1988
DOI: 10.1016/0007-0971(88)90042-3
|View full text |Cite
|
Sign up to set email alerts
|

Cryptogenic bilateral fibrosing pleuritis

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

1
24
0

Year Published

1990
1990
2013
2013

Publication Types

Select...
4
4
1

Relationship

1
8

Authors

Journals

citations
Cited by 42 publications
(25 citation statements)
references
References 31 publications
1
24
0
Order By: Relevance
“…Familial cryptogenic fibrosing pleuritis that is unresponsive to corticosteroids has been described in association with Fanconi’s syndrome [9]. Buchanan et al [10]describe four cases of cryptogenic bilateral fibrosing pleuritis with similar features to our cases. Focal collections of lymphocytes were present in the cases described.…”
Section: Discussionmentioning
confidence: 65%
“…Familial cryptogenic fibrosing pleuritis that is unresponsive to corticosteroids has been described in association with Fanconi’s syndrome [9]. Buchanan et al [10]describe four cases of cryptogenic bilateral fibrosing pleuritis with similar features to our cases. Focal collections of lymphocytes were present in the cases described.…”
Section: Discussionmentioning
confidence: 65%
“…It is characterized radiologically by features suggestive of a chronic interstitial pneumonia with upper lobe predominance, and histologically by pleural fibrosis and parenchymal fibroelastosis in a predominantly subpleural distribution, with a sharp demarcation between fibroelastotic and unaffected lung parenchyma, and with the presence of fibroblastic foci at this interface. A limited number of cases with similar radiologic and pathologic features have also been reported, [8][9][10][11][12][13][14] including a very recent article by Reddy et al, 14 suggesting a broader spectrum of histopathologic findings.…”
Section: Discussionmentioning
confidence: 99%
“…Several cases and small series with similar radiologic and pathologic features have also been reported. [8][9][10][11][12][13][14] Radiologically, idiopathic pleuroparenchymal fibroelastosis has been characterized by pleural thickening associated with underlying parenchymal reticular abnormalities, architectural distortion and traction bronchiectasis in a mostly upper lobepredominant distribution. 7,10,11 Histologically, idiopathic pleuroparenchymal fibroelastosis is characterized by pronounced visceral pleural fibrosis associated with subpleural, 'intra-alveolar' fibrotic changes characterized by an admixture of elastic and fibrous tissue (fibroelastosis).…”
mentioning
confidence: 99%
“…Pleural fibrosis is most commonly caused by asbestos exposure and may follow asbestos-related benign pleural effusion,1 tuberculous pleural effusion, haemothorax, use of ergot derivatives, and occasionally rheumatoid pleurisy, uremic pleuritis or coronary artery bypass graft surgery; rarely it may remain idiopathic,1 , 2 occasionally in a familial context 3 , 4. Mediastinal fibrosis may develop as a consequence of histoplasmosis or tuberculosis, or rarely actinomycosis, syphilis, aspergillosis, sarcoidosis, silicosis or methysergide exposure, or it may remain idiopathic 5.…”
Section: Discussionmentioning
confidence: 99%