Interstitial lung disease: Difference between revisions
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==Classification== | ==Classification== | ||
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{{Family tree| | | | | | | | | | | | | | | A01 | | | | | | | | | | | | A01=Interstitial lung disease}} | |||
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{{Family tree| | | | | | | | | | B01 | | | | | | | | | | | | B02 | | | | | |B01=Lung Response:<br>Granulomatous|B02=Lung Response:<br>Alveolitis,<br>Interstitial Inflammation,<br>and Fibrosis }} | |||
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{{Family tree| | | | | | C01 | | | | | | C02 | | | | | | | | |!| | | | | | | | | | | |C01=Known|C02=Idiopathic (Unknown)}} | |||
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{{Family tree| | D01 | | D02 | | D03 | | D04 | | D05 | | D06 |!| | | | | | | | | | |D02=Inorganic dusts|D01=Hypersensitivity pneumonitis (organic dusts)|D03=Sarcoidosis||D04=Lymphomatoid granulomatosis|D05=Granulomatous vasculitides|D06=Bronchocentric granulomatosis}} | |||
{{Family tree| | | | |,|-|^|-|.| | | | | | | |,|-|^|-|.| | | |!| | | | | | | | | | |}} | |||
{{Family tree| | | | E01 | | E02 | | | | | | D07 | | D08 | | |!| | | | | | | | | | |E01=Beryllium|E02=Silica|D07=Eosinophilic granulomatosis with polyangiitis (Churg Strauss syndrome)|D08=Granulomatosis with polyangiitis (Wegener)}} | |||
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{{Family tree| | | | | | | | | | | | | | F01 | | | | | | | | F02 | | | | | | | | | | | | | | F01=Known cause|F02=Idiopathic (Unknown)}} | |||
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{{Family tree| G01 | | G06 | | G02 | | G03 | | G04 | | G05 | |!| | | | | | | | | | | | | | | | | | | G01=Drug-induced pulmonary toxicity|G06=Occupational and environmental exposure|G02=Radiation-induced lung injury|G03=Aspiration pneumonia|G05=Residual of acute respiratory distress syndrome|G04=Smoking-related}} | |||
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{{Family tree| I01 | | I02 | | I03 | | G07 | | G08 | | G09 | |!| | | | | | | | | | | | | | | | | | |I01=Inhaled inorganic dust|I02=Inhaled organic dusts|I03=Inhaled agents other than inorganic or organic dusts|G07=Desquamative interstitial pneumonia|G08=Respiratory bronchiolitis–associated interstitial lung disease|G09=Pulmonary Langerhans cell granulomatosis|}} | |||
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{{Family tree| H01 | | H07 | | H02 | | H08 | | H10 | | H09 | | H11 | | H06 | | H03 | | H04 | | H05 |H07=Idiopathic interstitial pneumonias|H01=Pulmonary alveolar proteinosis|H02=Lymphocytic infiltrative disorders<br>(lymphocytic interstitial pneumonitis<br>associated with connective tissue disease)|H08=Connective tissue<br>diseases|H03=Eosinophilic<br>pneumonias|H09=Inherited diseases|H04=Lymphangioleiomyomatosis|H10=Gastrointestinal or<br>liver diseases|H05=Amyloidosis|H11=Graft-versus-host disease|H06=Pulmonary hemorrhage syndromes}} | |||
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{{Family tree| |,|-|-|-|+|-|-|-|.| | | |!| | | |!| | | |!| | | |!| | | |!| | | | | | | | | | }} | |||
{{Family tree| I04 | | I05 | | I06 | | |!| | | |!| | | |!| | | |!| | | |!| | | | | | | | | | |I04=Major idiopathic interstitial pneumonias|I05=Rare idiopathic interstitial pneumonias|I06=Unclassifiable idiopathic interstitial pneumonias}} | |||
{{Family tree| |!| | | |!| | | | | | | |!| | | |!| | | |!| | | |!| | | |!| | | | | | | | | |}} | |||
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{{Family tree|boxstyle=text-align: left; | J01 | | J02 | | | | | | J07 | | J09 | | J08 | | J10 | | J11 | | | | | | | | |J01=• Idiopathic pulmonary fibrosis<br>• Idiopathic nonspecific interstitial pneumonia<br>• Respiratory bronchiolitis-interstitial lung disease<br>• Desquamative interstitial pneumonia<br>• Cryptogenic organising pneumonia<br>• Acute interstitial pneumonia<br>|J02=• Idiopathic lymphoid interstitial pneumonia<br>• Idiopathic pleuroparenchymal fibroelastosis<br>|J07=• Systemic lupus erythematosus<br>• Rheumatoid arthritis<br>• Ankylosing spondylitis<br>• Systemic sclerosis<br>• Sjögren syndrome<br>• Polymyositis<br>• Dermatomyositis<br>|J08=• Tuberous sclerosis<br>• Neurofibromatosis<br>• Niemann-Pick disease<br>• Gaucher disease<br>• Hermansky-Pudlak syndrome<br>|J09=• Crohn disease<br>• Primary biliary cirrhosis<br>• Chronic active hepatitis<br>• Ulcerative colitis<br>|J10=• Bone marrow transplantation<br>• Solid organ transplantation<br>|J11=• Goodpasture syndrome<br>• Idiopathic pulmonary hemosiderosis<br>• Isolated pulmonary capillaritis | |||
|}} | |||
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==Pathophysiology== | ==Pathophysiology== |
Revision as of 21:43, 7 March 2018
For the WikiPatient page for this topic, click here
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Saarah T. Alkhairy, M.D.
Synonyms and keywords: Diffuse parenchymal lung disease; DPLD; ILD
Overview
Classification
Interstitial lung disease | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Lung Response: Granulomatous | Lung Response: Alveolitis, Interstitial Inflammation, and Fibrosis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Known | Idiopathic (Unknown) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Hypersensitivity pneumonitis (organic dusts) | Inorganic dusts | Sarcoidosis | Lymphomatoid granulomatosis | Granulomatous vasculitides | Bronchocentric granulomatosis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Beryllium | Silica | Eosinophilic granulomatosis with polyangiitis (Churg Strauss syndrome) | Granulomatosis with polyangiitis (Wegener) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Known cause | Idiopathic (Unknown) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Drug-induced pulmonary toxicity | Occupational and environmental exposure | Radiation-induced lung injury | Aspiration pneumonia | Smoking-related | Residual of acute respiratory distress syndrome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Inhaled inorganic dust | Inhaled organic dusts | Inhaled agents other than inorganic or organic dusts | Desquamative interstitial pneumonia | Respiratory bronchiolitis–associated interstitial lung disease | Pulmonary Langerhans cell granulomatosis | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Pulmonary alveolar proteinosis | Idiopathic interstitial pneumonias | Lymphocytic infiltrative disorders (lymphocytic interstitial pneumonitis associated with connective tissue disease) | Connective tissue diseases | Gastrointestinal or liver diseases | Inherited diseases | Graft-versus-host disease | Pulmonary hemorrhage syndromes | Eosinophilic pneumonias | Lymphangioleiomyomatosis | Amyloidosis | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Major idiopathic interstitial pneumonias | Rare idiopathic interstitial pneumonias | Unclassifiable idiopathic interstitial pneumonias | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
• Idiopathic pulmonary fibrosis • Idiopathic nonspecific interstitial pneumonia • Respiratory bronchiolitis-interstitial lung disease • Desquamative interstitial pneumonia • Cryptogenic organising pneumonia • Acute interstitial pneumonia | • Idiopathic lymphoid interstitial pneumonia • Idiopathic pleuroparenchymal fibroelastosis | • Systemic lupus erythematosus • Rheumatoid arthritis • Ankylosing spondylitis • Systemic sclerosis • Sjögren syndrome • Polymyositis • Dermatomyositis | • Crohn disease • Primary biliary cirrhosis • Chronic active hepatitis • Ulcerative colitis | • Tuberous sclerosis • Neurofibromatosis • Niemann-Pick disease • Gaucher disease • Hermansky-Pudlak syndrome | • Bone marrow transplantation • Solid organ transplantation | • Goodpasture syndrome • Idiopathic pulmonary hemosiderosis • Isolated pulmonary capillaritis | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Pathophysiology
References
Template:Respiratory pathology
de:Interstitielle Lungenerkrankung
fi:Keuhkoparenkyymisairaudet