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INTERSTITIAL LUNG DISEASES
by Dr. Henock.N, Radiology resident
AYDER HOSPITAL
a. Reticular Interstitial Pattern
b. Ground Glass Pattern
c. Nodular Pattern
d. Cystic Pattern
e. Mosaic Pattern
Reticular pattern
• Linear shadows (multiple lines) appearing as mesh or net
• Can appear as
 Per bronchial cuffing
 Septal thickening
 Traction bronchiectasis
 Honey comping
Ethiology
 Idiopatic interstitial pneumonia
• UIP COP
• NSIP RB-ILD
• DIP LIP
 IPE
 + Adenopathy
• Sarcoidosis
• Lymphangitic carcinomatosis
UIP
Reticular opacities ( mainly basal )
Traction bronchiectasis
Honeycombing ; peripheral and sub pleural, many layers
uip
 NSIP
Reticular opacity; symmetric
Ground glass opacity
Scattered micro nodules
Advanced; - traction bronchiectasis
- consolidation
-microcytic
nsip
 COP
consolidation and ground glass opacity
- Per bronchial or peripheral
- Lower lobe predominance
N.B; sub pleural is usually spared
cop
 RB-ILD & DIP
 smoking related
 Ground glass opacities + centrilobular nodules
Upper lobe predominant- RB-ILD
Lower lobe predominant- DIP
RB-ILD
• LIP
 Usually associated with hiv and sjogren syndrome
 Ground glass opacity + perivascular cysts
LIP
With adenopathy
 SARCOIDOSIS
 laps
 Reticulonodular opacities
 Predominantly upper and middle lobes
sarcoidosis
 lymphangitic carcinomatosis
 laps
 Irregular interlobular septal thickening
 Pleural effusion
LC
 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
 Random distribution
 Centrilobular distribution:
 Perilymphatic distribution
• Causes of miliary
pulmonary nodules
– Miliary TB
– Fungal Infection
– Miliary metastases
– Pneumoconiosis
– Wegner’s Granulomatosis
– Pulmonary Alveolar
Microlithiasis
 Miliary PTB
Soft pulmonary micronodules(uniform in size &
distribution, 1-3mm) scattered through out both
lung fields with no calcification
• Fungal miliary pulmonary micronodular pattern
– Endemic human mycoses(in certain geographic areas)
• Histoplasmosis
• Coccidioidomycosis
• Blastomycosis
– Opportunistic mycoses(worldwide in distribution)
• Invasive aspergillosis
• Cryptococosis
• Candidiasis
• Mucormycosis
Hypersensitivity pneumonitis
• Immunologic response
• Can be normal
• Acute; consolidation
• Subacute; centrilobular ill defined nodules surrounded by
areas of ground glass attenuation
• Metastatic miliary pulmonary micronodular pattern
– Thyroid carcinoma
– Renal cell carcinoma
– Breast carcinoma
– Malignant melanoma
– Pancreatic neoplasms
– Osteosarcoma
– Trophoblastic disease
• 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
 Nodules:
• Dense multiple nodules
sparing the base
• Calcification may occur
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
• Wegner’s granulomatosis
– Necrotizing autoimmune disorder
– Lung, sinonasal , renal
– multiple nodules with cavitation(common)
Pulmonary Alveolar Microlithiasis:
• idiopathic
• bilateral sand like calcification
• middle to lower zone predilection
• Black pleura sign; at their interface with the chest wall
• 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)
 Differential Diagnosis of multiple small(pin point)
micronodules:
Silicosis
Stannosis (inhalation of tin oxide)
Barytosis (inhalation of barytes)
Limestone & marble workers
Alveolar microlithiasis
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)
• Causes may be are:
– Lymphangioleiomyomatosis(LAM)
– Langerhan’s Cell Histiocytosis(LCH)
– Emphysema
– Cystic Bronchiectasis
 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
 LCH
– Granulomatous disease
– Eosinophilic granuloma of lung
– Smoking
– Extrapulmonary; lytic rib or vertebral lesions
• Radiographic features:
– Small irregular cystic spaces in lung parenchyma (spares the lower
lung zones)
– 3 to 10 mm pulmonary nodules
– Pneumothorax – 30%
• Emphysema
– Centrilobular
– Paraseptal
– Panlobular
– Bullous
Cystic Bronchiectasis:
• Cystic structures continuous with the bronchial tree –
cysts along the distribution of the bronchi
• More in the lower lobes
• Peripheral cysts
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
 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
References
 Fundamentals of diagnostic radiology, 4th edition
 Thoracic imaging, pulmonary & cardiovascular radiology;
 Chest radiology, the essentials, 2nd edition
 Classification of diffuse lung diseases , Radiographics 2013
 HRCT diffuse cystic and mosaic pattern, AJR 2013
Interstitial lung disease Radiology

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Interstitial lung disease Radiology

  • 1. INTERSTITIAL LUNG DISEASES by Dr. Henock.N, Radiology resident AYDER HOSPITAL
  • 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
  • 4.
  • 5. Ethiology  Idiopatic interstitial pneumonia • UIP COP • NSIP RB-ILD • DIP LIP  IPE  + Adenopathy • Sarcoidosis • Lymphangitic carcinomatosis
  • 6. UIP Reticular opacities ( mainly basal ) Traction bronchiectasis Honeycombing ; peripheral and sub pleural, many layers
  • 7. uip
  • 8.  NSIP Reticular opacity; symmetric Ground glass opacity Scattered micro nodules Advanced; - traction bronchiectasis - consolidation -microcytic
  • 10.  COP consolidation and ground glass opacity - Per bronchial or peripheral - Lower lobe predominance N.B; sub pleural is usually spared
  • 11. cop
  • 12.  RB-ILD & DIP  smoking related  Ground glass opacities + centrilobular nodules Upper lobe predominant- RB-ILD Lower lobe predominant- DIP
  • 14. • LIP  Usually associated with hiv and sjogren syndrome  Ground glass opacity + perivascular cysts
  • 15. LIP
  • 16. With adenopathy  SARCOIDOSIS  laps  Reticulonodular opacities  Predominantly upper and middle lobes
  • 18.  lymphangitic carcinomatosis  laps  Irregular interlobular septal thickening  Pleural effusion
  • 19. LC
  • 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
  • 21.  Random distribution  Centrilobular distribution:  Perilymphatic distribution
  • 22.
  • 23. • Causes of miliary pulmonary nodules – Miliary TB – Fungal Infection – Miliary metastases – Pneumoconiosis – Wegner’s Granulomatosis – Pulmonary Alveolar Microlithiasis
  • 24.  Miliary PTB Soft pulmonary micronodules(uniform in size & distribution, 1-3mm) scattered through out both lung fields with no calcification
  • 25.
  • 26.
  • 27. • Fungal miliary pulmonary micronodular pattern – Endemic human mycoses(in certain geographic areas) • Histoplasmosis • Coccidioidomycosis • Blastomycosis – Opportunistic mycoses(worldwide in distribution) • Invasive aspergillosis • Cryptococosis • Candidiasis • Mucormycosis
  • 28. Hypersensitivity pneumonitis • Immunologic response • Can be normal • Acute; consolidation • Subacute; centrilobular ill defined nodules surrounded by areas of ground glass attenuation
  • 29.
  • 30. • Metastatic miliary pulmonary micronodular pattern – Thyroid carcinoma – Renal cell carcinoma – Breast carcinoma – Malignant melanoma – Pancreatic neoplasms – Osteosarcoma – Trophoblastic disease
  • 31.
  • 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
  • 36.
  • 37.
  • 38.
  • 39. • Wegner’s granulomatosis – Necrotizing autoimmune disorder – Lung, sinonasal , renal – multiple nodules with cavitation(common)
  • 40.
  • 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%
  • 53.
  • 54. • Emphysema – Centrilobular – Paraseptal – Panlobular – Bullous
  • 55.
  • 56.
  • 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
  • 62.
  • 63.
  • 64. References  Fundamentals of diagnostic radiology, 4th edition  Thoracic imaging, pulmonary & cardiovascular radiology;  Chest radiology, the essentials, 2nd edition  Classification of diffuse lung diseases , Radiographics 2013  HRCT diffuse cystic and mosaic pattern, AJR 2013