Related Experiment Video
Updated: Jun 10, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Systemic JIA-Associated Lung Disease: A Multicenter Analysis of Clinical Features, Treatment Challenges, and Outcomes
Dilara Unal1, Veysel Cam1, Elif Kilic Konte2
1Department of Pediatric Rheumatology, Hacettepe University, Ankara, Turkey.
Background:
Systemic juvenile idiopathic arthritis (sJIA) (Still's disease) associated lung disease (sJIA-LD) is a rare but severe complication, characterized by pulmonary involvement with high morbidity and mortality rates. While the incidence of sJIA-LD has increased, its pathogenesis and risk factors remain poorly understood.
Objectives:
This multicenter retrospective study aimed to evaluate the clinical, radiological, and laboratory features of patients with sJIA-LD, assess the impact of prior biologic treatments, and analyze treatment outcomes.
Methods:
Data were collected from 18 patients diagnosed with sJIA-LD between 2007 and 2024 across five pediatric rheumatology clinics in our country. Clinical features, imaging findings, and treatment regimens before and after sJIA-LD diagnosis were analyzed. HLA-DRB1*15 typing was performed in a subset of patients.
Results:
The median age of sJIA-LD diagnosis was 11.21 years, with a median disease duration of 2.76 years from sJIA diagnosis. Macrophage activation syndrome (MAS) occurred in 88.9% of patients prior to the diagnosis of lung disease. Cough (100%), dyspnea (83.3%), and clubbing (50%) were the most common clinical manifestations. Ground-glass opacities were the most frequent imaging finding (61.1%). DRESS was observed in 11.1% of patients, with 27.7% experiencing adverse reactions to biologics. Treatment revision after sJIA-LD diagnosis occurred in 83.3% of patients, with JAK inhibitors demonstrating clinical improvement in some cases. The overall survival rate was 94.4%, with one death due to fulminant MAS.
Conclusion:
This study provides data from a geographically underreported population in Turkey and the Eastern Mediterranean region. In our cohort, treatment modification after sJIA-LD diagnosis was common, while biologic therapy was often continued. These findings highlight the heterogeneous course of sJIA-LD. Further prospective multicenter studies are needed to optimize treatment strategies and improve risk stratification.
Related Concept Videos
Chronic Obstructive Pulmonary Disease-IV: Assessement and Diagnostic Studies
Medical History
COPD: Pathogenesis and Clinical Features
The primary cause for the onset of COPD is cigarette smoking and exposure to air pollution. These hazardous factors initiate a chain reaction within the lungs, resulting in chronic inflammation, damage to the airways, and a...
Chronic Obstructive Pulmonary Disease IV: Clinical Manifestations
Chronic Obstructive Pulmonary Disease-V: Management
Smoking Cessation
Chronic Obstructive Pulmonary Disease III: Chronic Bronchitis Features
Chronic Obstructive Pulmonary Disease-III: Symptoms and Complications.
Symptoms of COPD can be classified as primary or systemic. Primary symptoms relate to reduced airflow, while systemic or extrapulmonary symptoms relate to COPD's broader impact on the body.
Primary Symptoms of COPD:
