MLA Paper 1 Flashcards

1
Q

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.

A

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

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2
Q

reflex test to investigate corticospinal tract lesions

A

Hoffman’s sign:

HoFFman - Finger Flick (to see reflex of index finger Exaggerated or not- if exaggerated reflex then UMN lesion)

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3
Q

this differentiates between organic and non-organic lower leg weakness

A

Hoover’s sign

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4
Q

Pernicious anaemia predisposes to what type of cancer

A

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

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5
Q

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

A

POTT’S FRACTURE

like plant pot

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6
Q

A 22-year-old drunk man is involved in a fight. He hurts his thumb when he punches his opponent.

A

Bennett’s fracture

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7
Q

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.

A

COLLEs fracture

Dorsal displacement,

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8
Q

treatment of choice for SLE

A

Hydroxychloroquine

DMARD

SLE
- fatigue
- msk pain
- low mood
- lymphadenopathy

Bloods showed
- anaemia
- leukopenia
- thrombocytopenia

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9
Q

Pathology affcting upper and lower lung zones

A

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

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10
Q

Diabetes insipidus is characterised by a

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

  1. Nephrogenic DI
    –> thiazides
    –> low salt/ protein diet
  2. central diabetes insipidus
    –> desmopressin
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11
Q

Impaired fasting glucose and impaired glucose toelrance

A

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

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12
Q

which medications should be stopped in c.difficile infections?

A

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

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13
Q

What changes in patients with nephrotic syndrome predispose to the development of venous thromboembolism?

A

Loss of antithrombin III

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14
Q

classical biochemical findings in primary hyperparathyroidism

A

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

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15
Q

Confusion, gait ataxia, nystagmus + ophthalmoplegia are features of

A

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

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16
Q

revision card

RIPE ONGO
Rifampicin: Orange secretions
Isoniazid: Neuropathy
Pyrazinamide: Gout
Ethambutol: Optic Neuritis

A

RIPE ONGO
Rifampicin: Orange secretions
Isoniazid: Neuropathy
Pyrazinamide: Gout
Ethambutol: Optic Neuritis

17
Q

HIV serology

A

‘A Gal is for life, a Man is temporary’

IgG vs IgM

18
Q

pain on palpation of the tragus, itching, discharge and hearing loss are classical of

A

Otitis externa

19
Q

Thyrotoxicosis with tender goitre =

A

subacute (De Quervain’s) thyroiditis

There is an initial period of hyperthyroid, due to the release of thyroid hormone from damaged cells. Following the hyperthyroid state, a period of hypothyroid then ensues, eventually resolving back to a euthyroid state.

20
Q
A
21
Q
A