Idiopathic interstitial pneumonia

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Idiopathic interstitial pneumonia
Classification and external resources
Usual interstitial pneumonia (1).JPG
Micrograph of usual interstitial pneumonia (UIP). UIP is the most common pattern of idiopathic interstitial pneumonia and usually represents idiopathic pulmonary fibrosis. H&E stain. Autopsy specimen.

Idiopathic interstitial pneumonia (IIP), or noninfectious pneumonia[1] are a class of diffuse lung diseases. It is a term used for a type of diffuse parenchymal lung disease (DPLD), also called interstitial lung disease (ILD).
There are seven distinct subtypes of IIP.

Histologic classification[edit]

Classification can be complex,[2] and the combined efforts of clinicians, radiologists, and pathologists can help in the generation of a more specific diagnosis.[3][4]

Idiopathic interstitial pneumonia can be subclassified based on histologic appearance into the following patterns:[5][6]

Histology Clinical Correlates
Desquamative interstitial pneumonia (DIP) DIP
Diffuse alveolar damage (DAD) ARDS, AIP, TRALI
Nonspecific interstitial pneumonia (NSIP) NSIP
Respiratory bronchiolitis RB-ILD
Usual interstitial pneumonia (UIP) CVD, IPF, drug toxicity, pneumoconiosis
Organizing pneumonia Cryptogenic organizing pneumonia
Lymphoid interstitial pneumonia (LIP) LIP

Usual interstitial pneumonia is the most common type.[7]

Development[edit]

Table 1: Development of the (histologic) idiopathic interstitial pneumonia classification

 
 
 
Leibow et al. (1969)
 
Katzenstein (1998)[8]
 
ATS/ERS (2002)[6]
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
UIP
 
UIP
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
UIP
 
 
DAD
 
DAD
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
NSIP
 
NSIP
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
DIP
 
DIP/RB
 
DIP
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
RB
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
BIP
 
OP
 
OP
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
LIP
 
(LPD)
 
LIP
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
GIP
 
(HMF)
 
(HMF)
 
 

UIP=usual interstitial pneumonia; DAD=diffuse alveolar damage; NSIP=non-specific interstitial pneumonia; DIP=desquamative interstitial pneumonia; RB=respiratory bronchiolitis; BIP=bronchiolitis obliterans interstitial pneumonia; OP=organizing pneumonia; LIP=lymphoid interstitial pneumonia; LPD=lymphoproliferative disease (not considered a diffuse lung disease); GIP=giant cell interstitial pneumonia; HMF=heavy metal fibrosis, no longer grouped with diffuse lung disease

Lymphoid interstitial pneumonia was originally included in this category, then excluded, then included again.[9]

References[edit]

  1. ^ Clinical infectious diseases : a practical approach. New York, NY [u.a.]: Oxford Univ. Press. 1999. p. 833. ISBN 978-0-19-508103-9. 
  2. ^ Nicholson AG (November 2002). "Classification of idiopathic interstitial pneumonias: making sense of the alphabet soup". Histopathology 41 (5): 381–91. doi:10.1046/j.1365-2559.2002.01421.x. PMID 12405906. 
  3. ^ Flaherty KR, King TE, Raghu G, et al. (October 2004). "Idiopathic interstitial pneumonia: what is the effect of a multidisciplinary approach to diagnosis?". Am. J. Respir. Crit. Care Med. 170 (8): 904–10. doi:10.1164/rccm.200402-147OC. PMID 15256390. 
  4. ^ Kim DS, Collard HR, King TE (June 2006). "Classification and natural history of the idiopathic interstitial pneumonias". Proc Am Thorac Soc 3 (4): 285–92. doi:10.1513/pats.200601-005TK. PMC 2658683. PMID 16738191. 
  5. ^ Leslie KO, Wick MR. Practical Pulmonary Pathology: A Diagnostic Approach. Elsevier Inc. 2005. ISBN 978-0-443-06631-3.
  6. ^ a b American Thoracic, Society; European Respiratory, Society (January 2002). "American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias. This joint statement of the American Thoracic Society (ATS), and the European Respiratory Society (ERS) was adopted by the ATS board of directors, June 2001 and by the ERS Executive Committee, June 2001". Am. J. Respir. Crit. Care Med. 165 (2): 277–304. PMID 11790668. 
  7. ^ Visscher DW, Myers JL (June 2006). "Histologic spectrum of idiopathic interstitial pneumonias". Proc Am Thorac Soc 3 (4): 322–9. doi:10.1513/pats.200602-019TK. PMID 16738196. 
  8. ^ Katzenstein AL, Myers JL (1998). "Idiopathic pulmonary fibrosis: clinical relevance of pathologic classification". Am. J. Respir. Crit. Care Med. 157 (4 Pt 1): 1301–15. PMID 9563754. 
  9. ^ Swigris JJ, Berry GJ, Raffin TA, Kuschner WG (December 2002). "Lymphoid interstitial pneumonia: a narrative review". Chest 122 (6): 2150–64. doi:10.1378/chest.122.6.2150. PMID 12475860.