Misumi Kayo, Ogo Takeshi, Ueda Jin, Tsuji Akihiro, Fukui Sigefumi, Konagai Nao, Asano Ryotaro, Yasuda Satoshi
Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, Japan.
Department of Advanced Medicine in Pulmonary Hypertension, National Cerebral and Cardiovascular Center, Japan.
Intern Med. 2019 Feb 1;58(3):395-399. doi: 10.2169/internalmedicine.1523-18. Epub 2018 Sep 12.
Pulmonary arterial hypertension (PAH) is a rare, devastating disease, characterized by elevated pulmonary arterial pressure due to pulmonary microvascular obstruction, which can result in heart failure and death. PAH can be associated with exposure to certain drugs or toxins. We herein report a case in which PAH developed in a patient with refractory ulcerative colitis during treatment with "Qing-Dai," a Chinese herbal medicine. The patient's PAH improved after the discontinuation of Qing-Dai.
肺动脉高压(PAH)是一种罕见的、具有毁灭性的疾病,其特征是由于肺微血管阻塞导致肺动脉压力升高,可导致心力衰竭和死亡。PAH可能与接触某些药物或毒素有关。我们在此报告一例在用中药“青黛”治疗难治性溃疡性结肠炎患者期间发生PAH的病例。停用青黛后,患者的PAH有所改善。