Systemic sclerosis-associated interstitial lung disease
A Perelas, RM Silver, AV Arrossi… - The Lancet respiratory …, 2020 - thelancet.com
Systemic sclerosis is an autoimmune connective tissue disease, which is characterised by
immune dysregulation and progressive fibrosis that typically affects the skin, with variable …
immune dysregulation and progressive fibrosis that typically affects the skin, with variable …
Mechanisms of progressive fibrosis in connective tissue disease (CTD)-associated interstitial lung diseases (ILDs)
P Spagnolo, O Distler, CJ Ryerson… - Annals of the …, 2021 - ard.bmj.com
Interstitial lung diseases (ILDs), which can arise from a broad spectrum of distinct
aetiologies, can manifest as a pulmonary complication of an underlying autoimmune and …
aetiologies, can manifest as a pulmonary complication of an underlying autoimmune and …
Update of EULAR recommendations for the treatment of systemic sclerosis
O Kowal-Bielecka, J Fransen, J Avouac… - Annals of the rheumatic …, 2017 - Elsevier
The aim was to update the 2009 European League against Rheumatism (EULAR)
recommendations for the treatment of systemic sclerosis (SSc), with attention to new …
recommendations for the treatment of systemic sclerosis (SSc), with attention to new …
Myeloablative autologous stem-cell transplantation for severe scleroderma
KM Sullivan, EA Goldmuntz… - … England Journal of …, 2018 - Mass Medical Soc
Background Despite current therapies, diffuse cutaneous systemic sclerosis (scleroderma)
often has a devastating outcome. We compared myeloablative CD34+ selected autologous …
often has a devastating outcome. We compared myeloablative CD34+ selected autologous …
Mycophenolate mofetil versus oral cyclophosphamide in scleroderma-related interstitial lung disease (SLS II): a randomised controlled, double-blind, parallel group …
DP Tashkin, MD Roth, PJ Clements… - The lancet Respiratory …, 2016 - thelancet.com
Background 12 months of oral cyclophosphamide has been shown to alter the progression
of scleroderma-related interstitial lung disease when compared with placebo. However …
of scleroderma-related interstitial lung disease when compared with placebo. However …
Interstitial lung disease associated with systemic sclerosis (SSc-ILD)
V Cottin, KK Brown - Respiratory research, 2019 - Springer
Abstract Background Systemic sclerosis (SSc) is a rare connective tissue disease with a
heterogeneous clinical course. Interstitial lung disease (ILD) is a common manifestation of …
heterogeneous clinical course. Interstitial lung disease (ILD) is a common manifestation of …
Treatment of systemic sclerosis–associated interstitial lung disease: evidence-based recommendations. An official American Thoracic Society clinical practice …
G Raghu, SB Montesi, RM Silver, T Hossain… - American journal of …, 2024 - atsjournals.org
Background: Interstitial lung disease (ILD) is a significant cause of morbidity and mortality in
patients with systemic sclerosis (SSc). To date, clinical practice guidelines regarding …
patients with systemic sclerosis (SSc). To date, clinical practice guidelines regarding …
Management of interstitial lung disease associated with connective tissue disease
The lung is a common site of complications of systemic connective tissue disease (CTD),
and lung involvement can present in several ways. Interstitial lung disease (ILD) and …
and lung involvement can present in several ways. Interstitial lung disease (ILD) and …
Systemic sclerosis
Y Allanore, R Simms, O Distler… - Nature reviews Disease …, 2015 - nature.com
Systemic sclerosis is a complex autoimmune disease characterized by a chronic and
frequently progressive course and by extensive patient-to-patient variability. Like other …
frequently progressive course and by extensive patient-to-patient variability. Like other …
Systemic sclerosis
CP Denton, D Khanna - The Lancet, 2017 - thelancet.com
Systemic sclerosis, also called scleroderma, is an immune-mediated rheumatic disease that
is characterised by fibrosis of the skin and internal organs and vasculopathy. Although …
is characterised by fibrosis of the skin and internal organs and vasculopathy. Although …