Pulmonary involvement in systemic sclerosis

Systemic sclerosis (SSc) is a multi-systemic autoimmune disease that mainly affects the skin, lungs, gastrointestinal tract, heart and kidneys. Pulmonary disease in patients with SSc is strongly associated with mortality. The mechanisms involved into its pathophysiology include the activation of aut...

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Autores:
Tipo de recurso:
Fecha de publicación:
2016
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/23245
Acceso en línea:
https://doi.org/10.1016/j.autrev.2016.07.025
https://repository.urosario.edu.co/handle/10336/23245
Palabra clave:
Biological marker
Aspiration bronchiolitis
Aspiration pneumonia
Bronchiolitis
Bronchiolocentric fibrosis
Clinical feature
Combined pulmonary fibrosis and emphysema
Diaphragm disease
Diffuse alveolar damage
Epidemiology
Histopathology
Human
Interstitial pneumonia
Lung cancer
Lung disease
Lung emphysema
Lung fibrosis
Lung hemorrhage
Lung infection
Non specific interstitial pneumonia
Organizing pneumonia
Pathophysiology
Pulmonary capillary hemangiomatosis
Pulmonary hypertension
Pulmonary veno-occlusive disease
Review
Systematic review
Systemic sclerosis
Thorax radiography
Usual interstitial pneumonia
Complication
Diagnostic imaging
Female
Immunology
Lung
Male
Pathology
Systemic sclerosis
X-ray computed tomography
Female
Humans
Lung
Male
Pathology
Pulmonary involvement
Radiology
Systemic sclerosis
Tomography
X-ray computed
interstitial
x-ray computed
interstitial
systemic
Lung diseases
Lung diseases
Scleroderma
Tomography
Rights
License
Abierto (Texto Completo)
Description
Summary:Systemic sclerosis (SSc) is a multi-systemic autoimmune disease that mainly affects the skin, lungs, gastrointestinal tract, heart and kidneys. Pulmonary disease in patients with SSc is strongly associated with mortality. The mechanisms involved into its pathophysiology include the activation of autoimmune cells and hyperplasia of fibroblasts with an increased capacity to produce collagen and diminished collagen breakdown. Although pulmonary biopsy is the gold standard for the diagnosis of interstitial lung disease in SSc, the most commonly used method is high-resolution computed tomography due to its high sensitivity and specificity. Herein, a comprehensive review on the pulmonary involvement in SSc is presented highlighting the radiologic–pathologic correlations. © 2016 Elsevier B.V.