Interstitial lung disease: Difference between revisions
From IDWiki
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** Exposures |
** Exposures |
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*** [[Hypersensitivity pneumonitis]] |
*** [[Hypersensitivity pneumonitis]] |
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| − | *** Inorganic |
+ | *** Inorganic: [[silicosis]] and [[asbestosis]] |
| − | **** Silica |
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| − | **** Asbestos |
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*** Drugs |
*** Drugs |
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**** [[Nitrofurantoin]] |
**** [[Nitrofurantoin]] |
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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]] |
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Revision as of 11:52, 18 February 2023
Differential Diagnosis
- Primary
- Secondary
- Inflammatory or connective tissue diseases
- Exposures
- Hypersensitivity pneumonitis
- Inorganic: silicosis and asbestosis
- Drugs
- Nitrofurantoin
- Chemotherapy
- Cyclophosphamide
- Others
- Methotrexate
- Organic
- Occupational and hobby lung diseases
- 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)
