Diagnosis: rash, arthritis and acute glomerulonephritis?
IgA vasculitis (also known as Henoch–Schönlein purpura)
What does sudden-onset neurological symptoms with rapid worsening and drowsiness suggest?
A vascular cause with an expanding space-occupying lesion causing rising intracranial pressure and risk of herniation
Why is cerebellar haemorrhage considered a neurological emergency?
Because its location in the posterior fossa can lead to rapid deterioration due to raised intracranial pressure and potential brainstem compression
What features differentiate cerebellar haemorrhage from subdural haemorrhage?
Sudden onset with vomiting, gait unsteadiness, and rapidly worsening drowsiness are more typical of cerebellar haemorrhage; subdural haemorrhage usually has a slower progression unless acute
What is the most likely diagnosis in a 79-year-old woman with pallor, 2-cm splenomegaly, small axillary lymph nodes, Hb 107 g/L, WCC 34.5 × 10^9/L, and platelets 183 × 10^9/L?
Chronic lymphocytic leukaemia (CLL)
What clinical and lab features make chronic lymphocytic leukaemia more likely than acute myeloid leukaemia, chronic myeloid leukaemia, myelodysplasia, or myelofibrosis?
CLL is suggested by splenomegaly, anaemia, lymphadenopathy, and high white cell count; AML usually presents acutely with thrombocytopenia, CML with very high platelets, myelodysplasia usually has low WCC, myelofibrosis often has abnormal blood counts including low WCC or platelets
Why would a white cell differential be requested in suspected chronic lymphocytic leukaemia?
To help confirm lymphocytosis and the characteristic morphology of lymphocytes, aiding diagnosis and differentiating from other myeloproliferative disorders
What glomerular abnormality is most likely at renal biopsy in a 17-year-old boy with non-blanching rash, swollen knee, visible haematuria, proteinuria, and raised creatinine?
Mesangial deposition of IgA (IgA vasculitis/Henoch–Schönlein purpura)
Which glomerular abnormalities are associated with other diseases and help differentiate them from IgA vasculitis?
Foot process effacement: nephrotic syndrome; Linear IgG deposition: anti-GBM disease; Thickened basement membranes: Alport syndrome; Focal segmental sclerosis: FSGS
In a 37-year-old woman with intermittent lightheadedness, normal examination, and a 24-hour ECG showing atrial and ventricular premature beats, nocturnal bradycardia, Mobitz type I AV block, and supraventricular tachycardia, which finding is clinically most important?
Supraventricular tachycardia
Why can stool cultures be negative in giardiasis despite infection?
Because Giardia cysts are shed intermittently, making standard stool cultures and microscopy sometimes falsely negative
What is the characteristic pattern of hair loss in alopecia areata?
Discrete, non-scaly patches of hair loss without scarring
How can alopecia areata be differentiated from trichotillomania, lupus, hypothyroidism, and seborrhoeic dermatitis?
Trichotillomania: short hairs of same length; Lupus: scarring and inflammation; Hypothyroidism: diffuse thinning with brittle hair; Seborrhoeic dermatitis: diffuse scaling rather than discrete patches
What is a common cardiac cause of recurrent, short-lasting episodes of collapse in a patient with previous myocardial infarction?
Ventricular tachycardia
What ECG findings suggest a left ventricular aneurysm post-myocardial infarction?
Persistent ST-segment elevation with Q waves in the affected territory
What is the characteristic feature of an Adie’s (tonic) pupil?
A dilated pupil that reacts very slowly to light but constricts slowly on accommodation + Reduced or absent deep tendon reflexes
How can Adie’s pupil be differentiated from afferent pupillary defect, Argyll Robertson pupil, Horner’s syndrome, and third cranial nerve palsy?
Afferent defect: paradoxical dilatation with swinging torch test; Argyll Robertson: accommodates but does not react, usually bilateral; Horner’s: small pupil with ptosis; Third nerve palsy: ptosis with pupillary involvement and often eye movement abnormalities
What is the role of urinary citrate in preventing kidney stones?
Citrate binds calcium to form soluble complexes and inhibits crystal growth and aggregation, reducing calcium stone formation
What therapy is most useful to reduce recurrent calcium stone formation in patients with low urinary citrate?
Potassium citrate supplementation
Why are thiazides, allopurinol, penicillamine, and low-calcium diets not first-line in patients with low urinary citrate and normal serum calcium?
Thiazides are indicated for hypercalciuria; allopurinol is for uric acid stones; penicillamine is for cystine stones; low-calcium diets can increase oxalate absorption and worsen stones
What is the most common inherited bleeding disorder that can present with excessive bleeding after dental procedures or minor surgery?
Von Willebrand disease (vWD)
How can von Willebrand disease be differentiated from factor V Leiden, factor IX deficiency, factor XII deficiency, and antiphospholipid syndrome?
Factor V Leiden and antiphospholipid syndrome: increased thrombosis risk, not bleeding; Factor IX deficiency: X-linked, mainly males; Factor XII deficiency: prolonged aPTT without bleeding tendency
Most likely complication of cocaine use causing agitation, chest pain, hypertension?
Hyperthermia
Sympathomimetic effects can elevate body temperature and cause rhabdomyolysis.
What is the normal function of α1-antitrypsin?
It inhibits neutrophil elastase, protecting alveolar tissue from proteolytic damage.