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“Crazy-Paving” Pattern at Thin-
   Section CT of the Lungs:
 RadioGraphics 2003; 23:1509-1519
Introduction
Reported in infectious, neoplastic, idiopathic, inhalational,
and sanguineous disorder of the lungs
Characterized by scattered or diffuse ground-glass
attenuation with superimposed interlobular septal
thickening and intralobular lines
Infection
• Pneumocystis carinii pneumonia (PCP)




Neoplasm
• Mucinous Bronchioalveolar Carcinoma (BAC)




Idiopathic Disorders
• Pulmonary Alveolar Proteinosis (PAP)
• Sarcoidosis



Inhalation Disorders
• Lipoid Pneumonia




Sanguineous Disorders
• Adult Respiratory Distress Syndrome (ARDS)
• Pulmonary Hemorrhage Syndromes
eoplasm
Mucinous Bronchioalveolar Carcinoma (BAC)




 iopathic Disorders
 ulmonary Alveolar Proteinosis (PAP)
 arcoidosis



 halation Disorders
 ipoid Pneumonia
Pneumocystis Carinii
• Symptoms: cough, dyspnea, low-grade fever
• Chest Radiograph:
   – Bilateral, perihilar reticular and poorly defined ground-glass
      opacities  alveolar consolidation
   – Scattered ground-glass attenuation (interlobular septal
      thickening)
• Histology: foamy nature of the alveolar exudates and thickening of
  the alveolar wa&s by edema and ce&ular infiltrates
Mucinous Bronchioalveolar Carcinoma
              (BAC)

  Mucinous  mucin-producing columnar ce&s with
  moderate nuclear atypia
  Lepidic growth pattern through the airways and air spaces
  with preservation of the lung architecture.
  Symptoms: Bronchorrhea
Mucinous Bronchioalveolar Carcinoma
              (BAC)

  Chest Radiography:
    i&-defined consolidation or ground-glass opacities occur
    in a focal or multilobar distribution
    Lymphadenopathy
    Pleural effusion
  Chest HRCT:
    Numerous and alveolar consolidation and ground-glass
    attenuation  crazy-paving pattern
Pulmonary Alveolar
Fi&ing of the alveoli by a proteinaceous material
Associated with an inflammatory response in the adjacent
interstitium
Most common in adults, 20-50 years old
Dyspnea and nonproductive cough
Less common: Pleuritic chest pain, malaise, low-grade fever
Pulmonary Alveolar
Radiography : bilateral, symmetric alveolar consolidation or
ground-glass opacity, particularly in perihilar or hilar
distribution ~ pulmonary edema
HRCT : diffuse ground-glass attenuation with superimposed
intra- and interlobular septal thickening
Diagnosis with bronchoalveolar lavage
Sarcoidosis
Development of noncaseating granulomatous inflammation
Parenchymal findings: irregular thickening of the
bronchovascular bundles and sma& nodules along vessels
Nonspecific Interstitial
Interstitial inflammation and fibrosis with temporal and
spatial uniformity
Does not fulfi& clinicopathologic criteria for usual
interstitial pneumonia, desquamative interstitial
pneumonia, or acute interstitial pneumonia
Chest Radiography: bilateral pulmonary opacities, mainly
localized in the middle and lower zones
Nonspecific Interstitial
Chest CT findings: ground-glass attenuation, bilateral and
symmetric with a tendency to subpleural and basal
predominance
Other findings: Consolidation and irregular reticular lines
superimposed on a background of ground-glass attenuation
Honeycombing is typica&y absent
Organizing Pneumonia
Past: bronchiolitis obliterans organizing pneumonia
Chronic inflammatory process characterized by focal plugs of
granulation tissue (Masson bodies) in the lumina of distal sma&
airways
Associated with intraalveolar foamy macrophages and interstitial
ce&ular response
Most cases are idiopathic (cyrptogenic organizing pneumonia)
Organizing Pneumonia
Associated with co&agen-vascular diseases, infection, and
toxic effect drugs (bleomycin, methotrexate,
cyclophosphamide, gold salts, topotecan, amiodarone)
Symptoms: cough, dyspnea, fever of several weeks, and
leukocytosis
Response to steroid therapy
Organizing Pneumonia
Radiography and CT: scattered and asymmetric
consolidation bilatera&y, and peripheral (> 50%)
Organizing Pneumonia
HRCT: subpleural and peribronchovascular consolidation,
crazy-paving pattern is uncommon
Exogenous Lipoid
Pulmonary disorder resulting ,om chronic aspiration or
inhalation of animal, vegetable, or petroleum-based oils or
fats
Predisposing factors: structural abnormalities, neurologic
defects, and chronic i&ness
Histopathologic: intraalveolar macrophages containing
abundant cytoplasmic lipoproteinaceous material within
‘normal’ alveoli
Exogenous Lipoid
Subacute manifestations: larger vacuoles within alveoli,
surrounded by macrophages, inflammatory infiltrates of
alveolar wa&s and interlobular septa
Risk factors: repeated episodes of aspiration
Symptoms: mild ever, shortness of breath, and chest
discomfort
Exogenous Lipoid
Chest radiograph: nonspecific, bilateral lower-lobe airspace
opacities, mixed alveolar and interstitial opacities, and
poorly marginated focal mass-like lesions mimic pulmonary
neoplasm
Exogenous Lipoid Pneumonia
   Lipoid Pneumonia
HRCT:
  consolidation characterized by low attenuation (-35 to -75
  HU) lipid deposition
  Geographic ground-glass attenuation associated with
  interlobular septal thickening within areas of ground-
  glass attenuation
Intraalveolar and interstitial accumulation of lipid-laden
macrophages and hyperplasia of tyoe II pneumatocytes in
Exogenous Lipoid
Diagnosis: Bronchoalveolar lavage, transbronchial biopsy,
or open lung biopsy combined with history of ingestion and
radiographic studies.
Adult Respiratory Distress Syndrome
              (ARDS)

 Pulmonary edema characterized by re,actory hypoxemia
 and respiratory distress
 Risk Factors: Shock, contusion, infection, sepsis, aspiration,
 drug abuse, and inhalation of noxious substances
 Diagnosis: impaired diffusion capacity (DLCO), reduced
 compliance of the lung, and typical radiologic findings
Adult Respiratory Distress Syndrome
              (ARDS)

 Chest Radiography:
   Bilateral homogenous pulmonary opacities
   Cardiomegaly and upper-lobe diversion are usua&y
   absent
 Chest HRCT:
   Bilateral consolidation and ground-glass attenuation
   Reticular and linear attenuation
Adult Respiratory Distress Syndrome
              (ARDS)

 May progress to architectural distortion, consolidation with
 bronchiectasis, and honeycombing
 Histologic: Edema of the alveoli and perivascular spaces
 with fi&ing of the alveoli by a protein rich fluid
Pulmonary Hemorrhage Syndromes

  Wide spectrum of diseases:
    Idiopathic pulmonary hemosiderosis
    Wegener granulomatosis
    Churg-Strauss syndrome
    Goodpasture syndrome
    Co&agen-vascular disease (SLE)
    Drug-induced coagulopathy
    Hemorrhage associated with malignancy
Pulmonary Hemorrhage Syndromes

Diffuse parenchymal bleeding:
  Hemodynamic modification of capi&ary pulmonary blood
  flow
  Pathologic changes in the alveolar wa&
Symptoms: hemoptysis, dyspnea, and anemia
Diagnosis: Bronchoalveolar lavage or Fe content of alveolar
macrophages
Pulmonary Hemorrhage Syndromes
Occurs up to 2% patients with SLE, associated with
extrapulmonary manifestations like glomerulonephritis
42 to 66 % patients do not have hemoptysis
Chest Radiograph and HRCT: asymmetric acinar and ground-glass
opacities or attenuation and crazy-paving pattern
Conclusions
Crazy-paving pattern: scattered or diffuse ground-glass
opacities or attenuation with superimposed
interlobular septal thickening and intralobular lines
Limited differential diagnosis  CT manifestations
of many diverse entities
Knowledge of the etiology prevent diagnostic errors
Location of characteristics, additional radiologic
findings, history and clinical presentation can o-en be
useful in su.esting the appropriate diagnosis

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crazy paving pattern

  • 1. “Crazy-Paving” Pattern at Thin- Section CT of the Lungs: RadioGraphics 2003; 23:1509-1519
  • 2. Introduction Reported in infectious, neoplastic, idiopathic, inhalational, and sanguineous disorder of the lungs Characterized by scattered or diffuse ground-glass attenuation with superimposed interlobular septal thickening and intralobular lines
  • 3. Infection • Pneumocystis carinii pneumonia (PCP) Neoplasm • Mucinous Bronchioalveolar Carcinoma (BAC) Idiopathic Disorders • Pulmonary Alveolar Proteinosis (PAP) • Sarcoidosis Inhalation Disorders • Lipoid Pneumonia Sanguineous Disorders • Adult Respiratory Distress Syndrome (ARDS) • Pulmonary Hemorrhage Syndromes
  • 4. eoplasm Mucinous Bronchioalveolar Carcinoma (BAC) iopathic Disorders ulmonary Alveolar Proteinosis (PAP) arcoidosis halation Disorders ipoid Pneumonia
  • 5. Pneumocystis Carinii • Symptoms: cough, dyspnea, low-grade fever • Chest Radiograph: – Bilateral, perihilar reticular and poorly defined ground-glass opacities  alveolar consolidation – Scattered ground-glass attenuation (interlobular septal thickening) • Histology: foamy nature of the alveolar exudates and thickening of the alveolar wa&s by edema and ce&ular infiltrates
  • 6. Mucinous Bronchioalveolar Carcinoma (BAC) Mucinous  mucin-producing columnar ce&s with moderate nuclear atypia Lepidic growth pattern through the airways and air spaces with preservation of the lung architecture. Symptoms: Bronchorrhea
  • 7. Mucinous Bronchioalveolar Carcinoma (BAC) Chest Radiography: i&-defined consolidation or ground-glass opacities occur in a focal or multilobar distribution Lymphadenopathy Pleural effusion Chest HRCT: Numerous and alveolar consolidation and ground-glass attenuation  crazy-paving pattern
  • 8. Pulmonary Alveolar Fi&ing of the alveoli by a proteinaceous material Associated with an inflammatory response in the adjacent interstitium Most common in adults, 20-50 years old Dyspnea and nonproductive cough Less common: Pleuritic chest pain, malaise, low-grade fever
  • 9. Pulmonary Alveolar Radiography : bilateral, symmetric alveolar consolidation or ground-glass opacity, particularly in perihilar or hilar distribution ~ pulmonary edema HRCT : diffuse ground-glass attenuation with superimposed intra- and interlobular septal thickening Diagnosis with bronchoalveolar lavage
  • 10. Sarcoidosis Development of noncaseating granulomatous inflammation Parenchymal findings: irregular thickening of the bronchovascular bundles and sma& nodules along vessels
  • 11. Nonspecific Interstitial Interstitial inflammation and fibrosis with temporal and spatial uniformity Does not fulfi& clinicopathologic criteria for usual interstitial pneumonia, desquamative interstitial pneumonia, or acute interstitial pneumonia Chest Radiography: bilateral pulmonary opacities, mainly localized in the middle and lower zones
  • 12. Nonspecific Interstitial Chest CT findings: ground-glass attenuation, bilateral and symmetric with a tendency to subpleural and basal predominance Other findings: Consolidation and irregular reticular lines superimposed on a background of ground-glass attenuation Honeycombing is typica&y absent
  • 13. Organizing Pneumonia Past: bronchiolitis obliterans organizing pneumonia Chronic inflammatory process characterized by focal plugs of granulation tissue (Masson bodies) in the lumina of distal sma& airways Associated with intraalveolar foamy macrophages and interstitial ce&ular response Most cases are idiopathic (cyrptogenic organizing pneumonia)
  • 14. Organizing Pneumonia Associated with co&agen-vascular diseases, infection, and toxic effect drugs (bleomycin, methotrexate, cyclophosphamide, gold salts, topotecan, amiodarone) Symptoms: cough, dyspnea, fever of several weeks, and leukocytosis Response to steroid therapy
  • 15. Organizing Pneumonia Radiography and CT: scattered and asymmetric consolidation bilatera&y, and peripheral (> 50%)
  • 16. Organizing Pneumonia HRCT: subpleural and peribronchovascular consolidation, crazy-paving pattern is uncommon
  • 17. Exogenous Lipoid Pulmonary disorder resulting ,om chronic aspiration or inhalation of animal, vegetable, or petroleum-based oils or fats Predisposing factors: structural abnormalities, neurologic defects, and chronic i&ness Histopathologic: intraalveolar macrophages containing abundant cytoplasmic lipoproteinaceous material within ‘normal’ alveoli
  • 18. Exogenous Lipoid Subacute manifestations: larger vacuoles within alveoli, surrounded by macrophages, inflammatory infiltrates of alveolar wa&s and interlobular septa Risk factors: repeated episodes of aspiration Symptoms: mild ever, shortness of breath, and chest discomfort
  • 19. Exogenous Lipoid Chest radiograph: nonspecific, bilateral lower-lobe airspace opacities, mixed alveolar and interstitial opacities, and poorly marginated focal mass-like lesions mimic pulmonary neoplasm
  • 20. Exogenous Lipoid Pneumonia Lipoid Pneumonia HRCT: consolidation characterized by low attenuation (-35 to -75 HU) lipid deposition Geographic ground-glass attenuation associated with interlobular septal thickening within areas of ground- glass attenuation Intraalveolar and interstitial accumulation of lipid-laden macrophages and hyperplasia of tyoe II pneumatocytes in
  • 21. Exogenous Lipoid Diagnosis: Bronchoalveolar lavage, transbronchial biopsy, or open lung biopsy combined with history of ingestion and radiographic studies.
  • 22. Adult Respiratory Distress Syndrome (ARDS) Pulmonary edema characterized by re,actory hypoxemia and respiratory distress Risk Factors: Shock, contusion, infection, sepsis, aspiration, drug abuse, and inhalation of noxious substances Diagnosis: impaired diffusion capacity (DLCO), reduced compliance of the lung, and typical radiologic findings
  • 23. Adult Respiratory Distress Syndrome (ARDS) Chest Radiography: Bilateral homogenous pulmonary opacities Cardiomegaly and upper-lobe diversion are usua&y absent Chest HRCT: Bilateral consolidation and ground-glass attenuation Reticular and linear attenuation
  • 24. Adult Respiratory Distress Syndrome (ARDS) May progress to architectural distortion, consolidation with bronchiectasis, and honeycombing Histologic: Edema of the alveoli and perivascular spaces with fi&ing of the alveoli by a protein rich fluid
  • 25. Pulmonary Hemorrhage Syndromes Wide spectrum of diseases: Idiopathic pulmonary hemosiderosis Wegener granulomatosis Churg-Strauss syndrome Goodpasture syndrome Co&agen-vascular disease (SLE) Drug-induced coagulopathy Hemorrhage associated with malignancy
  • 26. Pulmonary Hemorrhage Syndromes Diffuse parenchymal bleeding: Hemodynamic modification of capi&ary pulmonary blood flow Pathologic changes in the alveolar wa& Symptoms: hemoptysis, dyspnea, and anemia Diagnosis: Bronchoalveolar lavage or Fe content of alveolar macrophages
  • 27. Pulmonary Hemorrhage Syndromes Occurs up to 2% patients with SLE, associated with extrapulmonary manifestations like glomerulonephritis 42 to 66 % patients do not have hemoptysis Chest Radiograph and HRCT: asymmetric acinar and ground-glass opacities or attenuation and crazy-paving pattern
  • 28. Conclusions Crazy-paving pattern: scattered or diffuse ground-glass opacities or attenuation with superimposed interlobular septal thickening and intralobular lines Limited differential diagnosis  CT manifestations of many diverse entities Knowledge of the etiology prevent diagnostic errors Location of characteristics, additional radiologic findings, history and clinical presentation can o-en be useful in su.esting the appropriate diagnosis

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