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Updated: Jun 4, 2025

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婴儿期肺高血压:一个可逆的原因

Cassandra Campbell1, Kawaljeet Singh2, Mark Weems2

  • 1Pediatrics, The University of Tennessee Health Science Center, Memphis, Tennessee, USA cassie.devol@gmail.com.

BMJ case reports
|January 3, 2025
PubMed
概括

一种罕见的先天性心脏缺陷 - - 上心膜环 - - 在婴儿身上引起严重的肺高血压. 手术切除膜成功治疗了这种情况,强调了准确诊断的重要性.

关键词:
遗传性疾病 遗传性疾病肺高血压是一种肺高血压.膜疾病 膜疾病

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Pulmonary hypertension (PH) is a severe health condition in which the mean pulmonary arterial pressure increases to 25 mmHg or more, even when the body is at rest. This high pressure in the blood vessels that transport blood from the heart to the lungs can cause various symptoms, including shortness of breath, can lead to right heart failure, and significantly affect the overall quality of life.
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Receptor tyrosine kinase inhibitors (TKIs) and calcium channel blockers (CCBs) are two critical categories of drugs employed in the treatment of pulmonary artery hypertension (PAH). PAH is a disease that causes high blood pressure in the pulmonary arteries, resulting in chest pain, fatigue, and shortness of breath.
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