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Acute Interstitial Pneumonia (Hamman Rich Syndrome)

Abstract
Acute interstitial pneumonia (AIP - also known as Hamman-Rich syndrome) is an acute, rapidly progressive idiopathic pulmonary disease that often leads to fulminant respiratory failure and acute respiratory distress syndrome (ARDS).[1] It can be distinguished clinically from other types of interstitial pneumonia by the rapid onset of respiratory failure in a patient without preexisting lung disease.[2] Louis Hamman and Arnold Rich first described it in 1935 as a fulminating diffuse interstitial fibrosis of the lungs.[3] In 1986, Katzenstein introduced the term AIP differentiating it from the group of chronic interstitial pneumonia.[4][5] The American Thoracic Society (ATS) and European Respiratory Society (ERS) classify AIP under major idiopathic interstitial pneumonia, compared to other rare or unclassified idiopathic interstitial pneumonia.[1]

Publisher

StatPearls Publishing
Treasure Island (FL)

Language

eng

PubMed ID

32119316

Citation

Mrad A, Huda N: Acute Interstitial Pneumonia (Hamman Rich Syndrome). StatPearls. StatPearls Publishing, 2020, Treasure Island (FL).
Mrad A, Huda N. Acute Interstitial Pneumonia (Hamman Rich Syndrome). StatPearls. StatPearls Publishing; 2020.
Mrad A & Huda N. (2020). Acute Interstitial Pneumonia (Hamman Rich Syndrome). In StatPearls. Treasure Island (FL): StatPearls Publishing
Mrad A, Huda N. Acute Interstitial Pneumonia (Hamman Rich Syndrome). StatPearls. Treasure Island (FL): StatPearls Publishing; 2020.
* Article titles in AMA citation format should be in sentence-case
TY - CHAP T1 - Acute Interstitial Pneumonia (Hamman Rich Syndrome) BT - StatPearls A1 - Mrad,Ali, AU - Huda,Najia, Y1 - 2020/01// PY - 2020/3/3/pubmed PY - 2020/3/3/medline PY - 2020/3/3/entrez N2 - Acute interstitial pneumonia (AIP - also known as Hamman-Rich syndrome) is an acute, rapidly progressive idiopathic pulmonary disease that often leads to fulminant respiratory failure and acute respiratory distress syndrome (ARDS).[1] It can be distinguished clinically from other types of interstitial pneumonia by the rapid onset of respiratory failure in a patient without preexisting lung disease.[2] Louis Hamman and Arnold Rich first described it in 1935 as a fulminating diffuse interstitial fibrosis of the lungs.[3] In 1986, Katzenstein introduced the term AIP differentiating it from the group of chronic interstitial pneumonia.[4][5] The American Thoracic Society (ATS) and European Respiratory Society (ERS) classify AIP under major idiopathic interstitial pneumonia, compared to other rare or unclassified idiopathic interstitial pneumonia.[1] PB - StatPearls Publishing CY - Treasure Island (FL) UR - https://www.unboundmedicine.com/medline/citation/32119316/StatPearls:_Acute_Interstitial_Pneumonia_(Hamman_Rich_Syndrome) L2 - https://www.ncbi.nlm.nih.gov/books/NBK554429 DB - PRIME DP - Unbound Medicine ER -
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