肺动脉异常起源地肺动脉闭锁(PA)

Razina Jubada, None Khaleda Parvin Rekha, None Md Mofazzal Sharif, None S M Aftab-E-Alam
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引用次数: 0

摘要

肺动脉闭锁合并室间隔缺损是一种严重的先天性紫绀型心脏病,但并不常见。这里的主肺不是由总动脉干产生的。在肺闭锁中,没有适当的肺瓣膜形成,使血液从心脏流向肺部。不是打开和关闭瓣膜,而是形成一层固体组织。因此,血液不能按照正常的路径从肺部吸收氧气。相反,不足的血液通过心脏及其动脉内的其他自然途径进入肺部,并表现出肺闭锁或动脉不连续的程度。MDCT给出了这方面的结构细节。因此,多层螺旋ct在评估闭锁患者术前手术策略评估所需的详细信息方面发挥着重要作用。我们在此讨论一例肺动脉异常起源的肺动脉闭锁(PA)。KYAMC学报,第14卷,第02期,2023年7月:102-104。
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Pulmonary Atresia (PA) with Anomalous Origin of the Pulmonary Artery
Pulmonary atresia with ventricular septal defect is a severe form of congenital cyanotic heart disease (TOF) but its not very common form. Here main pulmonary does not arises from common arterial trunk. In pulmonary atresia there is no proper formation ofthe pulmonary valve which allows blood from the heart to thelung of patient. Instead of opening and closing of the valve,a solid sheet of tissue develops. Therefore blood cannot flow by its normal path to take oxygen from the lung. Instead, inadequate blood travels to the lung through other natural routes within the heart and its arteries and presenting degree of pulmonary atresia or discontinuity in arteries. MDCT gave structural details in this regard. So, role of MDCT play an important role to evaluate the details important information needed in preoperative evaluation for surgical policy in atretic patients. Here we discuss a case of pulmonary atresia (PA) with anomalous origin of the pulmonary artery.KYAMC Journal Vol. 14, No. 02, July 2023: 102-104.
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