Medicine 6 Flashcards
What are some key things that you should do when examining a patient with acromegaly?
Shake the patient’s hand feeling for doughy consistency and excessive sweating
Check blood pressure
Dipstick urine for glycosuria
Visual field testing for bitemporal hemianopia
Look at tongue and teeth
Examine cardiovascular system if time
Key questions: change in ring size, change in shoe size, changes in vision, ask for old photographs
How is acromegaly investigated?
IGF-1 levels
Glucose tolerance test and measure GH levels (should be undetectable in normal people)
Imaging: lateral skull X-ray, CT, MRI
What are the treatments for acromegaly?
Transphenoidal hypophysectomy
Pituitary irradiation
Medical (octreotide 100-200 mcg every 8 hours OR lanreotide monthly)
What are some key things that you should do when examining a patient with Cushing syndrome?
Examine face and skin looking for bruising and thin skin
Check blood pressure
Urine dipstick for glycosuria
Look for proximal myopathy (squat down and stand up) and abdominal striae
What are the main causes of Cushing syndrome?
Iatrogenic (exogenous steroids) - MOST COMMON
Pituitary adenoma (next most common)
Adrenal adenoma
Ectopic ACTH (small cell lung cancer)
Outline the treatment of Paget’s disease.
May not need treatment
Simple analgesia
IV pamidronate every 3 months (mainstay)
Regular oral alendronate
What are the main differences between the CSF findings of bacterial and viral meningitis?
Viral: clear, lymphocytes, normal glucose, normal/high protein
Bacteria: cloudy, neutrophils, low glucose, high protein
Which medication reduces vasospasm in subarachnoid haemorrhage?
Nimodipine
Describe the difference in the pathogenesis of pupil-sparing and non-pupil sparing 3rd nerve palsy.
Pupil-sparing: caused by diabetes mellitus, where damage to the vasa vasorum supplying the main trunk of the 3rd nerve causes ischaemia (but sparing of surrounding parasympathetic fibres)
NON-pupil sparing: caused by space occupying lesions (e.g. posterior communicating artery aneurysm) which put pressure on the parasympathetic fibres and the main trunk causing dilatation
Which key examinations should you do in a patient with suspected MS?
Fundoscopy - check for optic neuritis
RAPD
Check for UMN signs in other parts of the body
Check for cerebellar signs (cerebellum is often affected)
What causes clonus?
Hugely increased muscle tone (i.e. UMN sign)
List some poor prognostic features of MS.
Brainstem or cerebellar disease at onset
Onset over age of 40 years
Primary progressive MS
What are the main features of neurofibromatosis type 1?
Multiple (>5) cafe au lait patches Axillary or inguinal freckling Optic glioma Lisch nodules (hamartomas on iris) Other: meningioma, phaeochromocytoma, kyphoscoliosis, renal artery stenosis
NOTE: it is autosomal dominant (Chr17)
List some causes of lower motor neurone signs.
Motor neurone disease (also causes UMN signs)
Previous polio (destroys anterior horn cells)
Guillain-Barre syndrome
Peripheral nerve lesion (e.g. trauma around fibula causing footdrop)
List some causes of upper motor neurone signs.
Stroke
Multiple sclerosis
Brain tumour
Damage to spinal cord
What is a passive shoulder shrug used for?
Loss of swing of an arm is a sign of rigidity
This may be due to Parkinson’s disease or UMN lesion
What does a positive Romberg sign suggest?
The patient is heavily dependent on vision for balance (sensory ataxia)
i.e. proprioception in the feet is impaired (peripheral neuropathy)
What is an easy way of testing L4/5 and S1/2?
L4/5 - ask the patient to stand and raise their toes off the ground (like a penguin)
What gait abnormality would you expect to see in a patient with an UMN lesion?
Drags legs
Circumducts (unilatearl) or scissors (bilateral)
What gait abnormality would you expect to see in peripheral motor neuropathy?
Foot drop (high step)