Integrating Clinics, Laboratory, and Imaging for the Diagnosis of Common Variable Immunodeficiency-Related Granulomatous-Lymphocytic Interstitial Lung Disease.

Fecha de publicación: Fecha Ahead of Print:

Autores de IIS La Fe

Participantes ajenos a IIS La Fe

  • Forner Giner, Maria Jose

Grupos

Abstract

Granulomatous-lymphocytic interstitial lung disease (GLILD) is a distinct clinic-radio-pathological interstitial lung disease (ILD) that develops in 9% to 30% of patients with common variable immunodeficiency (CVID). Often related to extrapulmonary dysimmune disorders, it is associated with long-term lung damage and poorer clinical outcomes. The aim of this study was to explore the potential use of the integration between clinical parameters, laboratory variables, and developed CT scan scoring systems to improve the diagnostic accuracy of non-invasive tools.

Copyright © 2022 Cabanero-Navalon, Garcia-Bustos, Forero-Naranjo, Baettig-Arriagada, Núñez-Beltrán, Cañada-Martínez, Forner Giner, Catalán-Cáceres, Martínez Francés and Moral Moral.

Datos de la publicación

ISSN/ISSNe:
1664-3224, 1664-3224

Frontiers in Immunology  FRONTIERS MEDIA SA

Tipo:
Article
Páginas:
813491-813491
PubMed:
35281075
Factor de Impacto:
2,331 SCImago
Cuartil:
Q1 SCImago

Citas Recibidas en Web of Science: 17

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Keywords

  • CVID, GLILD, common variable immunodeficiency, diagnosis, interstitial lung disease, predictive model, scoring system, splenomegaly

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