Pulmonary Hypertension and Other Potentially Fatal Pulmonary Complications in Systemic Juvenile Idiopathic Arthritis

@article{Kimura2013PulmonaryHA,
  title={Pulmonary Hypertension and Other Potentially Fatal Pulmonary Complications in Systemic Juvenile Idiopathic Arthritis},
  author={Y. Kimura and J. E. Weiss and Kathryn L Haroldson and Tzielan C. Lee and M. Punaro and S. Oliveira and E. Rabinovich and M. Riebschleger and J. Ant{\'o}n and P. Blier and V. Gerloni and M. Hazen and Elizabeth Kessler and K. Onel and M. Passo and R. Rennebohm and C. Wallace and P. Woo and N. Wulffraat},
  journal={Arthritis Care & Research},
  year={2013},
  volume={65}
}
  • Y. Kimura, J. E. Weiss, +16 authors N. Wulffraat
  • Published 2013
  • Medicine
  • Arthritis Care & Research
  • Systemic juvenile idiopathic arthritis (JIA) is characterized by fevers, rash, and arthritis, for which interleukin‐1 (IL‐1) and IL‐6 inhibitors appear to be effective treatments. Pulmonary arterial hypertension (PAH), interstitial lung disease (ILD), and alveolar proteinosis (AP) have recently been reported with increased frequency in systemic JIA patients. Our aim was to characterize and compare systemic JIA patients with these complications to a larger cohort of systemic JIA patients. 

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