Conditions Flashcards
You want to visual the bone structure of the skull, do you use a CT or MRI?
CT it has better bone visual than MRI but not good for soft tissue
You’re doing an MRI and want to visualise a potential occlusion of a cerebral artery. Which mode would you use? T1 or T2?
T1- good for fat and 4M’s methemoglobin ( haematoma), mineral deposition (Ca, mg, mn), melanin, musch (proteinaceous fluid)
T2 is more for looking for fluid likein oedema
Patient has an acoustic schwannoma. What classic picture will be obesrved on their CT?
Ice cream cone from internal acoustic meatus
Patient presents with a blown pupil what is the a likely pathology ?
Uncal transtentorial herniation that causes 3rd cranial nerve palsy
Patient has been diagnosed with a grade 1 astrocytoma. What is the prognosis of this?
Benign and also known as pilocytic. With resection full recovery
Patient has been diagnosed with a grade 2 astrocytoma. What is the prognosis of this?
NOT benign, gets worse with time, treat with surgery and radiotherpaoy and chemo. This is likely to recur. And carries a poorer prognosis if >50yrs. With added radio and chemo there is increased progression free survivial
Patient has been diagnosed with a grade 3/4 astrocytoma. What is the prognosis of this?
This is malignant and regardless of treatment there will be death within 14months.
If want to get to 14months then need radio and TMZ is an oral chemo that increases survival by 2 months
You suspect a brain tumour and do bloods to look for specific proteins that would indicate this. What are these?
AFP
HCG
LDH
Man presents with painful headache that woke them up that gets worse with coughing, difficulty walking, and slurred speech. On examination they have nystagmus, hyptonia, inability to supinate/pronate his hands and tap them together quickly. What is the likely diagnosis
Tumour of the brain
Patient has undergone neurosurgery to remove a tumour. There has been associated seizures with his tumour. What must you advise him post surgery?
He CANNOT DRIVE for 1 year and must inform the DVLA
Women with a previous breast cancer presents with seizures and headaches. You suspect a brain tumour. Which type is most common in this group of people?
Meningiomas
Patient presents with rotatory nystagmus, lack of ability to upgaze, you ask him to follow your finger and when you bring it closer for accomodation the patients eyes bulge out at you. What is his likely diagnosis
Pineal tumour
Patient presents with cafe au lait patches, axillary freckling, and fleshy nodules of the skin. He on examination has tachycardia, sweating and headaches. What is the likely diagnosis?
Neurofibromatosis type 1 with complication of phaeochromocytoma
What is the genetic makeup of duchenne muscular dystrophy?
X-linked recessive with a mutation in the protein for dystrophin
Young boy of 4 years presents as he was unable to walk until 18months and is now toe walking, and when asking him to get up from sitting he has to walk up his hands. What is the likely diagnosis?
Duchenne muscular dystrophy
What are the investigations for a patient with potential duchenne muscular dystrophy?
Bloods for CK
Electromyography, molecular genetic testing
Muscle biopsy
What are the odds of a brother of duchenne muscular dystrophy to develop the condition?
50%
What is the genetic defect that causes Huntington’s disease?
It is an autosomal dominant trait causing repeating code of CAG (which codes for glutamine)
What is the age group that is likely to develop huntingtons dease
30-50yrs
35 year old presents with a low mood and has been finding he’s become more irritated with things. It has lasted the past few months, now he also has been experiencing some uncontrolled movements of his arms and legs that some of his friends have referred to as dancing. What is thelikely diagnosis?
Huntingtons disease
What is the treatment for huntington disease?
There is no treatment it is progressive until death
What is the inheritance pattern of spinal muscular atrophy?
Autosomal recessive
What is the pathology behind spinal muscular atrophy
Progressive loss of anterior horn cells in the spinal cord and brainstem nuclei due to mutation in the SMN1 gene on chromosome 5
Mutation of what gene makes it more likely to develop alzheimers disease?
Apolipoprotein E people with this mtuation have a 55% chance of developing this condition by the time they are 80
What epidemiological group is most likely to develop alzheimers
Downsyndrome
What epidemiological group is likely to get a streptococcus pneumoniae infection leading to pyogenic meningitis?
Hospitalised patients CSF skull fructures Diabetics Alcoholics Asplenic Cochlear implants
What bug that wouldnt cause infection in the healthy populations is likely to cause a meningitis infection in a HIV patient?
Cryptococcus neoformans
What group of patients are likely to get listeria infections leading to meningitis?
Immunosuppressed
Neonates
A known alcoholic patient has come in with a headache and fever. You do a lumbar puncture and it shows high neutrophils in the CSF. What is the likely diagnosis?
Pyogenic meningitis with likley streptococcus pneumoniae or listeria
What are the four symptoms that distinguish a patient with meningitis?
Headaches, fever, neck stiffness and change in mental state
Patient has suspected meningitis in the hospital setting. What is your treatment?
Ceftriaxone IV 2g BD
&
Dexamethasone IV 10mg qds over 15-20mins
You suspect a meningitis by listeria what is your treatment?
If not sure its definitely listeria then give
Ceftriaxone IV 2g BD + amoxicillin IV 2g
The amoxicillin is to treat the listeria