Clinical manifestations and diagnostic challenges in interstitial pneumonia with autoimmune features. Case report

Introduction: Interstitial pneumonia with autoimmunex characteristics (IPAF) is a very little-known entity that groups individuals with diffuse interstitial lung disease who have clinical, serological, or morphological characteristics that suggest a connective tissue disease, but without meeting rhe...

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Detaylı Bibliyografya
Yazar:	Santo-Cepeda, Kristopher (author)
Diğer Yazarlar:	Vergara-Centeno, José (author), Astudillo-Córdova , Madeline (author), Guzñay-Pinto , Camilo (author)
Materyal Türü:	article
Dil:	spa
Baskı/Yayın Bilgisi:	2025
Konular:	neumonía intersticial autoinmunidad anticuerpos fibrosis pulmonar idiopatica informe de casos interstitial pneumonia autoimmunity antibodies idiopatic pulmonary fibrosis case reports
Online Erişim:	https://revistadigital.uce.edu.ec/index.php/CIENCIAS_MEDICAS/article/view/6770
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Clinical manifestations and diagnostic challenges in interstitial pneumonia with autoimmune features. Case report

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