Zobrazeno 1 - 10
of 19
pro vyhledávání: '"11"'
Autor:
I. González-Mazón, Lara Sánchez Bilbao, Diana Prieto-Peña, José Luis Martín-Varillas, Miguel A. González-Gay, Monica Calderón-Goercke, Ricardo Blanco, R. Demetrio-Pablo, Vanesa Calvo-Río, Raúl Fernández Ramón, Belén Atienza-Mateo
Publikováno v:
Poster Presentations.
Background: Sarcoidosis is a multisystemic inflammatory disease characterized by non-caseating epitheliod granulomas that can affect any organ system. The three most frequency affected organs are lung, skin and eyes. Ocular involvement is the present
Autor:
Francesco Masini, Emanuele Pinotti, Teresa Salvatore, Monaco Lucio, Roberta Ferrara, Klodian Gjeloshi, Giovanna Cuomo
Publikováno v:
Abstracts Accepted for Publication.
Background Systemic Sclerosis (SSc) is a multisystem connective disease characterized by a microvascular damage, which leads to systemic fibrosis, immune dysregulation and progressive involvement of internal organs [1]. According to the classificatio
Publikováno v:
THURSDAY, 14 JUNE 2018.
Background Lung diseases, such as airway disease and interstitial lung disease (ILD), are often complicated in patients with rheumatoid arthritis (RA). The presence of those pre-existing lung diseases is one of the poor prognostic factors and risk fa
Autor:
M. Di Carlo, Fausto Salaffi, Andrea Giovagnoni, Armando Gabrielli, Marina Carotti, Paolo Fraticelli
Publikováno v:
THURSDAY, 14 JUNE 2018.
Background Esophageal dilation and dysfunction has been implicated in the pathogenesis of interstitial lung disease (ILD) in systemic sclerosis (SSc). Objectives The aims of this were to explore the association of the esophageal dilation and ILD on c
Publikováno v:
Poster Presentations.
Background Pulmonary fibrosis is one of the gravest manifestations of Systemic Sclerosis (SSc) and conventional DMARDs therapy has not shown any particular positive effect. Objectives Our goal was to see whether the elimination pf B - lymphocytes thr
Publikováno v:
Diagnostics and imaging procedures.
Background Granulomatosis with polyangiitis(GPA) mainly involves the upper and lower respiratory tracts and kidneys and induces necrotising vasculitis and granuloma. Nasal biopsy has been recommended in GPA-suspected patients to not only completely c
Autor:
Philippe Dieudé, Marine Forien, Bruno Crestani, Raphael Borie, Khadija Benali, Lucie Demaria, Sébastien Ottaviani
Publikováno v:
Abstracts Accepted for Publication.
Background Bone sarcoidosis: usefulness of 18F-FDG PET/CT Objectives Bone sarcoidosis is usually rare but more sensitive imaging procedures such as 18F-fluorodeoxyglucose Positron Emission Tomography/Computed Tomography (18F-FDG PET/CT) allow a bette
Publikováno v:
Abstracts Accepted for Publication.
Background Lung involvement has been reported in 10-20% of patients (pts) with primary Sjogren’s syndrome (pSS) and mostly affecting parenchyma and airways. Its occurrence significantly impacts both quality of life and mortality in pSS pts. Objecti
Autor:
Felipe Reyes, Caterina Chesta, Karen Vergara, Annelise Goecke, Sebastián M. Chávez, Silvana Saavedra
Publikováno v:
Abstracts Accepted for Publication.
Background Diffuse parenchymal pulmonary diseases, called interstitial lung diseases, are a heterogeneous group of disorders that are classified together due to clinical, radiographic, physiological or similar pathological manifestations1.The diagnos
Autor:
Santos Castaeda, Juan M. Serrador, Bianca Barreira, Carlos Gamallo, Mara De la Fuente-Fernndez, Antonio Muoz-Callejas, Daniel Morales-Cano, Ana Urzainqui, Francisco Prez-Vizcano, Javier Silvn, Rafael Gonzlez-Tajuelo, Esther Vicente, Angel Cogolludo
Publikováno v:
Poster Presentations.
Background Pulmonary arterial hypertension (PAH) is a rare disease with unknown etiopathogenesis and no curative treatment [1]. PAH is one of the major complications of connective tissue diseases, and 7-15% of patients with systemic sclerosis (SSc) d