Document Detail

Clinically occult subpleural fibrosis and acute interstitial pneumonia a precursor to idiopathic pulmonary fibrosis?
MedLine Citation:
PMID:  18399864     Owner:  NLM     Status:  MEDLINE    
BACKGROUND AND OBJECTIVE: The clinical features and acute component of the pathological findings in patients with acute exacerbation of IPF are similar to those of acute interstitial pneumonia (AIP). A growing body of research suggests that acute exacerbation of subclinical IPF is similar to AIP. This study tested the hypothesis that subpleural fibrosis (resembling localized usual interstitial pneumonia) in patients with diffuse alveolar damage can mimic patients with AIP alone. METHODS: The clinical, radiological and histopathological characteristics of patients with AIP with or without subpleural fibrosis, as identified at post-mortem examination, were assessed. RESULTS: Fourteen patients with AIP met the inclusion criteria. These comprised nine men and five women ranging in age from 65 to 90 years. The mean duration from onset of symptoms to admission was 12.3 days, and from admission to death was 50.5 days. All patients presented with severe respiratory failure with bilateral pulmonary infiltrates on CXR. CT scans revealed bilateral ground glass opacity (100.0%), air space consolidation (69.2%) and no honeycombing. In seven patients (50.0%) histological examination showed subpleural fibrosis. There were no differences in the clinicopathological or CT scan findings between patients with AIP only compared with those with AIP and subpleural fibrosis. CONCLUSIONS: Subpleural fibrosis resembling localized usual interstitial pneumonia is often present in patients diagnosed as having AIP. These patients were not distinguishable from those with AIP only, based on the clinicopathological and radiological findings.
Jun Araya; Yoshinori Kawabata; Park Jinho; Takashi Uchiyama; Hideo Ogata; Yutaka Sugita
Related Documents :
19657984 - Choroidal folds in acute vogt-koyanagi-harada disease.
8287644 - Tumour necrosis factor-alpha, resting energy expenditure and cachexia in cystic fibrosis.
16202784 - The survival advantage of patients with cystic fibrosis diagnosed through neonatal scre...
9292244 - Pathogenesis and management of delayed orthostatic hypotension in patients with chronic...
23274554 - Cystic "feminine" pancreatic neoplasms in men. do any clinical alterations correlate wi...
21967574 - Achalasia secondary to neoplasia: a disease with a changing differential diagnosis.
Publication Detail:
Type:  Comparative Study; Journal Article    
Journal Detail:
Title:  Respirology (Carlton, Vic.)     Volume:  13     ISSN:  1440-1843     ISO Abbreviation:  Respirology     Publication Date:  2008 May 
Date Detail:
Created Date:  2008-04-10     Completed Date:  2008-07-29     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9616368     Medline TA:  Respirology     Country:  Australia    
Other Details:
Languages:  eng     Pagination:  408-12     Citation Subset:  IM    
Section of Pathology, Saitama Cardiovascular and Respiratory Center, Saitama, Japan.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Acute Disease
Aged, 80 and over
Diagnosis, Differential
Lung Diseases, Interstitial / diagnosis,  pathology*,  radiography*
Pleura / pathology,  radiography
Pulmonary Alveoli / pathology,  radiography
Pulmonary Fibrosis / diagnosis,  pathology*,  radiography*
Retrospective Studies
Tomography, X-Ray Computed

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Predictors for failed dose reduction of inhaled corticosteroids in childhood asthma.
Next Document:  Solid-organ malignancy as a risk factor for tuberculosis.