Set 4 Flashcards

1
Q

HNPCC

A

Hereditary nonpolyposis colorectal cancer
= Lynch syndrome
Autosomal dominant genetic condition associated with high risk of colon cancer (+ other cancers)

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2
Q

FAP

A

Familial adenomatous polyposis

Rare, inherited condition caused by defect in adenomatous polyposis coli (APC) gene

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3
Q

Tenesmus

A

Feeling of needing to evacuate bowels, with little or no stool passed

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4
Q

Pain due to blockage of bile duct by gallstone

A

Biliary colic

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5
Q

Atelectasis

A

The collapse of a lung
Reduced or absent gas exchange
Part or whole of lun affected

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6
Q

Papillodema

A

Swelling of optic nerve at back of eye
Visual disturbances, headaches, nausea
Due to build up of pressure in or around the brain

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7
Q

Dysparenuria

A

Pain in pelvis during sexual intercourse

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8
Q

Nystagmus

A

Involuntary + uncontrollable eye movement

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9
Q

Micelle vs chylomicron

A

Micelle - bile coated lipid droplets in lumen of small intestine
Chylomicron - protein coated lipid found in the absorptive cell of the small intestine, transported into the blood

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10
Q

Pancreatic protease enzyme that, once activated, is itself a catalyst for the activation of other pro-enzymes

A

Trypsin

Trypsinogen -> trypsin (activated by enterokinase)

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11
Q

Indirect inguinal hernia

Where does hernia leave abdomen?

A

Deep inguinal ring

Passes through inguinal canal

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12
Q

Sympathetic supply to the foregut structures (e.g. stomach)

A

Greater splanchnic nerve
(Visceral afferent nerves travel back to the spine along the same path as the sympathetic supply that viscera but in the opposite direction)

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13
Q

GLUT-2

A

Transporter that moves glucose out of the enterocytes across the basolateral membrane

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14
Q

GLUT-5

A

Moves fructose across the apical membrane of the enterocytes

From gut lumen into enterocyte

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15
Q

SGLT-1

A

Sodium glucose linked transporter that co-transports Na and glucose from the gut into the enterocyte

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16
Q

ALT

A

Alanine transaminase
Specific to hepatocytes
Released into plasma when hepatocytes damaged

17
Q

ALP

A

Alkaline phosphatase

Tends to rise in biliary obstruction and bone disease

18
Q

AST

A

Aspartame aminotransferase
Raised in liver damage
Also present in reasonable quantities in cardiac and skeletal muscle
Not specific to the liver

19
Q

Major artery at risk of haemorrhage if gastric ulcer erodes through posterior aspect of body of stomach

A

Splenic artery

20
Q

Part of stomach particularly prone to ulceration

A

Lesser curve of stomach

21
Q

Most common location for peptic ulceration

A

First part of duodenum

22
Q

CURB-65 score

A
Used to assess severity of pneumonia
Confusion
Urea concentration
Respiratory rate
Blood pressure
Age > 65
23
Q

Organism causing atypical community acquired pneumonia

A

Mycoplasma pneumoniae

24
Q

Examples of organisms causing community acquired pneumonia

A
Streptococcus pneumoniae 
Haemophilus influenzae 
Mycoplasma pneumoniae 
Moraxella catarrhalis
Staphylococcus aureus
25
Q

Signs of life threatening asthma

A

Exhaustion
Confusion
Hypotension
Silent chest of auscultation

26
Q

Finger tremor in life threatening asthma

A

Finger tremor is side effect of Beta 2 agonist therapy (e.g. Salbutamol)

27
Q

Criteria for diagnosis of acute severe asthma

A

Inability to complete a sentence in one breath
Heart rate > 100 bpm
Respiratory rate > 25
Peak flow 48% of previous best

28
Q

Amount of carbonic anhydrase activity in plasma

A

Little activity

Little effect of reaction of CO2 with water in plasma

29
Q

Direction of dissociation curve when temperature rises

A

Rise in temperature
Curve shifts to right
Binding less O2 (i.e. more O2 given up)

30
Q

Most common causative organism in infective endocarditis overall (acute + subacute)

A

Staphylococcus aureus
Highly virulent, high mortality rate, often IV drug users

Strep viridans - cause in 50-60% of subacute infective endocarditis cases

31
Q

Cause of hyponatraemia in SIADH

A

Excess water reabsorption in the collecting duct

ADH causes up-regulation of aquaporin channels in collecting duct, increased water resorption

32
Q

Cause of diabetes insipidus

A

Inappropriate secretion of ADH from posterior pituitary

33
Q

Hormones stored in the posterior pituitary gland

A
Oxytocin
Vasopressin (ADH = antidiuretic hormone)
34
Q

Urine specific gravity

A

Renal concentrating ability

Normal concentrating capacity: less water intake = increased specific gravity

35
Q

Dipsogenic diabetes insipidus (= primary poly dips is = psychogenic polydipsia) cause

A

A defect or damage to the hypothalamus causing malfunction of the thirst mechanism

Excessive thirst regardless of fluid status
Individual consumes large volumes of fluid, suppresses secretion of vasopressin (ADH), increases urine output

36
Q

Action of ADH

A

Vasoconstriction
Activation of V1 receptor on vascular smooth muscle to cause vasoconstriction triggering the thirst response in the hypothalamus

Produced by hypothalamus, stored in posterior pituitary