A rare cause of pulmonary hypertension: bilateral pulmonary artery involvement and stent restenosis due to Takayasu arteritis
A 53-year-old female patient was admitted with dyspnea and fatigue. On transthoracic echocardiography, systolic pulmonary artery pressure (PAP) was measured as 90 mmHg, and right heart catheterization revealed pulmonary arterial hypertension. Pulmonary angiography demonstrated bilateral pulmonary ar...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
KARE Publishing,
2014-06-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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