期刊
INTERNAL MEDICINE
卷 58, 期 7, 页码 965-968出版社
JAPAN SOC INTERNAL MEDICINE
DOI: 10.2169/internalmedicine.1384-18
关键词
idiopathic pulmonary fibrosis; pulmonary hypertension; nintedanib
The patient was a 71-year-old man with severe idiopathic pulmonary fibrosis (IPF) and who demonstrated a slow deterioration of his respiratory condition. After nintedanib administration, his forced vital capacity and chest high-resolution computed tomography (HRCT) findings were stable, but his dyspnea on exertion were worsened. He was diagnosed with pulmonary hypertension (PH) by right heart catheterization (mean pulmonary arterial pressure: 30 mmHg). In this case, we suspected that nintedanib caused his PH, as his IPF had not progressed.
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