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A heterogenous group diffuse inflammatory
disorders that affect the alveoli and septal
interstitium of the lower respiratory tract of
the lung.
Causes of interstitial lung diseases :
 Idiopathic pulmonary fibrosis
 • It is called cryptogenic fibrosing alveolitis or
   Hamman – rich syndrome
 • The cause is unknown but the disease
   represents the inflammatory and immune
   response of the lung to the tissue damage


 Collagenic vascular diseases
 • Rheumatoid arthritis, systemic sclerosis or
   ankylosing spondylitis
 • Dermatomyositis,    polymyositis    or    mixed
   connective tissue diseases
Occupational lung diseases
 • Inhalation of organic dusts “extrinsic allergic
   alveolitis” : as Baggosis
 • Inhalation   of      inorganic         dusts      “
   Pneumoconiosis” : as Asbestosis
  Malignancy
 • Bronchoalveolar      carcinoma   and   lymphangitis
   carcinomatosis
 • Leukaemias and lymphomas
  Infectious diseases
• Miliary tuberculosis, viral and atypical pneumonias
Medications
• Methotrexate, Azathioprine and bleomycin
• Sulphonamides, Aminodarone and insecticides
Miscellaneous
• Ulcerative colitis, chronic active hepatitis
• Alveolar proteinosis and microlithiasis
• Hashimoto’s     thyroiditis   and   Goodpasture’s
  syndrome
Pathological types
• Mural types
• Desquamative type
• Lymphocytic type
Symptoms :
 Onset
* It usually insidious and gradually progressive
* It may be acute with rapidly progressive course
“in
  Hamman rich syndrome”
* It may      be   subacute   “in   extrinsic   allergic
alveolitis”
 Symptoms
* Dry cough
* Gradual progressive dyspnea appearearly on
Sign :

    General signs
    • Clubbing
    • Cyanosis that appears early on exertion but
      later at rest


    Local sign
•      Crackles
•      Rhonchi
Radiological investigations :
  Chest x-ray

• Diffuse bilateral reticulonodular pattern through
  both lung fields
• It is more pronounced at the lower lung zone
• Honey comb appearance
• Homogenous opacity
• Multiple shadows of equal size scattered all over
  lung in milliary TB
• Features of complications    : Right ventricular
  enlargement , Pulmonary hypertension
reticulonodular infiltrates
distortion of the lung architecture and traction bronchiectasis
 HRCT ( High Resolution CT scan )
 Ventilation – Perfusion scan
Blood test : leucocyte
Other tests : bronchoscopy, lung biopsy, etc.
Specific Treatment :

  Steroid “Prednisone”


Other lines of treatment :
 Symptomatic treatment as : oxygen inhalation and
antitussive
  • Supportive treatment as : good nutrition and
    vitamins
  • Treatment    of   the    cause   :   as   pulmonary
    infections
  • Treatment of complications as
Symptomatic treatment as : oxygen inhalation and
 antitussive
• Supportive treatment as : good nutrition and
  vitamins
• Treatment    of   the   cause   :   as   pulmonary
  infections
• Treatment of complications as
 - Pulmonary hypertension and corpulmonale
Interstitial lung disease

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Interstitial lung disease

  • 1.
  • 2. A heterogenous group diffuse inflammatory disorders that affect the alveoli and septal interstitium of the lower respiratory tract of the lung.
  • 3. Causes of interstitial lung diseases : Idiopathic pulmonary fibrosis • It is called cryptogenic fibrosing alveolitis or Hamman – rich syndrome • The cause is unknown but the disease represents the inflammatory and immune response of the lung to the tissue damage Collagenic vascular diseases • Rheumatoid arthritis, systemic sclerosis or ankylosing spondylitis • Dermatomyositis, polymyositis or mixed connective tissue diseases
  • 4. Occupational lung diseases • Inhalation of organic dusts “extrinsic allergic alveolitis” : as Baggosis • Inhalation of inorganic dusts “ Pneumoconiosis” : as Asbestosis Malignancy • Bronchoalveolar carcinoma and lymphangitis carcinomatosis • Leukaemias and lymphomas Infectious diseases • Miliary tuberculosis, viral and atypical pneumonias
  • 5. Medications • Methotrexate, Azathioprine and bleomycin • Sulphonamides, Aminodarone and insecticides Miscellaneous • Ulcerative colitis, chronic active hepatitis • Alveolar proteinosis and microlithiasis • Hashimoto’s thyroiditis and Goodpasture’s syndrome
  • 6. Pathological types • Mural types • Desquamative type • Lymphocytic type
  • 7. Symptoms : Onset * It usually insidious and gradually progressive * It may be acute with rapidly progressive course “in Hamman rich syndrome” * It may be subacute “in extrinsic allergic alveolitis” Symptoms * Dry cough * Gradual progressive dyspnea appearearly on
  • 8. Sign : General signs • Clubbing • Cyanosis that appears early on exertion but later at rest Local sign • Crackles • Rhonchi
  • 9. Radiological investigations : Chest x-ray • Diffuse bilateral reticulonodular pattern through both lung fields • It is more pronounced at the lower lung zone • Honey comb appearance • Homogenous opacity • Multiple shadows of equal size scattered all over lung in milliary TB • Features of complications : Right ventricular enlargement , Pulmonary hypertension
  • 11. distortion of the lung architecture and traction bronchiectasis
  • 12.  HRCT ( High Resolution CT scan )  Ventilation – Perfusion scan Blood test : leucocyte Other tests : bronchoscopy, lung biopsy, etc.
  • 13. Specific Treatment : Steroid “Prednisone” Other lines of treatment : Symptomatic treatment as : oxygen inhalation and antitussive • Supportive treatment as : good nutrition and vitamins • Treatment of the cause : as pulmonary infections • Treatment of complications as
  • 14. Symptomatic treatment as : oxygen inhalation and antitussive • Supportive treatment as : good nutrition and vitamins • Treatment of the cause : as pulmonary infections • Treatment of complications as - Pulmonary hypertension and corpulmonale