家族性原发性肺动脉高压——两个兄弟姐妹的报告。

K Kodama, M Hamada, Y Shigematsu, M Suzuki, K Hiwada, Y Hayashi, H Hashimoto, H Hashimoto, A Sugita
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引用次数: 2

摘要

家族性原发性肺动脉高压见于两个兄弟姐妹(姐妹和兄弟)。女性在28岁时出现劳累性呼吸困难,弟弟在38岁时出现劳累性呼吸困难、咳带血痰和胫前水肿。根据血流动力学和组织病理学结果,我们诊断为原发性肺动脉高压。无论治疗如何,两名患者都在短时间内死于右侧心力衰竭。我们检查了他们的家庭成员,但没有其他成员患有原发性肺动脉高压。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Familial primary pulmonary hypertension--report of two siblings.

Familial primary pulmonary hypertension was found in two siblings (sister and brother). The woman noted exertional dyspnea at the age of 28 yr. The younger brother noticed exertional dyspnea, cough with bloody sputum and pretibial edema at the age of 38 yr. We diagnosed them as primary pulmonary hypertension as based on hemodynamic and histopathological findings. Regardless of the treatment, both patients died of right-sided heart failure with a short time course. We examined their family members, but there were no other members with primary pulmonary hypertension.

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