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Patients with pediatric rheumatic disease rarely develop pulmonary arterial hypertension (PAH), and the expected prognosis had been very poor. With the advancement of oral medicine for PAH in recent years, we can expect better prognosis of these patients. For this purpose, early diagnosis and interventions are essential.

pediatric rheumatology online journal

PReS-FINAL-2267: Successful treatment of pulmonary arterial hypertension associated with connective tissue disease (PAH-CTD) with combination therapy of sildenafil and ambrisentan: a case report