Past papers Flashcards
What scan do for bony metastases
Technetium bisphsophonate scan
Also see activity where fractures
What scan do for meabolically active metastases
FDG PET scan
Septic arthritis with gram negative intracellular diplococci
Neisseria gonorrhoea
Get primary gonorrhoea then a few weeks later get septic arthritis
Most common cause of septic monoarthritis in someone aged 19-30
Neisseria gonorrhoea
Gram negative intracellular diplococci causing meningitis
Neisseria meningitidis
6 year old with gram negative rods on lumbar puncture
Haemophilus influenzae
Neonate or premature with gram negative rods on lumbar puncture
E coli
Only causes meningitis in neonates and premature babies
Gram positive diplococci on blood culture
Step pneumoniae
Gram positive in clusters
Staph aureus
Mild fever PUO, cultures come back gram positive cocci
Strep viridans
What malignancy is lambert eaton associated with
Small cell lung cancer
Which coagulation factor decreases quickest after warfarin
VII
What does a normal osmolality with hyponatraemia suggest
Pseudohyponatraemia
Caused by hyperlipidaemia or paraproteinaemia
What is needed for a true hyponatraemia
A low osmolality
How to differentiate between causes of hypovolaemic hyponatraemia
Look at urinary sodium
- if over 20 then renal cause (drugs, salt losing nephropathy)
- if under 20 diarrhoea etc
Hypokalaemia with hypoglycaemia
Insulin OD
What causes hypokalaemia, hypotension and hypercalciuria
Bartter syndrome
Bartter syndrome (BS) is a rare inherited disease characterised by a defect in the thick ascending limb of the loop of Henle, which results in low potassium levels (hypokalemia),[2] increased blood pH (alkalosis), and normal to low blood pressure.
Closely related to Gitelmann’s
Specifically, mutations directly or indirectly involving the Na-K-2Cl cotransporter are key. The Na-K-2Cl cotransporter is involved in electroneutral transport of one sodium, one potassium, and two chloride ions across the apical membrane of the tubule. The basolateral calcium-sensing receptor has the ability to downregulate the activity of this transporter upon activation.
Hyperkalaemia with a low aldosterone
ACEi
Reduced production of aldosterone
What are the types of renal tubular acidosis and their affect on potassium handling
Type 1 (distal tubule)- hypokalaemia
Type 2 (proximal tubule)- hypokalaemia
Type 3 (both DCT and PCT)- hypokalaemia
Type 4 (adrenals) - hyperkalaemia
Highest number has hyperK+
Eg of cause of type 4= addisons
What is used to differentiate causes of metabolic acidosis
Anion gap (NR 10-18)
Brittle hair and developmental delay
Homocysteinuria
Homocystinuria is a genetic disorder that affects the metabolism of the amino acid methionine
Cherry red spot
Developmental delay
Deafness and blindness
Fabrys disease (lysosomal disease)
The genetic mutation that causes Fabry disease interferes with the function of an enzyme that processes biomolecules known as sphingolipids, leading to these substances building up in the walls of blood vessels and other organs. It is inherited in an X-linked manner.
Encephalopathy- hypotonia, lethargy, poor feeding
Sweet odour and sweaty feet
Maple syrup disease
(MSUD- Maple syrup urine disease)
The condition gets its name from the distinctive sweet odor of affected infants’ urine and earwax, particularly prior to diagnosis and during times of acute illness
How to tell difference between primary and tertiary hyperparathyroidism
Can be very difficult to tell difference biochemically however presence of CKD shows is tertiary