2. a. Reticular Interstitial Pattern
b. Ground Glass Pattern
c. Nodular Pattern
d. Cystic Pattern
e. Mosaic Pattern
3. Reticular pattern
• Linear shadows (multiple lines) appearing as mesh or net
• Can appear as
Per bronchial cuffing
Septal thickening
Traction bronchiectasis
Honey comping
20. Nodular pattern
• Multiple rounded opacities 1-10 mm(miliary = 1-2 mm)
• In most cases small nodules can be placed into one of three
categories(PCR):
– Randomly distributed
– Centrilobular distribution
– Perilymphatic distribution
28. Hypersensitivity pneumonitis
• Immunologic response
• Can be normal
• Acute; consolidation
• Subacute; centrilobular ill defined nodules surrounded by
areas of ground glass attenuation
32. • Miliary pneumoconiosis
– Inhalation of inorganic dust particles that overwhelm the
normal clearance mechanism of the respiratory tract
• Silica - Silicosis
• Coal workers' pneumoconiosis(CWP)
Simple; Nodules
Complicated; Progressive Massive Fibrosis
33. Nodules:
• Dense multiple nodules
sparing the base
• Calcification may occur
34.
35. complicated
Progressive Massive Fibrosis:
• Nodules enlarge and coalesce to form two big masses on
either side of the lungs
• Bilateral areas of confluent fibrosis; almost symmetrical,
almost always in the upper half of the lung – almost
pathognomonic
• Egg shell calcification of lymph nodes
41. Pulmonary Alveolar Microlithiasis:
• idiopathic
• bilateral sand like calcification
• middle to lower zone predilection
• Black pleura sign; at their interface with the chest wall
42.
43. • Nearly uniform distribution of
typical fine, sandlike mottling in
the lungs
• The tangential shadow of the
pleura is displayed along the
lateral wall of the chest as a
dark lucent strip (arrows)
44. Differential Diagnosis of multiple small(pin point)
micronodules:
Silicosis
Stannosis (inhalation of tin oxide)
Barytosis (inhalation of barytes)
Limestone & marble workers
Alveolar microlithiasis
45. Cystic pattern
– Radiolucent areas with a wall thickness of less than 4mm
– Multiple thin walled air containing lesions 1cm or
more(not seen by x-rays except for bronchiectasis)
46.
47.
48. • Causes may be are:
– Lymphangioleiomyomatosis(LAM)
– Langerhan’s Cell Histiocytosis(LCH)
– Emphysema
– Cystic Bronchiectasis
49. LAM
It almost exclusively affects women of child bearing age
– Numerous cystic spaces – 90%
– Size of cysts usually 5 to 10mm
– Thin walled
– Surrounded by normal lung
– Recurrent pneumothorax – 70%
– Chylous pleural effusions – 25%
– Proliferation of smooth muscles in the walls of alveoli, bronchi,
vessels and pleural causing air trapping
50.
51. LCH
– Granulomatous disease
– Eosinophilic granuloma of lung
– Smoking
– Extrapulmonary; lytic rib or vertebral lesions
52. • Radiographic features:
– Small irregular cystic spaces in lung parenchyma (spares the lower
lung zones)
– 3 to 10 mm pulmonary nodules
– Pneumothorax – 30%
57. Cystic Bronchiectasis:
• Cystic structures continuous with the bronchial tree –
cysts along the distribution of the bronchi
• More in the lower lobes
• Peripheral cysts
58.
59.
60. Mosaic pattern
• Used to describe density differences between affected
and unaffected lung areas, there are patchy areas of
black and white lung
• It is a non-specific finding
• Causes may be are:
Obstructive Small Airway Disease
Occlusive Vascular Diseases
Parenchymal( infiltrating) Disease
61. Obstructive Small Airway Disease:
• Low attenuation regions are abnormal and reflect decreased
perfusion of the poorly ventilated regions
Eg. Bronchiectasis, cystic fibrosis, constrictive bronchiolitis
Occlusive Vascular Disease:
• Can be termed a mosaic perfusion pattern in this setting, low
attenuation regions are abnormal and reflect relative oligemia
Eg. Chronic pulmonary embolism
Parenchymal Disease:
• High attenuation regions are abnormal and represent ground-
glass opacity