MRCP OFFICIAL PAPER Flashcards
What glomerular abnormality is seen in IgA vasculitis (HSP)?
Rash (non blanching)
Arthritis
Acute glomerulonephritis
- Mesangial deposition of IgA
In which condition is foot process effacement seen on renal biopsy?
Nephrotic syndrome.
In which condition is linear deposition of IgG on basement membrane seen on renal biopsy?
Anti-glomerular basement membrane disease.
In which condition is thickening of basement membranes seen on renal biopsy?
Alport Syndrome.
Hepatitis B serology in patient with previous immunisation to hep B?
positive anti-hepatitis B surface antibody but all others negative.
Antibody for antiphospholipid syndrome?
Anticardiolipin antibodies.
The livedo reticularis, cognition problems and loin pain are a result of thrombosis.
1-month history of weight loss, abdominal distension, flatulence and foul-smelling diarrhoea following a visit to India?
Giardiasis
Laboratory finding in Wilson’s disease?
- Low serum caeruloplasmin concentration.
- Free (non-ceruloplasmin-bound) serum copper is increased.
- Increased urinary copper excretion
- Reduced total serum copper (counter-intuitive, but 95% of plasma copper is carried by ceruloplasmin).
Levels of caeruloplasmin are low in most cases. Hepatic, serum and urinary copper levels are all elevated. Caeruloplasmin is the molecule by which about 95% of copper is normally carried.
Wilson’s disease is an autosomal recessive disorder characterised by excessive copper deposition.
commonly presents with hepatic, neurological and psychiatric signs and symptoms.
Kayser-Fleischer rings.
Mx Penicillamine.
Lactose is broken down into what by lactase?
Glucose + Galactose
Sucrose is broken down into what by Sucrase?
Glucose + Fructose
Maltose is broken down into what by maltase?
Glucose + Glucose
16-year-old girl presented with non-scaly, discrete areas of hair loss on the scalp. She had a history of atopic eczema and had a number of depigmented areas on her hands and around her eyes.
What is the most likely diagnosis?
Alopecia Areata.
Alopecia areata is an immunologically based disorder where there are discrete areas of hair loss but WITHOUT scarring or scaling, and patients with this condition have a higher incidence of atopic eczema.
Lupus erythematosus - there is usually active inflammation with scarring
Trichotillomania - there are residual short hairs at the affected site, because the patient generally finds it difficult to pull newly growing hairs.
Seborrhoeic dermatitis generally gives diffuse scaling on the scalp without hair loss; although it can cause some areas of hair loss, this would be associated with scaling of the scalp.
Features of Adie’s tonic pupil?
Holmes-Adie pupil is a benign condition most commonly seen in women. It is one of the differentials of a dilated pupil.
- Unilateral
- DILATED pupil
- Once the pupil has constricted it remains small for an abnormally long time
- Slowly reactive to accommodation
- Does NOT react to light (very poorly)
Holmes-Adie syndrome:
association of Adie’s tonic pupil with absent ankle/knee reflexes
Features of afferent pupillary defect?
An afferent pupillary defect is due to impaired ipsilateral optic nerve function, causing brief paradoxical pupillary dilatation to light with the “swinging torch” test
Features of Argyll Robertson pupils?
Argyll Robertson pupils accommodate but do not react and are typically bilaterally SMALL.
a.k.a prostitute pupil:
They both “accommodate, but don’t react“, and both are associated with neurosyphilis.
Features of third nerve palsy?
- Eye is deviated down and out
- Ptosis
- Dilated pupil (mydriasis)
Mx for recurrent renal stone?
Urinary citrate reduces urinary supersaturation of calcium salts by forming soluble complexes with calcium ions, and by inhibiting crystal growth and aggregation, hence the use of potassium citrate in recurrent stone formation.
Calcium stones may be due to hypercalciuria - thiazides diuretics (increase distal tubular calcium resorption).
Prevention for oxalate stones?
Cholestyramine and Pyridoxine reduces urinary oxalate secretion.
Low-calcium diets lead to increased oxalate absorption production, which is counterproductive.
Most common thrombophilia condition?
Factor V Leiden (activated protein C resistance) is the most common inherited thrombophilia.
Most common bleeding disorder?
Von Willebrand’s disease is the most common inherited bleeding disorder. The majority of cases are inherited in an autosomal dominant fashion and characteristically behaves like a platelet disorder i.e. epistaxis, bleeding after dental extraction and menorrhagia are common whilst haemoarthroses and muscle haematomas are rare.
Prolonged bleeding time
APTT may be prolonged
Alpha-1 antitrypsin deficiency phenotype?
Patients who manifest disease usually have ZZ genotype.
The S genotype is an intermediate deficiency and M is normal, Z is severe.
normal: MM
heterozygous: MZ
homozygous SS: 50% normal A1AT levels
homozygous ZZ: 10% normal A1AT levels
Most common thyroid cancer?
Papillary carcinoma.
Often young females - excellent prognosis.
Mx:
- Total thyroidectomy
followed by radioiodine (I-131) to kill residual cells
Feature of follicular adenoma?
Usually present as a solitary thyroid nodule.
Features of medullary carcinoma?
Cancer of parafollicular (C) cells
- Serum Calcitonin levels are raised. (Calcitonin lowers blood calcium levels by suppressing osteoclast activity)
- Part of MEN-2
Features of anaplastic thyroid carcinoma?
- Most common in elderly females
- Local invasion is a common feature.
- Causes pressure symptoms.
Bone pain with normal calcium, phosphate and raised ALP?
Paget’s disease.
Blood results in osteomalacia?
- Low vitamin D levels
- Low calcium
- Low phosphate
- Raised ALP
How does allopurinol precipitate acute gout?
Urate-lowering therapy commonly leads to acute flares of gout, thought due to falling serum urate levels leading to uric acid crystals detaching from articular cartilage. It’s good practice to offer prophylaxis with NSAID or colchicine for the first 6 months of allopurinol therapy.
Gene abnormality in Burkitt’s lymphoma?
Burkitt’s lymphoma is associated with the C-Myc gene overexpression. Chromosome 8 and 14.
JAK2 mutation associated with which condition?
JAK2 mutations are associated typically with myeloproliferative disease in particular primary polycythaemia.
Which condition associated with BCR-ABL gene?
BCR-ABL is associated with chronic myeloid leukaemia.