Reconstruction of bilateral branch pulmonary artery stenosis caused by Takayasu's aortitis.
Reconstruction of bilateral branch pulmonary artery stenosis caused by Takayasu's aortitis.
复制标题
高安主动脉炎所致双侧肺动脉分支狭窄的重建。
DOI：
10.1253/circj.68.791
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发表时间：
2004
期刊：
影响因子：
--
通讯作者：
J. Matsubara
中科院分区：
文献类型：
--
作者：
H. Shikata;S. Sakamoto;Y. Ueda;S. Tsuchishima;T. Matsubara;H. Nishizawa;S. Shono;M. Kanno;Takashi Shimizu;J. Matsubara
A 63 year-old female presented with dyspnea on exertion. Her chest X-ray showed cardiomegaly, and right ventricular overload and tricuspid regurgitation were detected. Her pulmonary ventilation and blood flow scintigraphy findings were suspicious of pulmonary vascular disease; the diagnosis was pulmonary hypertension and bilateral branch pulmonary artery stenosis. After the inflammation settled, the stenotic bilateral branch pulmonary artery was reconstructed with a prosthetic vessel and the pulmonary pressure normalized immediately. A resected specimen revealed that the stenotic changes were from Takayasu's disease. The patient's postoperative course was uneventful, and pulmonary ventilation and blood scintigraphy returned to an almost normal range. At follow-up 5 years and 6 months after the operation, there was no evidence of pulmonary artery disease (eg, stenosis and/or ischemia) or of any change in the central vessels of the retina, the so-called Takayasu's retinopathy.
