Rheumatology Home Internal Medicine 0% 14 votes, 0 avg 56 Rheumatology Welcome to Rheumatology Quiz. There are 50 shot-stemmed, single-best type Rheumatology questions. To get a complete quiz link for free, contact us. 1 / 50 1. Which of the following is the specific antibody for SLE? A. Anti-RNP B. Anti-ssDNA C. Anti-Sm D. Anti-Ro/La 2 / 50 2. Mask-like face is seen in all except: A. Myotonic dystrophy B. Depression C. Parkinsonism D. Scleroderma 3 / 50 3. Penicillamine and colchicine both are used in the treatment of: A. Wilson's disease B. Rheumatoid arthritis C. Progressive systemic sclerosis D. Systemic lupus erythematosus 4 / 50 4. Polyarthritis is the affection of more than: A. 4 joints B. 1 joint C. 2 joints D. 3 joints 5 / 50 5. Reiter’s syndrome is not featured by: A. Circinate balanitis B. Keratoderma blenorrhagica C. Subungual hyperkeratosis D. Pyoderma gangrenosum 6 / 50 6. CREST syndrome is diagnosed by the presence of: A. Anti-centromere antibody B. Anti-histone antibody C. Anti-RNP antibody D. Anti-Jo1 antibody 7 / 50 7. Inhibition of 5-lipoxygenase is beneficial in the treatment of: A. Rheumatoid arthritis B. Bronchial asthma C. Vasculitis D. Hepatorenal syndrome 8 / 50 8. Dystrophic calcinosis is classically seen in: A. Vitamin D toxicity B. Extravasation of calcium salt during injection C. Hyperparathyroidism D. Scleroderma 9 / 50 9. All are extra-articular manifestations of rheumatoid arthritis except: A. Fibrosing alveolitis B. Pericarditis C. ulcerative colitis D. Mononeuritis multiplex 10 / 50 10. Pseudogout may result from all except: A. Hyperphosphatasia B. Gout C. Hemochromatosis D. Ochronosis 11 / 50 11. Terminal interphalangeal joint is classically involved in: A. Reactive arthritis B. Rheumatoid arthritis C. Behcet's syndrome D. Psoriatic arthropathy 12 / 50 12. Oesophagus is most commonly involved by: A. Polymyositis B. Progressive systemic sclerosis C. Behcet's syndrome D. Polyarteritis nodosa 13 / 50 13. Fibromyalgia is characterised by all except: A. High CPK B. Improvement by tricyclic antidepressant C. Female preponderance D. Focal point tenderness 14 / 50 14. HBsAg may be present in which vasculitis? A. Henoch-Schonlein purpura B. Churg-Strauss syndrome C. Temporal arteritis D. Polyarteritis nodosa 15 / 50 15. Which organ involvement is not included within the classic triad of Wegener’s granulomatosis? A. Lower respiratory tract B. Kidney C. Cardiovascular system D. Upper respiratory tract 16 / 50 16. Clutton’s joint is characteristic of: A. Tabes dorsalis B. Chondrocalcinosis C. Congenital syphilis D. Diabetes mellitus 17 / 50 17. Progressive systemic sclerosis (PSS) may develop in all except: A. Alveolar cell neoplasm B. Heart block C. Pulmonary hypertension D. Hypertrophic cardiomyopathy 18 / 50 18. ANA is positive in SLE in approximately: A. 70% cases B. 60% cases C. 95% cases D. 80% cases 19 / 50 19. ‘Pathergy’ is characteristic of: A. Reiter's syndrome B. Lyme arthritis C. Leucocytoclastic vasculitis D. Behcet's syndrome 20 / 50 20. Which of the following is usually not a skin lesion of SLE? A. Erythema nodosum B. Panniculitis C. Bullous lesion D. Periungual erythema 21 / 50 21. Eosinophilic fasciitis is associated with all except: A. Excessive consumption of L-tryptophan B. Eosinophilia C. Usually a self-limiting disease D. Raynaud's phenomenon 22 / 50 22. HLA B-27 is usually detected in all except: A. Ankylosing spondylitis B. Reactive arthritis C. Systemic lupus erythematosus D. Psoriatic arthritis 23 / 50 23. Jaccoud’s arthropathy is not characteristic of: A. Rheumatic fever B. Sarcoidosis C. Reiter's syndrome D. Systemic lupus erythematosus 24 / 50 24. Heberden’s node is seen in: A. Osteoarthritis B. Progressive systemic sclerosis C. Dermatomyositis D. Gout 25 / 50 25. Hyperostosis is seen in all except: A. Hyperthyroidism B. Primary hyperparathyroidism C. Acromegaly D. Paget's disease 26 / 50 26. Finkelstein’s test is positive in: A. De Quervains' tenosynovitis B. Cervical rib C. Dupuytren's contracture D. Ankylosing spondylitis 27 / 50 27. Bouchard’s nodes in osteoarthritis are seen in: A. Metacarpophalangeal joint B. Proximal interphalangeal joint C. Carpometacarpal joint D. Distal interphalangeal joint 28 / 50 28. Raynaud’s phenomenon may be treated by: A. Naftidrofuryl B. Dimethyl sulfoxide C. Methysergide D. Propranolol 29 / 50 29. Temporal arteritis is featured by all except: A. Jaw claudication B. Bell's palsy C. May develop permanent blindness D. Intense headache 30 / 50 30. Example of autoimmune arthritis is: A. Psoriatic arthritis B. Haemophilic arthritis C. Rheumatoid arthritis D. Osteoarthritis 31 / 50 31. Churg-Strauss syndrome commonly manifests as: A. Epistaxis B. Allergic rhinitis C. Sinusitis D. Raynaud's phenomenon 32 / 50 32. Rose-Waaler test (RF) is positive in rheumatoid arthritis in: A. 45% cases B. 30% cases C. 90% cases D. 70% cases 33 / 50 33. Which organ involvement does not occur in progressive systemic sclerosis? A. Central nervous system B. Pulmonary C. Cardiac D. Renal 34 / 50 34. Angioneurotic oedema may be treated by: A. Diuretics B. Danazol C. Tropical corticosteroid D. Mineralocorticoids 35 / 50 35. In rheumatoid arthritis, rheumatoid factor is formed against: A. lgM B. IgD C. lgG D. IgA 36 / 50 36. c-ANCA (antinuclear cytoplasmic antibody) is diagnostic of: A. Wegener's granulomatosis B. Crescentic glomerulonephritis C. Polyarteritis nodosa D. Microscopic polyarteritis 37 / 50 37. Hypertrophic osteoarthropathy is most commonly due to: A. Fibrosing alveolitis B. Bronchogenic carcinoma C. Mesothelioma of pleura D. COPD 38 / 50 38. Hypertrophic osteoarthropathy is least common in: A. Pachy dermoperiostitis B. Metastatic tumour of lung C. Bronchogenic carcinoma D. Mesothelioma of pleura 39 / 50 39. Which of the following is not an extra-articular manifestation of ankylosing spondylitis? A. Raynaud's phenomenon B. Amyloidosis C. Acute pulmonary fibrosis D. Aortic incompetence 40 / 50 40. Which of the following usually presents as monoarthropathy? A. Rheumatoid arthritis B. Sjogren's syndrome C. Gout D. SLE 41 / 50 41. Which of the following is commonly involved in Paget’s disease? A. Pelvis B. Skull C. Phalanges D. Long bones of extremities 42 / 50 42. Hereditary angioneurotic oedema is due to: A. Deficiency of leukotrienes B. C1 esterase inhibitor deficiency C. Excess of prostaglandin D2 D. Hypocomplementemia C2 43 / 50 43. Still’s disease is classically associated with all except: A. Involvement of metacarpophalangeal joints B. Negative Rose-Waaler test C. Maculopapular rash D. Sacroiliitis 44 / 50 44. Felty’s syndrome is not associated with: A. Lymphadenopathy B. Vasculitis C. Thrombocytopenia D. Age of onset 20-25 yrs 45 / 50 45. HLA-B27 tissue typing is not associated with: A. Behcet's syndrome B. Ankylosing spondylitis C. Psoriatic arthropathy D. Reiter's syndrome 46 / 50 46. Seronegative arthropathy is not associated with: A. Sacroiliitis B. Mononeuritis multiplex C. Iritis D. Enthesopathy 47 / 50 47. Sickle cell anaemia may be complicated by all except: A. Osteomyelitis B. Avascular necrosis of bone C. Dactylitis D. Polyarthritis 48 / 50 48. Osteosclerosis of the spine may be seen in all except: A. Hodgkin's disease B. Osteopetrosis C. Osteomalacia D. Fluorosis 49 / 50 49. Which of the following is recognised extra-articular manifestation of ankylosing spondylitis? A. Acute pulmonary fibrosis B. Mitral stenosis C. Mononeuritis multiplex D. Pericarditis 50 / 50 50. Still’s disease does not give rise to: A. Maculopapular rash B. Lymphadenopathy C. Splenomegaly D. Positive Rose-Waaler test LinkedIn Facebook Twitter VKontakte Visit our FB page Restart Quiz Send Feedback Previous Post Gastroenterology Next Post ECG Quiz