Amit Dua DNB, MNAMS, Fellowship in Rheumatology,
Consultant Rheumatologist, MMI Narayana Multi-Speciality Hospital, Raipur and Bilaspur, Chhattisgarh, India.
A. Anti-Ro Ab
B. Severe dental caries
C. Neutropenia
D. Old age
A. Peripheral consolidations on HRCT
B. Basal honeycombing
C. Subpleural reticulation
D. Mosaic attenuation
A. NSIP
B. UIP
C. Lymphocytic interstitial pneumonia (LIP)
D. COP
A. Anti-MDA5-positive patients can develop rapidly progressive ILD even without significant muscle weakness
B. In systemic sclerosis, ILD is more frequent in diffuse cutaneous subsets than in limited cutaneous subsets
C. Pleural effusions are common in SSc-ILD
D. Combination of nintedanib and immunosuppressants is safe and effective in systemic sclerosis ILD
A. SP-D (Surfactant protein)
B. KL-6 (krebs von den Lungen 6)
C. CA 125
D. IL 6
A. Idiopathic inflammatory myopathies
B. Sjogren’s Syndrome
C. Lupus
D. All the above
A. Start immunosuppressive therapy immediately
B. Start antifibrotic therapy immediately
C. Close monitoring with PFTs every 3-6 months
D. Perform bronchoscopy
A. Nintedanib
B. Tocilizumab
C. Cyclophosphamide
D. None
A. Start cyclophosphamide
B. Start mycophenolate mofetil
C. Start nintedanib
D. Start high-dose steroids immediately
A) High-dose corticosteroids and antifibrotics
B) High dose steroids + mycophenolate + antifibrotics
C) Combination of high-dose steroids + mycophenolate ± calcineurin inhibitor
D) Stem cell transplantation
01. C
02. A
03. C
04. C
05. D
06. A
07. C
08. C
09. B
10. C