I. Start the exam by click the “Start” button
Interstitial Lung Diseases- Part 3
See all quizzes of Obstructive Pulmonary Disease at here:
1.Most common form of pulmonary involvement in connective tissue disorders is ?
A. Respiratory bronchiolitis
B. Desquamative interstitial pneumonia
C. Cryptogenic organizing pneumonia
D. Nonspecific interstitial pneumonia
Commonest form of pulmonary involvement in connective tissue disorders is nonspecific interstitial
pneumonia.
2. Rheumatoid pneumoconiosis is also called ?
A. Hermansky-Pudlak syndrome
B. Churg-Strauss syndrome
C. Caplan’s syndrome
D. Goodpasture’s syndrome
3. Most common pulmonary manifestation in Systemic Lupus Erythematosus (SLE) is ?
A. Atelectasis
B. Pleuritis
C. Pulmonary vascular disease
D. Infectious pneumonia
4. ILD occurs more commonly in the subgroup of polymyositis & dermatomyositis patients having which antibody ?
A. Anti-Smith antibody
B. Anti-Ro antibody
C. Anti-Jo-1 antibody
D. Anti-La antibody
5. Which of the following about pulmonary alveolar proteinosis (PAP) is false ?
Harrison’s 18th Ed. 2168
A. Impaired ability to process surfactant
B. Accumulation of PAS positive lipoproteinaceous material in
distal air spaces
C. Extensive lung inflammation
D. Preserved lung architectur
6. In pulmonary alveolar proteinosis (PAP), the neutralizing IgG antibody is against which of the following ?
A. Surfactant
B. GM-CSF
C. PAS positive lipoproteinaceous material
D. All of the above
7. Which of the following is the most common class of Pulmonary Alveolar Proteinosis (PAP) ?
A. Acquired
B. Congenital
C. Secondary
D. None of the above
8. Secondary pulmonary alveolar proteinosis (PAP) is caused by which of the following malignancies ?
A. Lung
B. Pleural
C. Hematopoietic
D. Hepatic
9. Secondary PAP is caused by ?
A. Lysinuric protein intolerance
B. Acute silicosis
C. Hematopoietic malignancies
D. All of the above
10. Congenital PAP is caused by mutation in ?
A. SP-A gene
B. SP-B gene
C. SP-C gene
D. SP-D gene
11. In PAP, which of the following is frequent ?
A. Polycythemia
B. Hypergammaglobulinemia
C. Increased LDH
D. All of the above
.
12. Radiographically, ‘bat-wing’ distribution of lung opacities is suggestive of which of the following ?
A. Churg-Strauss syndrome
B. Pulmonary lymphangioleiomyomatosis (LAM)
C. Pulmonary alveolar proteinosis (PAP)
D. Goodpasture’s syndrome
13. Pulmonary lymphangioleiomyomatosis (LAM) is seen in ?
A. Female child
B. Premenopausal women
C. Postmenopausal women
D. Any of the above
14. In Pulmonary lymphangioleiomyomatosis (LAM), there occurs proliferation of which of the following ?
A. Type 1 pneumocytes
B. Type 2 pneumocytes
C. Pulmonary lymphatic vessels
D. Atypical pulmonary interstitial smooth muscle
15. Atypical smooth-muscle cells that proliferate in pulmonary lymphangioleiomyomatosis (LAM) react with which of the following monoclonal antibody ?
A. HMB42
B. HMB43
C. HMB44
D. HMB45
16. Which of the following modalities of treatment is useful in Pulmonary lymphangioleiomyomatosis (LAM) ?
A. Oophorectomy
B. Progesterone
C. Tamoxifen
D. All of the above
17. Which of the following is not a type of diffuse interstitial disease ?
A. Pneumoconiosis
B. Hypersensitivity pneumonitis
C. Eosinophilic granuloma
D. Acute respiratory distress syndrome
18. Which of the following is not a type of diffuse alveolar disease ?
A. Cardiogenic pulmonary edema
B. Acute respiratory distress syndrome
C. Sarcoidosis
D. Eosinophilic granuloma
19. Injury to which of the following leads to hemoptysis in Diffuse Alveolar Hemorrhage ?
A. Arterioles
B. Venules
C. Capillaries
D. Any of the above
20. Which of the following is increased in Diffuse Alveolar Hemorrhage (DAH) ?
A. PaO2
B. PAO2
C. DlCO
D. PaCO2
21. Immune complexes are absent in examination of lung or renal tissue by immunofluorescent techniques in ?
A. Granulomatosis with polyangiitis (Wegener’s)
B. Microscopic polyangiitis pauci-immune
glomerulonephritis
C. Isolated pulmonary capillaritis
D. All of the above
22. Linear deposition of immune complexes is seen in examination of lung or renal tissue by immunofluorescent techniques in ?
A. SLE
B. Goodpasture’s syndrome
C. Henoch-Schönlein purpura
D. Wegener’s granulomatosis
23. Inherited diseases that produce interstitial lung disease include ?
A. Tuberous sclerosis
B. Neurofibromatosis
C. Niemann-Pick disease
D. All of the above
24. Inherited diseases that produce interstitial lung disease include ?
A. Gaucher’s disease
B. Hermansky-Pudlak syndrome
C. Niemann-Pick disease
D. All of the above
25. Which of the following is false about bronchocentric granulomatosis (BG) ?
A. Descriptive clinical term
B. Hypersensitivity reaction to Aspergillus
C. Peripheral blood eosinophilia
D. CxR may show irregularly shaped mass lesions
26. Bronchocentric granulomatosis (BG) is associated with which of the following pulmonary condition ?
A. Asthma
B. Bacterial pneumonia
C. Pleural effusion
D. Primary spontaneous pneumothorax
27. Treatment of choice in bronchocentric granulomatosis is ?
A. Glucocorticoids
B. Chemotherapy
C. Surgery
D. Radiation
28. Which of the following is not a cause of solitary circumscribed pulmonary nodule ?
A. Wegener’s granulomatosis
B. Bronchogenic cyst
C. Vascular malformation
D. Sarcoidosis
29. Which of the following is not a cause of diffuse nodular pulmonary disease ?
A. Metastatic neoplasm
B. Sarcoidosis
C. Pneumoconiosis
D. Eosinophilic granuloma
30. Pulmonary hemorrhage syndromes include ?
A. Goodpasture’s syndrome
B. Idiopathic pulmonary hemosiderosis
C. Isolated pulmonary capillaritis
D. All of the above
31. Gastrointestinal / liver diseases that can produce interstitial lung disease include ?
A. Crohn’s disease / ulcerative colitis
B. Primary biliary cirrhosis
C. Chronic active hepatitis
D. All of the above
