Mixed Topics Flashcards
(219 cards)
What does release of CCK lead to?
- GB squeezes
2. sphincter of Oddi relaxes
Describe the pain in biliary colic
RUQ (and epigastric) pain that may radiate to the shoulder; “dull” pain
increases in severity over 15 minutes and then reaches a plateau (normally for less than 6 hours) until the gallstone dislodges and the pain subsides.
the pain starts several hours after a meal but may also be worse at night because it is easier for the gallstone to become lodged when lying flat.
What are the histological features of UC, CD and Coealic disease?
UC: continuous distal disease, mucin depletion, basal plasmacytosis, diffuse mucosal atrophy, absence of granulomata, and anal sparing. crypt branching/spaarcity.
CD: transmural involvement with non-caseating granulomas. Significant inflammation in the colonic wall, widening of submucosa, and dense lymphoid aggregates in the submucosa. Cryptitis with morphological distortion of the crypts accompanied by inflammation and abundant lymphatic and plasma cells. lymphoid aggregates.
(intestinal biopsy is confirmative rather than diagnostic).
Coeliac: villous atrophy
What are the layers of the skull/
- Skin
- aponeurosis
- Periosteum
- Bone / cranium
- Dura Mater (periosteal and meningeal layer)
- Arachnoid Mater
- Pia mater
- Brain (grey matter and white matter)
What is Rigler’s triad?
Rigler triad of gallstone ileus, pneumobilia (air in the
biliary tract, low small bowel obstruction with distended
small bowel loops, and an impacted gallstone in the terminal ileum.
It is an unusual complication of cholecystolithiasis and chronic cholecystitis.
What are the ECG features of WPW syndrome?
- short PR interval (<120ms)
- wider QRS (>110ms)
- delta waves (lead V1 +ve in type A, -ve in type B)
- you may also get ST-segment and T wave deflection in the direction opposite of the QRS.
What are the A to J signs of liver failure?
· Asterixis · Bruising · Clubbing · Dupuytren's contracture · Erythema (palmar) · Fetor hepaticus (breath has a strong, musty smell) · Gynaecomastia · Hepatomegaly (in early cirrhosis) · Itching · Jaundice
Do you get koilonychia in cirrhosis?
No - koilonychia (spooning of the nails) occurs in chronic iron deficiency
It is associated with Plummer-vinson syndrome - a disease characterised by the formation of oesophageal webs leading to dysphagia.
Name the 5 organisms that cause bloody diarrhoea
There are 5 common organisms that cause bloody diarrhoea - the CHESS organisms · Campylobacter jejuni · Haemorrhagic E.coli (O157)** · Entamoeba histolytica · Salmonella · Shigella
**most common cause of travellers diarrhoea; can be found in Thailand.
Name 3 conditions that pre-dispose you to SAH
- PKD (autosomal dominant condition with bilaterally enlarged kidneys, HTN and haematuria)
- Marfan’s syndrome
- Ehler Danlos syndrome
What are the 6 Ps of acute limb ischamia?
- pale
- pulseless
- pallor
- power loss or paralysis
- paraesthesia
- perishingly cold
Name UMN and LMN signs
UMN:
- spasticity/increased muscle tone
- hyperreflexia
- clonus
- Babinski’s sign
- NO muscle atrophy because LMN are still intact and supply the muscles with nutrients, however over time there will be a degree of muscle atrophy due to disuse
LMN:
- hypotonia
- hyporeflexia
- muscle atrophy
- Fasciculations (visible twitches in the muscle caused by damaged motor units firing spontaneous, uncoordinated APs
- Fibrillations (twitches of individual muscle fibres that can be observed using EMG but not by the naked eye)
What are the ECG findings of a patient with a PE?
- sinus tachycardia
- S1Q3T3 ( dep S wave in lead 1, pathological Q wave in lead 3, inverted T wave in lead 3)
- right ventricular strain (RBBB, right axis deviation)
Describe the gait of a patient with PD
- narrow based gait which is stooped and shuffling with reduced arm swing.
Description of a BCC vs SCC
BCC: rolled, pearly edges
SCC:
Summarise the criteria for MS Dx very briefly
Absence of alternative diagnosis
Dissemination in time (DIT)
Dissemination in space (DIS)
– but could definitely say “oligoclonal bands were present in the CSF but not the serum”
Describe when you would see the following gaits:
- ataxic
- hemiplegic
- scissor gait
- choreiform
- shuffling
- Ataxic gait is cerebellar sign, seen in Wernicke’s encephalopathy.
- Hemiplegic is typically following a stroke
- Scissor gait characteristic of cerebral palsy
- Choreiform (dance like) typical of Huntington’s
- shuffling, narrow gait, stooped with reduced arm swing is characteristic of PD
Describe when you would see the following gaits:
- ataxic
- hemiplegic
- scissor gait
- choreiform
- shuffling
- Ataxic gait is cerebellar sign, seen in Wernicke’s encephalopathy.
- Hemiplegic is typically following a stroke
- Scissor gait characteristic of cerebral palsy
- Choreiform (dance like) typical of Huntington’s
- shuffling, narrow gait, stooped with reduced arm swing is characteristic of PD
Name the triad of Sx in PD as well as the 6Ms
Classical parkinsonism triad
Bradykinesia
Rigidity
Rest tremor
6Ms Monotonous, hypotonic speech Micrographia HypomiMesis (expressionless face) March a petit pas Misery → depression Memory loss → dementia
Motor: Tremor, Rigidity, Akinesia &
Bradykinesia, clumsiness, loss of postural reflexes,
falls, dystonia, cramps
Neuropsychiatric: Hallucinations, Anxiety,
Confusion, Stupor, Impulsivity, Depression,
Cognitive decline, Dementia, Paranoia,
Visuospatial dysfunction
Autonomic & Vegetative: Bladder, Bowel,
Hypotension, Impotence, Dysarthria,
Dysphagia, Drooling, Rash, Anosmia
Sleep: Restless Legs, REM Sleep disorder,
PLMD, Nightmares, Nocturia, Immobility, Pain
What is the most common cause of Parkinsonism and what are some other causes?
- PD is the most common cause (due to loss of DA-ergic neurones is the substantia nigra )
- drug induced (e.g. antipsychotics and anti-emetics that lower DA levels)
- atypical Parkinsonism (e.g. multi-infarct Parkinson’s, where the symptoms are a result of one or more strokes in the striatum area, not due to neurodegenerative loss of dopaminergic neurones)
Summarise fronto-temporal dementia:
- also known as Pick’s disease
- Personality change
- Disinhibition
- Overeating, preference for sweet foods
- Emotional blunting
- Relative preservation of memory
- Tauopathy (Pick bodies: Hyperphosphyorlated tau protein)
- 40-60yrs
- Also typically affects people younger than in other dementias
- ±FHx (although most are sporadic)
- Death within 5-10yrs
Summarise the main features of Wernicke’s encephalopathy
ACE
- ataxia (due to cerebellar damage)
- confusion
- eye signs (ophthalmoplegia, nystagmus, diplopia, ptosis)
- alcoholism
- malnourishment
Wernicke-Korsakoff syndrome is collection of acute neurological signs arising from lack of vitamin B1 (thiamine).
Classically there us a triad of symptoms listed above. But only 10% of patients will present with all 3 symptoms
Alcoholism is the no. 1 cause of WKS because people with the condition generally have a poor diet. Alcohol also prevents vitamin B-1 absorption and storage.
Which drugs worsen the Sx of myasthenia gravis?
- beta blockers
- lithium
- several Abx
- several antimalarials
What are the BTS criteria for a severe asthma attack?
PEF <33% expected
<92% SpO2
PaO2 <8 kPa