MLA Paper 1 Flashcards
This condition is a severe complication of sickle cell anaemia, characterised by the presence of new pulmonary infiltrates on chest x-ray, accompanied by symptoms such as fever, cough, sputum production, dyspnoea or hypoxia.
Acute sickle chest syndrome
* vaso-occlusion w/i pulmonary microvasculature –> infarction in lung parenchyma
Management
1. pain relief
2. resp support e.g. oxygen therapy
3. Anx
4. tranfusion? may improve oxygenation
reflex test to investigate corticospinal tract lesions
Hoffman’s sign:
HoFFman - Finger Flick (to see reflex of index finger Exaggerated or not- if exaggerated reflex then UMN lesion)
this differentiates between organic and non-organic lower leg weakness
Hoover’s sign
Pernicious anaemia predisposes to what type of cancer
gastric carcinoma
Macro - FAT RBC
folate, alcohol, hypothyroid, reticulocytotic, B12, cytotoxics
normo - 3As and 2Hs
acute blood loss, anaemia of chronic disease, aplastic anaemia
haemolytic anaemia, hypothyroidism
micro - TAILS
thalassaemia, anaemia of chronic disease (more likely to be normo), iron, lead poisoning, sideroblastic
A 14-year-old boy jumps off a 10 foot wall and lands on both feet. An x-ray shows a bimalleolar fracture of the right ankle.
Fracture is
POTT’S FRACTURE
like plant pot
A 22-year-old drunk man is involved in a fight. He hurts his thumb when he punches his opponent.
Bennett’s fracture
A 73-year-old woman presents with pain in her wrist after falling on to an outstretched hand. On examination there is dorsal displacement and angulation. An x-ray shows a transverse fracture of the radius around 2 cm proximal to the radio-carpal joint.
COLLEs fracture
Dorsal displacement,
treatment of choice for SLE
Hydroxychloroquine
DMARD
SLE
- fatigue
- msk pain
- low mood
- lymphadenopathy
Bloods showed
- anaemia
- leukopenia
- thrombocytopenia
Pathology affcting upper and lower lung zones
Upper (CHARTS):
C- Coal worker’s pneumoconiosis
H - Histiocytosis/ hypersensitivity pneumonitis
A - Ankylosing spondylitis
R - Radiation
T - Tuberculosis
S - Silicosis/sarcoidosis
Lower Zone PF (DAIM - chocolate):
D - Drugs
A - Asbestosis
I - Idiopaathic
M - Most connective tissue disorders but AS
Diabetes insipidus is characterised by a
high plasma osmolality and a low urine osmolality
Causes of nephrogenic DI
1. genetic: affcting ADH receptor
2. electrolytes: hypercalcaemia, hypokalaemia
3. lithium: desentizies kidney’s abilities to respond to ADH in collecting ducts
4. Demeclocycline
5. Tubulo-interstitial disease: obstruction, sickle-cell, pyelonephritis
Features
- polyuria
- polydipsia
Investigation
1. high plasma osmolality, low urine osmolality
2. urine osmolality > 700 excludes DI
3. water deprivation test
Management
- Nephrogenic DI
–> thiazides
–> low salt/ protein diet - central diabetes insipidus
–> desmopressin
Impaired fasting glucose and impaired glucose toelrance
A fasting glucose greater than or equal to 6.1 but less than 7.0 mmol/l implies impaired fasting glucose (IFG)
Impaired glucose tolerance (IGT) is defined as fasting plasma glucose less than 7.0 mmol/l and OGTT 2-hour value greater than or equal to 7.8 mmol/l but less than 11.1 mmol/l
which medications should be stopped in c.difficile infections?
opioids
First episode of C. difficile infection
* first-line therapy is oral vancomycin for 10 days
* second-line therapy: oral fidaxomicin
* third-line therapy: oral vancomycin +/- IV metronidazole
Recurrent episode
* recurrent infection occurs in around 20% of patients, increasing to 50% after their second episode
* within 12 weeks of symptom resolution: oral fidaxomicin
* after 12 weeks of symptom resolution: oral vancomycin OR fidaxomicin**
Life-threatening C. difficile infection
* oral vancomycin AND IV metronidazole
* specialist advice - surgery may be considered
What changes in patients with nephrotic syndrome predispose to the development of venous thromboembolism?
Loss of antithrombin III
classical biochemical findings in primary hyperparathyroidism
High serum calcium
low phosphate
PTH may be high or inappropriately normal
Causes of primary hyperparathyroidism
85%: solitary adenoma
10%: hyperplasia
4%: multiple adenoma
1%: carcinoma
Confusion, gait ataxia, nystagmus + ophthalmoplegia are features of
Wernicke’s encephalopathy
Korsakoff’s syndrome
- anterograde / retrograde amnesia, confabulation and apathy
COAT (Wernicke’s encephalopathy), RACK (Korsakoff’s syndrome)
Confusion
Ophthalmoplegia (nystagmus)
Ataxia
Thiamine deficiency
Retrograde amnesia
Anterograde amnesia
Confabulation
Korsakoff’s syndrome