troponin T

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16
Q

How long after the symptoms of a myocardial infarction do the troponin molecules arise?

A

Within a few hours

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17
Q

How long do troponin molecules stay elevated after symptoms of a myocardial infarction?

A

1-2 weeks

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18
Q

What can be the cause of elevated troponin molecules?

A
  • Myocardial infarction
  • Myocarditis
  • Pulmonary embolism and stroke
  • Non-cardiac conditions (severe sepsis)
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19
Q

What conditions do the liver function tests assist in differentiating?

A
  • Acute hepatocellular damage
  • Obstruction to the biliary tract
  • Chronic liver disease
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20
Q

What does a liver function test include?

A
  • Alanine aminotransferase (ALT)
  • Bilirubin
  • Alkaline phosphatase (ALK)
  • Albumin
  • Aspartate aminotransferase (AST)
  • Gamma-glutamyl transpeptidase (GGT)
  • Prothrombin time
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21
Q

Why might the levels of bilirubin in the blood rise?

A
  • Haemolysis
  • Failure of the conjugating mechanism within the hepatocyte
  • Obstruction in the biliary system
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22
Q

What are some examples of things that can block the bile duct (extrahepatic biliary obstruction)?

A
  • Gallstones
  • Pancreatic cancer
  • Lymph nodes
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23
Q

What are the most common reasons for acute liver damage?

A
  • Poisoning
  • Infection
  • Inadequate perfusion
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24
Q

What ways can acute liver damage progress?

A
  • It may resolve, as it does in most cases
  • It may progress to acute hepatic failure
  • It may lead to chronic hepatic damage
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25
Q

What are some examples of chronic liver damage?

A
  • Alcoholic liver disease
  • Chronic active hepatitis
  • Primary biliary cirrhosis
  • Non-alcoholic fatty liver disease
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26
Q

What are the most common causes of cirrhosis?

A
  • Chronic excess alcohol ingestion
  • Viral hepatitis
  • Autoimmune diseases
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27
Q

What is an unusual cause of cirrhosis?

A
  • Can develop as a child due to α1-antitrypsin deficiency
  • Can develop as a child due to Wilson’s disease
  • Can develop in adults due to haemochromatosis
  • Can follow chronic ingestion of pyrrolizidine alkaloids (found in some herbal teas)
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28
Q

What conditions can result in secondary diabetes mellitus?

A
  • Pancreatic disease
  • Endocrine disease (Cushing’s syndrome)
  • Drug therapy
  • Insulin receptor abnormalities (rarely)
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29
Q

What are micronutrients?

A
  • Minerals
  • Trace elements
  • Required in small amounts but not of limited importance
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30
Q

What biochemical tests would be requested for suspected poisoning and why?

A

• Serum urea, electrolytes, and liver function tests to assess kidney and liver function
• Blood glucose to exclude hypoglycaemia
• Blood gases to assess acid-base status
Additional tests may be required

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31
Q

How is a diagnosis of metal poisoning done?

A
  • Plasma or blood levels of the metal
  • Urinary excretion of metals
  • An associated biochemical abnormality related to the toxicity
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32
Q

Why do some patients with malignancies have renal failure?

A
  • Obstruction of the urinary tract
  • Hypercalcaemia
  • Bence-Jones proteinuria
  • Hyperuricaemia
  • Nephrotoxicity of cytotoxic drugs
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33
Q

What does a higher than normal concentration of alpha-fetoportein (AFP) mean in foetal monitoring?

A
•	Central nervous defects
o	Anencephaly
o	Spina bifida
•	Neural tube defect
•	Placental disruption
•	Liver disease
•	Foetal or maternal tumours
•	Wrong dates (usually does not increase after 32 weeks)
•	Multiple pregnancies
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34
Q

What is screened for in antenatal screening?

A
  • Foetal screening for Down syndrome and spina bifida
  • Foetal anomaly screening by ultrasonography to identify congenital heart defects, cleft lip and confirm spina bifida
  • Sickle-cell and thalassaemia
  • HIV
  • Hepatitis B
  • Syphilis
  • Rubella
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35
Q

What is some common Point of care testing (POCT) in blood?

A
  • Blood gases
  • Glucose
  • Urea and creatinine
  • Na, K and Ca
  • Bilirubin
  • Salicylate
  • Paracetamol
  • Alcohol
  • Troponin
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36
Q

What is some common Point of care testing (POCT) in urine?

A
  • Glucose
  • Ketones
  • Red cell/haemoglobin
  • Bilirubin
  • Urobilinogen
  • pH
  • Protein
  • hCG
  • Drugs of abuse
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37
Q

What does high doses of mineralocoticoids initially lead to?

A
  • Sodium retention
  • Modest expansion of the extracellular fluid (ECF) volume (not to the extent of oedema)
  • Sodium balance is then restored
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38
Q

When measuring urine osmolality and sodium, how can the results be misleading?

A

If the patient is on steroids or diuretics

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39
Q

Why would plasma appear turbid to the naked eye?

A

The patient has severe hyperlipidaemia

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40
Q

What is chronic mild hyperkalaemia (5-6 mmol/L) a relatively common finding in?

A
  • Elderly patients

* Acute or chronic kidney disease

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41
Q

What is hydrogen ion concentration usually measured in?

A

Arterial blood anticoagulated with heparin

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42
Q

What are the components that can be identified in the pathophysiology of hydrogen ion disorders (acid-base disorders)?

A
  • Generation
  • Buffering
  • Compensation
  • Correction
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43
Q

What does acidosis signify?

A

A tendency for the hydrogen ion concentration to be above the reference range

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44
Q

What does alkalosis signify?

A

A tendency for the hydrogen ion concentration to be below the refernece range

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45
Q

What is the primary abnormality in non-respiratory (metabolic) acidosis?

A
  • Either increased production or decreased excretion of hydrogen ions other than from carbon dioxide
  • Loss of bicarbonate from the body can indirectly cause acidosis
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46
Q

What is a flial segment?

A
  • When ribs are broken in two places, the chest wall that they support cannot expand during inspiration.
  • The negative intrathoracic pressure causes it to move inwards compromising ventilatory function
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47
Q

What can cause acidosis?

A
  • Retention of carbon dioxide

* Ingestion/increased production/decreased excretion of acid or loss of bicarbonate

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48
Q

What can cause alkalosis?

A
  • Hyperventilation leading to a fall in PCO2

* Increased loss of acid

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49
Q

What is Rituximab?

A

A monoclonal antibody used to treat cancer

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50
Q

How does Rituximab work?

A
  • Binds to protein CD20 on the surface of immature B cells, and marks these cells for destruction by antibody-dependent cellular cytotoxicity
  • This slows the growth of metastases
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51
Q

What are the major functions of the kidneys?

A
  • Excretion of waste
  • Maintenance of extracellular fluid (ECF) volume and composition, including acid-base balance
  • Hormone synthesis
  • Contribute to glucose supply in the fasting state through gluconeogenesis
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52
Q

What are some measurements of glomerular filtration rate?

A
  • Clearance
  • Plasma creatinine
  • Plasma urea
  • Cystatin C
  • Estimated glomerular filtration rate
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53
Q

When is estimated glomerular filtration rate not applicable?

A
  • Acute kidney disorders
  • Pregnancy
  • In condition in which there is severe muscle wasting or oedmatous states (increased creatinine levels)
  • In children
  • Increased muscle mass in athletes and body builders
  • Malnutrition and obesity
  • After a meat-rich meal
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54
Q

What is acute kidney injury (AKI) characterized by?

A
  • Rapid loss of renal function
  • Retention of urea, creatinine, hydrogen ions and other metabolic products
  • Usually but not always oliguria
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55
Q

What is teh renal functional impairment in pre-renal acute kidney injury related to?

A

A decrease in renal blood flow

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56
Q

What is the renal functional impairment in intrinsic acute kidney injury related to?

A

Intrinsic damage to the kidenys

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57
Q

What is the renal functional impairment in post-renal acute kidney injury related to?

A

Urinary tract obstruction

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58
Q

What is uraemia?

A

Urine in the blood

59
Q

What is azotaemia?

A

Refers to an increase in the blood concentration of nitrogenous compounds

60
Q

What are some conditions that lead to a decrease in the number of functioning nephrons?

A
  • Glomerulonephritis
  • Diabetes mellitus
  • Hypertension
  • Pyelonephritis
  • Renovascular disease
  • Polycystic kidneys
61
Q

What are some examples of renal diseases that affect the tubules and has “salt-losing nephritis” syndrome?

A
  • Analgesic nephropathy
  • Polycystic disease
  • Chronic pyelonephritis
62
Q

What conditions is impairment of urinary concentration a feature?

A
  • Nephrogenic diabetes insipidus
  • Group of primary tubular disorders
  • Cranial diabetes insipidus
  • Chronic kidney disease
63
Q

What conditions can impairment of urinary concentration occur with?

A
  • Hypercalcaemia
  • Hypokalaemia
  • Certain drugs (notably lithium)
64
Q

What are the most common disease processes that affect the liver?

A
  • Hepatitis (acute or chronic or both)
  • Cirrhosis
  • Tumours (primary and secondary - more frequently secondary)
65
Q

What is bilirubinuria?

A

An increase in the plasma concentration of conjugated bilirubin and is always pathological (caused by disease)

66
Q

What does prothrombin time test?

A
  • Plasma clotting activity

* Reflects the activity of vitamin K-dependent clotting factors synthesized by the liver

67
Q

What does prothrombin time indicate?

A
  • Early feature of acute liver disease

* Prolonged prothrombin time can be an indicator of vitamin K deficiency

68
Q

What can transcutaneous ultrasound examination reveal?

A
  • Gallstones
  • Dilation of the biliary system
  • Tumours
  • Characteristic hyperechoic nature of hepatic fatty infiltration
69
Q

What is an endoscopic ultrasound good for looking at?

A
  • Visualizing pancreas

* Portal vein

70
Q

What is the doppler ultrasonography used for?

A
  • Assess blood flow

* Patency of blood vessels supplying the liver

71
Q

What is elastography used to determine?

A

The degree of liver fibrosis

72
Q

In adults, what is almost always the cause of severe jaundice?

A

Conjugated hyperbilirubinaemia

73
Q

What is the colour of urine containing water-soluble conjugated bilirubin?

A

Deep orange-brown colour

74
Q

What colour is the stool of a patient with complete biliary obstruction and why?

A

Pale in colour as no bilirubin reaches the gut therefore no stercobiln is formed to make the stool a darker colour

75
Q

What is cholangography used to examine?

A

The biliary system

76
Q

What does arteriography examine?

A

The pathological circulation in hepatic tumours

77
Q

What does computed tomography (CT) and magnetic resonance imaging examine?

A

Structural abnormalities and space-occupying lesions in the hepatobiliary system

78
Q

In diagnosing chronic liver disease, histology is the gold standard, how is the tissue obtained?

A

By percutaneous biopsy

79
Q

What is chronic hepatitis defined as?

A

Hepatic inflammation persisting for more than 6 months

80
Q

What are some causes of chronic hepatitis?

A
  • Autoimmune hepatitis
  • Chronic infection with hepatitis B or C
  • Alcohol consumption
81
Q

What are the metabolic features of acute liver failure?

A
  • Severe hyponatraemia
  • Hypocalcaemia
  • Hypoglycaemia
  • Lactic acidosis often masked by respiratory alkalosis
  • Depression of brain stem which can lead to respiratory arrest
  • Metabolic alkalosis due to potassium depletion
  • Prolonged prothrombin time
  • Low plasma urea concentration
82
Q

What is cirrhosis?

A

A process in which death of liver cells with regeneration leads to fibrosis, scarring and destruction of the normal liver architecture

83
Q

What is primary biliary cirrhosis?

A

Progressive autoimmune disease characterized by destruction of intrahepatic bile ducts, typically affecting middle-aged women

84
Q

What complications can be made from decreased hepatic function and disturbances of liver architecture?

A
  • Hepatic encephalopathy
  • Bleeding from oesophageal varices
  • Ascites
  • Acute kidney injury
  • Disturbances of endocrine function
85
Q

What are the causes of death in a patient with hepatic cirrhosis?

A
  • Hepatic encephalopathy
  • Uncontrollable bleeding
  • Septicaemia
86
Q

Plasma IgA is often increased in what liver disease?

A

Alcoholic liver disease (non-specific marker)

87
Q

Plasma IgM is often increased in what liver disease?

A

Primary biliary cirrhosis (non-specific marker)

88
Q

What is ethanol a common cause of?

A
  • Hepatic steatosis (fat accumulation in the liver) due to ethanol abuse
  • Alcoholic hepatitis (life threatening condition) develops after a bout of heavy drinking in patients with a history of excessive alcohol ingestion
  • Cirrhosis (not inevitable in heavy drinkers – only 10% of heavy drinkers develop it)
89
Q

Is hepatic steatosis reversible?

A

Yes

90
Q

Non-alcoholic fatty liver disease (NAFLD) is an umbrella term for which conditions?

A

• Wide range of conditions from simple hepatic steatosis (fat deposition alone) to non-alcoholic steatohepatitis (in which inflammation is present) which can lead to cirrhosis

91
Q

What are primary tumours associated with?

A
  • Cirrhosis
  • Persistence of hepatitis B and C
  • Various carcinogens (including aflatoxins)
92
Q

What is a valuable marker for primary hepatocellular carinomas?

A
  • Plasma α-fetoprotein

* Elevated in approximately 70% of patients with primary hepatocellular carcinomas

93
Q

In what conditions is plasma α-fetoprotein elevated in?

A
  • Primary hepatocellular carcinoma
  • Acute and chronic hepatitis (elevated to a lesser extent than primary hepatocellular carcinoma)
  • Cirrhosis (elevated to a lesser extent than primary hepatocellular carcinoma)
94
Q

What are some examples of infiltrative conditions affecting the liver?

A
  • Lymphomas

* Amyloidosis

95
Q

In what liver conditions are the patients not jaundiced?

A
  • Lymphomas
  • Amyloidosis
  • Intrahepatic tumours
96
Q

What is cholestasis?

A

Obstruction to the normal flow of bile

97
Q

What can cholestasis be a feature of?

A
  • Hepatic disease (particularly cirrhosis)

* Extrahepatic disease (carcinoma of the head of the pancreas, causing obstruction of the common bile duct)

98
Q

What are the consequences of cholestasis?

A
  • Fatigue
  • Malabsorption (particularly of fat-soluble vitamins)
  • Osteoporosis (mainly in males)
99
Q

How does jaundice present in cholestasis?

A
  • May not present in the early stages

* In cholestatic jaundice the majority of the excess bilirubin is conjugated

100
Q

What conditions are there in which jaundice is caused by an inherited abnormality?

A
  • Gilbert syndrome
  • Crigler-Najjar syndrome
  • Dubin-Johnson syndrome
  • Rotor syndrome
101
Q

What is Wilson disease?

A
  • An uncommon liver disease
  • It is an inherited abnormality (autosomal recessive) of copper metabolism characterized by decreased biliary excretion of copper and decreased incorporation of copper into caeruloplasmin (a plasma protein)
102
Q

In what conditions is a decrease in caeruloplasmin seen?

A
  • Wilson disease
  • Chronic hepatitis
  • Malnutrition
103
Q

What is haemochomatosis?

A
  • An uncommon liver disease
  • It is an inherited disorder characterized by excessive iron uptake from the gut and iron deposition in the tissues, can affect many organs including the liver
104
Q

What is α1-Antitrypsin deficiency?

A
  • An uncommon liver disease
  • An inherited condition characterized either by the absence of this protein from the plasma or by the presence of an abnormal form of the protein
  • A rare cause of cirrhosis
105
Q

What is liver transplantation used to treat?

A
  • Severe liver disease

* Both acute and chronic

106
Q

After surgery of a liver transplant, what are the major complications?

A
  • Bleeding
  • Acute kidney injury (AKI)
  • Immediate non-function of the graft
  • Infection
  • Rejection
  • (Long term) The liver disease may recur in the transplanted liver
107
Q

What are gallstones composed of?

A
  • Primarily of cholesterol
  • Bilirubin
  • Calcium salts
108
Q

What can gallstones cause?

A
  • May be clinically silent
  • Biliary colic and obstruction
  • Predispose to cholecystitis
  • Predispose to pancreatitis
109
Q

What is primary sclerosing cholangiitis (PSC)?

A

It is a cholestatic liver disease characterized by inflammation and progressive fibrosis of the biliary system, leading to cirrhosis and liver failure

110
Q

What bilirubin is the cause of neonatal jaundice?

A

Unconjugated bilirubin

111
Q

What does the acidic gastric juice of the stomach contain?

A
  • Proenzyme of pepsin (pepsinogen)

* Intrinsic factor (essential for the absorption of vitamin B12

112
Q

What controls the secretion of the acidic gastric juices?

A
  • The vagus nerve

* The hormone gastrin

113
Q

What are some examples of hypersensitivity?

A
  • Allergy to grass pollens
  • Immune complex glomerulonephritis occurring after streptococcal infection
  • Chronic granulomas produced during tuberculosis or schistosomiasis
114
Q

Which IgG subclasses are generally superior at mediating effector functions such as complement activation and ADCC?

A

IgG1 and IgG3 superior to IgG2 and IgG4

115
Q

Where is monomeric IgG a major antibody found?

A
  • Serum

* Non-mucosal tissues

116
Q

What does IgG do?

A
  • Inactivates pathogens directly

* Interacts with effectors, triggering molecules such as complement (classical pathway) and Fc receptors

117
Q

Where is pentameric IgM found?

A

Serum

118
Q

What is IgM highly efficient at triggering?

A

Complement (classical pathway)

119
Q

Where are monomer and small amounts of dimeric IgA found?

A

Serum

120
Q

What pathway of the complement system does IgA trigger?

A

Lectin pathway (mannose-binding lectin)

121
Q

Where is monomeric IgE found?

A
  • Serum (very low concentrations)

* Most are bound to IgE Fc receptors on mast cells

122
Q

Where is monomeric IgD found

A

On the surface of B cells as an antigen receptor

123
Q

Where does IgA appear selectively to defend exposed external surfaces against microorganisms?

A
  • Saliva
  • Tears
  • Nasal fluids
  • Sweat
  • Colostrum
  • Milk
  • Secretions of the lung
  • Genitourinary
  • Gastrointestinal tracts
124
Q

What secretes gastrin?

A

G cells in the antrum of the stomach

125
Q

What is most peptic ulceration associated with?

A
  • Non-steroidal inflammatory drug use

* Colonization of the stomach with Helicobacter pylori

126
Q

How is H. pylori diagnosed?

A
  • Serology

* Stool antigen test

127
Q

What are the endocrine productions of the pancreas?

A
  • Insulin
  • Glucagon
  • Pancreatic polypeptides
  • Other hormones
128
Q

What is the exocrine excretion of the pancreas?

A
  • An alkaline, bicarbonate-rich fluid containing various enzymes essential for normal digestion
  • Proenzyme forms of proteases
  • Trypsin
  • Chymotrypsin
  • Carboxypeptidase
  • The lipolytic enzyme lipase
  • Colipase
  • The starch hydrolase amylase
129
Q

The secretion of pancreatic fluid is under control of which two hormones secreted by the small intestine?

A
  • Secretin

* Cholecystokinin (CCK)

130
Q

What does the secretin stimulate in the pancreas?

A

The secretion of alkaline fluid

131
Q

What does cholecystokinin (CCK) stimulate in the pancreas?

A
  • Pancreatic enzymes
  • Contraction of the gallbladder
  • Induces satiety
132
Q

What are secretin and cholecystokinin (CCK) secreted in the presence of?

A
  • Acid
  • Amino acids
  • Partly digested proteins in the duodenum
133
Q

What are the major disorders of exocrine pancreas?

A
  • Acute pancreatitis
  • Chronic pancreatitis
  • Pancreatic cancer
  • Cystic fibrosis
134
Q

What does acute pancreatitis present with?

A
  • Acute abdomen
  • Severe pain
  • Variable degrees of shock
135
Q

What are the most known causes of acute pancreatitis?

A
  • Ethanol ingestion
  • Gallstones
  • Complication of endoscopic retrograde pancreatography (ERCP)
136
Q

What are some less-common causes of acute pancreatitis?

A
  • Infection (usually viral)
  • Hypertriglyceridaemia
  • Hypercalcaemia
137
Q

What is the clinical diagnosis of acute pancreatitis?

A
  • High serum amylase or lipase activity

* Typical appearance on computed tomography (CT) scanning

138
Q

What does chronic pancreatitis present with?

A
  • Abdominal pain
  • Malabsorption
  • Impaired glucose tolerance (occasionally)
139
Q

What enzymes are used in tests of pancreatic function?

A

Pancreatic elastase and chymotrypsin activities in faeces

140
Q

Why are pancreatic elastase and chymotrypsin used in pancreatic function tests?

A
  • These are reduced in chronic pancreatitis

* Faecal elastase is widely used to distinguish between diarrhoea of pancreatic or non-pancreatic origin

141
Q

Why can pancreatic carcinoma be difficult to diagnose?

A

Presentation often occurs as a result of metastases rather than as a direct effect of the primary tumour

142
Q

What diagnostic tool is used for pancreatic carcinoma?

A

Imaging

143
Q

Where is vitamin B12 and bile salts absorbed?

A

Terminal ileum

144
Q

Where does most of the absorption of vitamin B 12 and bile salts take place?

A

The duodenum and jejunum of the small intestines