|
Accession number;02A0539963
|
| Title;Clinical Exmination. Intertitial pneumonia. |
| Author;
KONDO YASUHIRO
(Koritsutoseibyoin Kokyuki・areruginaika Dainibu)
TANIGUCHI HIROYUKI
(Koritsutoseibyoin Kokyuki・areruginaika Daiichibu)
|
Journal Title;Clinic All-round
|
Journal Code:Z0697A
|
ISSN:0371-1900
|
|
VOL.51;NO.;PAGE.1259-1263(2002)
|
| Figure&Table&Reference;TBL.1, REF.10 |
| Pub. Country;Japan |
| Language;Japanese |
| Abstract;The idiopathic pulmonary fibrosis (IPF) is made to be a disease insufficient for the prevention of chronic advancing with many frequencies in the interstitial pneumonia of unknown origin.The international mutual agreement declaration on idiopathic pulmonary fibrosis and interstitial pneumonia of unknown origin was announced in 2000 by American thoracic disease institute and European pneumology association. The examination planning method considering the differentiation with various diffusive lung diseases was outlined on interstitial pneumonia of the unknown origin (IIPs), especially, focusing on the IPF among them. Important information is given by the high resolution CT (HRCT) in the diagnosis of the interstitial pneumonia. The general HRCT image of IPF is the reticular change of both lungs bottom of the peripheral division pleura. The differentiation between IIPs and other diffusive lung disease was also mentioned. |
|
|
|
Related Articles;
|
