Autopsy findings in a case of idiopathic pleuroparenchymal fibroelastosis: A rare entity with review of literature

نویسندگان

چکیده

Idiopathic pleuroparenchymal fibroelastosis is a rare idiopathic interstitial pneumonia which mainly affects the upper lobe of lungs resulting in intra alveolar fibrosis, elastosis and visceral pleural fibrosis. For definite diagnosis, radiographic findings as well histopathology are required. The overlap with lung diseases seen usually, makes it challenging to diagnose. There no guidelines available for diagnosis appropriate management this disease only few cases reported literature. We report case autopsy 32-year-old female who allegedly died heart failure review

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WITHDRAWN: Idiopathic pleuroparenchymal fibroelastosis: A rare but increasingly recognized entity.

This article has been withdrawn for editorial reasons because the journal will be published only in English. In order to avoid duplicated records, this article can be found at http://dx.doi.org/10.1016/j.rppnen.2014.04.008. The Publisher apologizes for any inconvenience this may cause. The full Elsevier Policy on Article Withdrawal can be found at http://www.elsevier.com/locate/withdrawalpolicy.

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Idiopathic pleuroparenchymal fibroelastosis – A rare idiopathic interstitial pneumonia

Idiopathic pleuroparenchymal fibroelastosis is a rare idiopathic interstitial pneumonia. It was first described in 2004 and subsequently included in the ATS/ERS classification of idiopathic interstitial pneumonia in 2013. There have been few cases reported so far. The diagnostic criteria is still emerging and its etiology is being questioned. We report a case of pleuroparenchymal fibroelastosis...

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ژورنال

عنوان ژورنال: Indian Journal of Pathology and Oncology

سال: 2023

ISSN: ['2394-6784', '2394-6792']

DOI: https://doi.org/10.18231/j.ijpo.2023.037