Interstitial lung disease: Difference between revisions
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* Primary |
* Primary |
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** IPF |
** [[IPF]] |
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** COP |
** [[COP]] |
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** NSIP |
** [[NSIP]] |
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* Secondary |
* Secondary |
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** Inflammatory or connective tissue diseases |
** Inflammatory or connective tissue diseases |
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*** Rheumatoid arthritis |
*** [[Rheumatoid arthritis]] |
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*** Systemic lupus erythematosus |
*** [[Systemic lupus erythematosus]] |
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*** Dermatomyositis |
*** [[Dermatomyositis]] |
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*** Systemic sclerosis |
*** [[Systemic sclerosis]] |
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*** Sarcoidosis |
*** [[Sarcoidosis]] |
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** Exposures |
** Exposures |
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*** Hypersensitivity pneumonitis |
*** [[Hypersensitivity pneumonitis]] |
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*** Drugs: [[nitrofurantoin]], chemotherapy ([[cyclophosphamide]], [[bleomycin]]), [[methotrexate]], [[amiodarone]] |
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*** Inorganic |
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*** Inorganic exposures: [[silicosis]] and [[asbestosis]] |
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**** Silica |
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**** Asbestos |
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**** [[Hypersensitivity pneumonitis]], including bird fancier's lung, cheese-washer's lung, farmer's lung |
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*** Drugs |
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**** [[ |
**** Hot tub lung ([[Mycobacterium avium]]) |
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⚫ | |||
**** Chemotherapy |
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***** Cyclophosphamide |
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***** Others |
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**** Methotrexate |
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*** Organic |
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* Mimickers |
* Mimickers |
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** Congestive heart failure |
** [[Congestive heart failure]] |
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** Interstitial infections |
** Interstitial infections |
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*** [[Pneumocystis jirovecii pneumonia]] |
*** [[Pneumocystis jirovecii pneumonia]] |
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*** [[Legionella]] |
*** [[Legionella]] |
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*** Viral pneumonia |
*** Viral pneumonia |
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** Lymphangitic carcinomatosis |
** [[Lymphangitic carcinomatosis]] |
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=== By Location Predominance === |
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==== Upper Lobe Predominance (HASTEN) ==== |
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* [[Hypersensitivity pneumonitis]] |
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* [[Ankylosing spondylitis]] |
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* [[Sarcoidosis]] and [[silicosis]] |
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* [[Tuberculosis]], viral pneumonia, [[Mycoplasma]] |
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* Eosinophilic granulomas (aka pulmonary [[Langerhan cell histiocytosis]], present with spontaneous pneumothorax) |
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* [[Neurofibromatosis]] |
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==== Lower Lobe Predominance (BAD RASH) ==== |
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* [[Bleomycin]] |
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* [[Amiodarone]] |
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* Drugs: [[nitrofurantoin]], [[cyclophosphamide]], [[methotrexate]] |
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* [[Rheumatoid lung]] |
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* [[Asbestosis]] |
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* [[Scleroderma]] |
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* [[Hamman-Rich syndrome]] (aka [[acute interstitial pneumonia]] = rare, fulminant form of IPF) |
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[[Category:Respirology]] |
[[Category:Respirology]] |
Latest revision as of 15:56, 18 February 2023
Differential Diagnosis
- Primary
- Secondary
- Inflammatory or connective tissue diseases
- Exposures
- Hypersensitivity pneumonitis
- Drugs: nitrofurantoin, chemotherapy (cyclophosphamide, bleomycin), methotrexate, amiodarone
- Inorganic exposures: silicosis and asbestosis
- Occupational and hobby exposures
- Hypersensitivity pneumonitis, including bird fancier's lung, cheese-washer's lung, farmer's lung
- Hot tub lung (Mycobacterium avium)
- Radiation pneumonitis
- Mimickers
- Congestive heart failure
- Interstitial infections
- Pneumocystis jirovecii pneumonia
- Mycoplasma
- Legionella
- Viral pneumonia
- Lymphangitic carcinomatosis
By Location Predominance
Upper Lobe Predominance (HASTEN)
- Hypersensitivity pneumonitis
- Ankylosing spondylitis
- Sarcoidosis and silicosis
- Tuberculosis, viral pneumonia, Mycoplasma
- Eosinophilic granulomas (aka pulmonary Langerhan cell histiocytosis, present with spontaneous pneumothorax)
- Neurofibromatosis
Lower Lobe Predominance (BAD RASH)
- Bleomycin
- Amiodarone
- Drugs: nitrofurantoin, cyclophosphamide, methotrexate
- Rheumatoid lung
- Asbestosis
- Scleroderma
- Hamman-Rich syndrome (aka acute interstitial pneumonia = rare, fulminant form of IPF)