Case 1: Question. 1.1 What is the main pattern of this HRCT? 1. Intralobular line 2. Groundglass opacity 3. Perilymphatic nodule

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Transcription:

HRCT WORK SHOP

Case 1

Case 1: Question 1.1 What is the main pattern of this HRCT? 1. Intralobular line 2. Groundglass opacity 3. Perilymphatic nodule

Case 1: Question 1.2 What is the diagnosis? 1. Hypersensitivity pneumonitis 2. Silicosis 3. Alveolar proteinosis 4. Miliary tuberculosis

Case 2

Case 2 : Question 2.1 What is the main pattern of this HRCT? 1. Nodule 2. Groundglass opacity 3. Reticular line

Case 2 : Question 2.2 What is the intralobular distribution? 1. Centrilobular 2. Perilymphatic 3. Random

Case 2 : Question 2.3 What is the diagnosis? 1. Hypersensitivity pneumonitis 2. Silicosis 3. Lymphangitic carcinomatosis 4. Miliary tuberculosis

Case 3

Case 3 : Question 3.1 What about the lung volume? 1. Increase 2. Normal 3. Decrease

Case 3 : Question 3.2 What is the intralobular distribution? 1. Centrilobular 2. Perilymphatic 3. Random

Case 4

Case 4: Question 4.1 What is the intralobular distribution? 1. Centrilobular 2. Perilymphatic 3. Random

Case 4: Question 4.2 What is the associated finding? 1. Bronchiectasis 2. Lymphadenopathy 3. Pleural effusion

Case 4: Question 4.3 What is the diagnosis? 1. Bronchial spreading tuberculosis 2. Miliary tuberculosis 3. Lymphangitic carcinomatosis

Case 5

Case 5: Question 5.1 What is the main pattern of this HRCT? 1. Micronodule 2. Line 3. Both 1 and 2

Case 5: Question 5.2 What is the intralobular distribution? 1. Centrilobular 2. Perilymphatic 3. Random

Case 6

Case 6: Question 6.1 What is this CT sign? 1. Crazy paving 2. Mosaic pattern

Case 7

Case 7: Question 7.1 What is the craniocaudal distribution? 1. Upper + middle 2. Lower + middle 3. Diffuse

Case 7: Question 7.2 What is the diagnosis? 1. Emphysema 2. Langerhans cell histocytosis (LCH) 3. Lymphangiomyomatosis (LAM)

Case 8

Case 8: Question 8.1 What is the main pattern of this HRCT? 1. Honeycomb 2. Groundglass opacity 3. Consolidation

Case 9

Case 9: Question 9.1 What is the diagnosis? 1. Emphysema 2. Langerhans cell histocytosis(lch) 3. Lymphangiomyomatosis (LAM)

Case 10

Case 10: Question 10.1 What is the main pattern of this HRCT? 1. Smooth septal thickening 2. Nodular septal thickening 3. Centrilobular nodule

Case 10: Question 10.2 What is the associated finding? 1. Pleural effusion 2. Pulmonary arterial hypertension 3. Lymphadenopathy

Case 11

Case 11: Question 11.1 What is the main pattern of this HRCT? 1. Smooth interlobular septal thickening 2. Nodule 3. Ground glass opacity

Case 11: Question 11.2 What is the pattern of disease spreading? 1. Perilymphatic spreading 2. Bronchial spreading

Case 11: Question 11.3 What is the associated finding? 1. Pleural effusion 2. Enlarged lymph node 3. 1 and 2

Case 11: Question 11.4 What is the diagnosis? 1. PAP 2. Hypersensitivity pneumonitis 3. Lymphangitic carcinomatosis

Case11 : Question 11.5 What is the best further investigation? 1. Surgical Bx 2. Thoracoscopic Bx 3. Bronchoscopic BX

Case 12

Case12 : Question 12.1 What is the main pattern of this HRCT? 1. Interlobular line 2. Intralobular line 3. GGO

Case 12 : Question 12.2 What is the axial distribution? 1. Peripheral 2. Central 3. Diffuse

Case 12 : Question 12.3 What is the intralobular distribution? 1. Perilobular 2. Centrilobular 3. Panlobular

Case 13

Case 13 : Question 13.1 What about the lung volume? 1. Increase 2. Normal 3. Decrease

Case 13 : Question 13.2 What is the main pattern of this HRCT? 1. Reticulation 2. Nodule 3. Honeycombing

Case 13 : Question 13.3 What is the craniocaudal distribution? 1. Upper 2. Diffuse 3. Lower

Case 13 : Question 13.4 What is the axial distribution? 1. Peripheral 2. Diffuse 3. Central

Case 13 : Question 13.5 What is the intralobular distribution? 1. Perilobular 2. Centrilobular 3. Panlobular

Case 14

Case 14 : Question 14.1 What is the main pattern of this HRCT? 1. Reticulation 2. Groundglass opacity 3. Honeycombing

Case 14 : Question 14.2 What is the craniocaudal distribution? 1. Upper 2. Diffuse 3. Lower

Case 14 : Question 14.3 What is the axial distribution? 1. Peripheral 2. Diffuse 3. Central

Case 14 : Question 14.4 What is the intralobular distribution? 1. Panlobular 2. Centrilobular 3. Perilobular

Case 14 : Question 14.5 A patient known to have systemic sclerosis for 5 years develops dry cough, dyspnea on exertion and shortness of breath. What is the proper management? 1. Surgical biopsy 2. Pulmonary function test 3. Bronchoscopic biopsy

Case 15

Case 15 : Question 15.1 What is the main pattern of this HRCT? 1. Groundglass opacity 2. Nodule 3. Reticulation

Case 15 : Question 15.2 What is the most likely diagnosis? 1. BOOP 2. Lymphoma 3. NSIP

Case 15 : Question 15.3 What is the best further management? 1. Bronchoscopic biopsy 2. Surgical biopsy 3. Steroid

Case 16

Case 16: Question 16.1 What is the main pattern of this HRCT? 1. Groundglass opacity 2. Nodule 3. reticulation

Case 16: Question 16.2 What is the craniocaudal distribution? 1. Upper 2. Diffuse 3. Lower

Case 16 : Question 16.3 What is the axial distribution? 1. Peripheral 2. Diffuse 3. Central

Case 17

Case 17 : Question 17.1 What about the lung volume? 1. Increased 2. Normal 3. Decreased

Case 17 : Question 17.2 What is the axial distribution? 1. Peripheral 2. Diffuse 3. Central

Case 17 : Question 17.3 What is the intralobular distribution? 1. Perilymphatic 2. Centrilobular 3. Random

Case 18

Case 18 : Question 18.1 What is the main pattern of this HRCT? 1. Ground glass opacity 2. Septal thickening 3. 1 and 2

Case 18: Question 18.2 What is the craniocaudal distribution? 1. Upper 2. Diffuse 3. Lower

Case 18: Question 18.3 What is the axial distribution? 1. Peripheral 2. Diffuse 3. Central

Case 18 : Question 18.4 What is intralobular distribution? 1. Perilymphatic 2. Centrilobular 3. Random

Case 18 : Question 18.5 What is the associated finding? 1. Lymph node enlargement 2. Lung mass 3. Pleural thickening

Case 18 : Question 18.6 What is the diagnosis? 1. Lymphangitic carcinomatosis 2. Pulmonary alveolar proteinosis 3. Pulmonary edema

Case 19

Case 19 : Question 19.1 What is the main pattern of this HRCT? 1. Ground glass opacity 2. Ill-defined nodule 3. 1. and 2.

Case 19: Question 19.2 What is the axial distribution? 1. Peripheral 2. Diffuse 3. Central

Case 19 : Question 19.3 What is the intralobular distribution? 1. Perilymphatic 2. Centrilobular 3. Random

Case 19 : Question 19.4 What is the diagnosis? 1. Hypersensitivity pneumonitis 2. NSIP 3. PAP

Case 20

Case 20 : Question 20.1 What is the main pattern of this HRCT? 1. Nodule 2. Ground glass opacity 3. Septal thickening 4. 2 and 3.

Case 20 : Question 20.2 What is the distribution of this HRCT in axial view? 1. Peripheral 2. Diffuse 3. Central

Case 20 : Question 20.3 What is the intralobular distribution? 1. Perilymphatic 2. Centrilobular 3. Random

Case 20: Question 20.4 What is the associated finding? 1. Lymph node enlargement 2. Pericardial thickening 3. 1. and 2.

Case 20: Question 20.5 What is the diagnosis? 1. Lymphangitic carcinomatosis 2. PAP 3. Pulmonary edema

Suspected diffused lung disease Chest radiograph Normal or equivocal Abnormal Suggestive of sarcoidosis HRCT with prone views HRCT Trans bronchial Bx Normal Abnormal See next slide Bx if clinical/physiologic evidence of disease See next slide

Suspected diffused lung disease Specific CT pattern(uip,eg,lam,h P, Lipoid Pneumonia) CT pattern suggestive of HP sarcoid, lymphagitic carcinoma,pap, alveolar carcinoma,eosinophillic pneumonia, BOOP Other CT pattern Accept CT diagnosis if clinical scenario is consistent Trans bronchial biopsy and/or brochoalveolar lavage (CT directed) Thoracosopic biopsy (CT directed)

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