Rheumatology RACP MCQs Flashcards
What is the greatest predictor of future thrombosis in patients with anti-phospholipid syndrome?
A. Annexin Ab
B. Anticardiolipin Ab
C. Lupus anticoagulant
D. Beta 2 glycoprotein 1 Ab
E. Anti-prothrombin Ab
C Lupus anticoagulant
The presence of LA or triple aPL positivity are the main risk factors for recurrence.
A 27 year old lady with SLE presents with recurrent miscarriage. Which antibody predicts further miscarriages?
A. Anti-SSa
B. Anti-histone
C. Anti-cardiolipin
D. Anti-dsDNA
E. Anti-Smith
C - Anticardiolipin
History suggestive of obstetric APS -defined by recurrent miscarriages, late (>10 wks) foetal demise and premature births due to eclampsia/pre-eclampsia and placental insufficiency. Lupus anticoagulant, anti cardiolipin ab and beta2glycoprotein1 ab are characteristic of APS.
In a 75-year-old woman presenting with a unilateral temporal headache, which of the following clinical features is most specific for a diagnosis of temporal arteritis?
A. Temporal artery tenderness.
B. Blurred vision.
C. Jaw (masseter) claudication.
D. Pain and stiffness around the shoulders and hips.
E. Fever.
C. Jaw (masseter) claudication.
50% of patients with GCA have jaw claudication and is the feature most highly associated with a positive biopsy for GCA.
Which of these features has the highest likelihood ratio for giant cell arteritis (GCA)?
A. Headache
B. Diplopia
C. Jaw claudication
D. Joint synovitis
E. Proximal myalgia
C. Jaw claudication
Which of the following cells is most important in the pathogenesis of vasculitis in temporal arteritis?
A. Multinucleate giant cell
B. Macrophage
C. CD8+ T cell
D. CD4+ T cell
E. Dendritic cell
C. CD4+ T cell
Is the cell that initiates differentiation and activation of macrophages and the subsequent granulomatous inflammation.
A 72-year-old man presents with a right sided headache for two weeks. On examination he is tender over the temporal artery. His erythrocyte sedimentation rate (ESR) is 82 mm/hr [0-22].
Which is the most appropriate next investigation?
A. Ultrasound of temporal artery.
B. Temporal artery biopsy.
C. Platelet count.
D. Retinal photography.
E. Serum protein electrophoresis.
B. Temporal artery biopsy.
CDUS of the head, neck, and upper extremities can serve as a diagnostic surrogate for temporal artery biopsy when performed by clinicians skilled in this technique. In the absence of extensive experience with this technology in routine clinical practice, however, temporal artery biopsy remains an essential diagnostic measure for the evaluation of suspected GCA.
A 70-year-old woman, weighing 45 kg, presents with polymyalgia rheumatica and headache. There is a history of osteoporosis with a previous vertebral wedge fracture. Past history also includes hysterectomy.
Temporal artery biopsy reveals giant cell arteritis. A bone mineral density test shows T scores for the lumbar spine and the femoral neck as -3.0 and -2.5 respectively. A chest X-ray shows wedging of the thoracic vertebra on the lateral view.
The most appropriate initial management is:
A. prednis(ol)one 40 mg daily and alendronate 10 mg daily.
B. prednis(ol)one 10 mg daily and azathioprine 100 mg daily.
C. prednis(ol)one 40 mg twice daily and calcitriol 0.25 μg twice daily.
D. prednis(ol)one 15 mg daily and methotrexate 10 mg weekly.
E. prednis(ol)one 40 mg daily and hormone replacement therapy
A. prednis(ol)one 40 mg daily and alendronate 10 mg daily.
GCA treatment - high dose glucocorticoids (40-60 mg) daily
First line treatment of osteoporosis, esp. that caused by steroids - alendronate
A 35 yo woman presents with a 3-day history of headaches and vomiting. She was diagnosed gastrooesophageal reflux disease 12 months ago and Raynaud’s henomenon 2 years ago. On examination her blood pressure is elevated at 225/145 mmHg, her pulse is 80/min. She has changes of sclerodactyly affecting her fingers, dorsum of hands and has evidence of thickened, tight skin over the anterior chest wall.
Relevant investigations are shown below
Hb 110 g/L
WCC 8.5 x 109/L
Platelets 75 x 109/L
Blood film Schistocytes, low platelets
Urea 10 mmol/L
Creatinine 140 umol/L (eGFR 42 ml/min)
U/A: Protein ++, blood and other markers all –ve
Which of the following is the most appropriate treatment?
A. Captopril
B. Sodium nitroprusside
C. Pulse methylprednisolone
D. Cyclophosphamide
A. Captopril
Patient has scleroderma renal crisis - hypertensive crisis, thrombocytopenia, MAHA (micorangiopathic haemolytic anaemia) and proteinuria.
Treatment:
- Rapid correction with Captopril (this is the ACEi of choice because of extensive clinical experience and its short onset and duration of action, which permit rapid dose escalation)
- Intravenous Nitroprusside in ADDTION if there is CNS symptoms
- Dialysis ( 2/3 patients require this)
- Eculizumab (complement pathway antagonist)
- Renal transplant (if unable to wean dialysis >2 yrs)
In systemic sclerosis, which of the following autoantibodies is associated with scleroderma renal crisis?
A. Anti-centromere
B. Anti-topoisomerase
C. Anti-RNA polymerase III
D. Anti-Smith
C. Anti-RNA polymerase III - assc. with diffuse SSc and scleroderma renal crisis
- Anti-centroemere - specific for localised SSc and pulmonary artery hypertension
- Anti-topoisomerase (Anti Scl 70) - specific for diffuse SSc but associated with ILD
Anti-Smith - associated with SLE and MCTD
A 64yo lady presents with sicca symptoms. She has also noted difficult with dorsiflexion of
her right foot, and a tingling sensation in her fingers.
Investigations show :
ANA : 1: 2560
ENAs : positive for SSA(Anti-Ro) and SSB (Anti-La) , negative for dsDNA
RF 85
What is the diagnosis?
A. Rheumatoid arthritis
B. SLE
C. Primary Sjogrens syndrome
D. Overlap syndrome
E. Scleroderma
C. Primary Sjogrens syndrome
ANA - positive in SLE, RA and Sjogrens
Anti Ro/SSA and Anti La/SSB positive in SLE and Sjogrens
dsDNA - specific for SLE
RF positive in RA, SLE and Sjogrens
RACP 2022a Q4
65F with background of Sjogren’s disease. New rash on the lower limbs
(photo given, purpuric, macular, irregular shaped patches mostly <1cm x 1cm in each section, did not look urticarial; looked vasculitic). Associated with loss of sensation over the foot. Investigations list: ANA/SSA/SSB Positive; RF
300; ACPA Neg; p ANCA weak positive. MPO/PR3 neg. HIV/HepB/C negative. Complement (3/4) both low.
a. Hypocomplimentaemic urticarial vasculitis
b. rheumatoid vasculitis
c. mixed cryoglobulinemia
d. microscopic polyangiitis
Answer D Microscopic polyangitis
RACP 2022a Q9
45 year old man developed myopathy on atorvastatin 6 months ago. His CK was normal at the time and his symptoms improved after cessation of the statin. He now presents with worsening proximal myopathy with a CK of
4000. Muscle biopsy demonstrates necrosis, macrophage infiltration and MH1 staining. What is the most likely cause?
a. Immune mediated necrotic myositis
b. Statin toxic myopathy
c. Inclusion body myositis
d. Polymyositis
Answer A IMNM
Initial reaction to statin was likely toxic myopathy
Following this - current reaction with elevated CK, necrosis, macrophage infiltrate and MHC I staining in keeping with immune mediated necrotising myopathy - caused by abs against HMGCR
RACP 2022a Q13
13.A 56 year old woman has autoimmune hepatitis, hypertension and hyperlipidemia on azathioprine, perindopril and atorvastatin. She develops acute joint pain in her left MTP. Joint aspirate showed calcium pyrophosphate (?) crystals. What is your initial management?
a. Allopurinol
b. Probenicid
c. Feboxustat
d. Benzbromarone
Answer B Probenecid
Allopurinol and febuxostat interfere with the metabolism of azathioprine, increasing plasma levels of 6-mercaptopurine which may result in potentially fatal blood dyscrasias.
Benzbromarone reduces hyperuricaemia by blocking renal tubular reabsorption of uric acid. It is also hepatotoxic.
RACP 2022a Q34
34.What is skin lesion associated with antiphospholipid syndrome?
a. Livedo reticularis
b. Digital ulcers
c. Erythema annulare
d. Palpable purpura
Answer A
Livedo is the most common cutaneous manifestation of APS. Although livedo reticularis is nonspecific, livedo racemosa can be associated with arterial lesions and multiple thromboses in APS.
RACP 2022a Q64
64.Testing for which antiphospholipid antibody is affected by warfarin administration?
a. Lupus anticoagulant
b. Anti-cardiolipin
c. Anti-beta2glycoprotein
d. Protein C
Answer A Lupus anticoagulant
aCL and anti-beta2GPI antibody results are unaffected by anticoagulation. By contrast, different anticoagulants have variable effects on laboratory tests used to identify LA, making interpretation of the results more challenging.
RACP 2022b Q25
- A patient on infliximab develops new skin lesions (repeat question - picture shown)
A. Subacute cutaneous lupus
B. Psoriasis
Answer
?A: infiximab can cause drug induced lupus
?B: The use of infliximab in rheumatoid and inflammatory bowel diseases (IBD) has been associated with a variety of adverse skin reactions, including paradoxical psoriatic lesions.
Not enough information recalled to answer question.
RACP 2022b Q 30
- Neonatal heart block is associated with antibodies anti-Ro/SSA and anti-La/SSB.
What period of gestation does neonatal heart block develop?
A. 12-18 weeks
B. 18-24 weeks
C. 24-30 weeks
D. 30-36 weeks
Answer B 18-24 weeks
Congenital heart block is usually detected when the fetus is between 18 and 24 weeks old.
RACP 2022b Q59
- Neonatal heart block is associated with antibodies anti-Ro/SSA and anti-La/SSB.
What period of gestation does neonatal heart block develop?
A. 12-18 weeks
B. 18-24 weeks
C. 24-30 weeks
D. 30-36 weeks
Answer B 18-24 weeks
Congenital heart block is usually detected when the fetus is between 18 and 24 weeks old.
RACP 2021a Q11
Q11. Which of the following features is most specific clinical sign for psoriatic arthritis?
A. Asymmetrical swelling of DIP joints
B. Dactilitis
C. Nail pitting
D. Enthesisits
Answer C
Distal arthritis and arthritis mutilans are considered most specific for PsA, but they are not the most common patterns seen.
RACP 2020a Q41
- 32 yo female with 12 month history of fatigue, arthralgia, sterile dysuria, dry eyes/mouth and
parotid enlargement. CRP: 8, ESR: 90. Had vasculitis screen which showed ANA of 1:640, ENA positive for Anti-Ro/SSa + Anti-La SSb. Rheumatoid factor: 540 and Anti-CCP: 12 (<10).
Lymphopenia and raised globulins. What is the most likely diagnosis?
A) MCTD
B) RA
C) Sjogrens
D) SLE
Answer C Sjogrens
Anti-SSA/Ro and anti-La/SSB are the hallmark antibodies in primary Sjögren’s syndrome (pSS), being present in 60-70% of patients.
RACP 2020a Q77
- Methotrexate used in RA and other inflammatory diseases. Which enzyme does methotrexate
inhibit ?
A) Dihydrofolate reductase
B) Dihyroorotate reductase
C) Inosine monophosphate dehydrogenase
D) Thiopurine methyltransferase
Answer A Dihydrofolate reductase
The inhibition of DHFR by folate antagonists (methotrexate) results in a deficiency in the cellular pools of thymidylate and purines and thus in a decrease in nucleic acid synthesis. Therefore, methotrexate interferes with DNA synthesis, repair, and cellular replication.
RACP 2020
- Recurrent pancreatitis. Enlarged lacrimal glands. Retroperitoneal lymph node enlargement with
dilated bile ducts on imaging. A biopsy of lacrimal glands that shows storiform fibrosis.
A) Sarcoidosis
B) IgG4 disease
C) Lymphoma
D) Sjogren’s Syndrome
Answer B IgG4 disease
The fibrosis associated with IgG4-RD usually has a characteristic “storiform” pattern, typified by a cartwheeling appearance of the arranged fibroblasts and inflammatory cells. The majority of patients have elevated serum levels of IgG4.
RACP 2019a Q4
Question 4
A 35 year old Turkish lady has joint pain, oral and genital ulcers, red painful nodules on legs,
occasional painful red eye. What is the most likely diagnosis?
A. Behcet disease
B. Sarcoidosis
C. Systemic lupus erythematosus
D. Granulomatosis with polyangiitis
Answer A Behcets disease
Behcet disease is an auto-inflammatory systemic vasculitis of unknown etiology. It is characterized by mucocutaneous manifestations, including recurrent oral and genital ulcerations, ocular manifestations, especially chronic relapsing uveitis, and systemic vasculitis involving arteries and veins of all sizes. Tt is observed commonly among populations living along the historic Silk Road, an ancient trading route that spans from Japan and China in the Far East to the Mediterranean Sea, including countries such as Turkey and Iran.
RACP 2019 a Q10
Question 10
Which of the following disease causes predominance of upper lobe pulmonary fibrosis?
A. Rheumatoid arthritis
B. Diffuse scleroderma
C. Mixed connective tissue disease
D. Ankylosing spondylitis
Answer: D Ankylosing spondylitis