right pulmonary artery

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Related to right pulmonary artery: Left pulmonary artery

right pul·mo·nar·y ar·ter·y

the longer of the two terminal branches of the pulmonary trunk, it passes transversely across the midline in the superior mediastinum, passing inferior to the aortic arch to enter the hilum of the right lung as part of its root. Branches divide and are distributed with the segmental and subsegmental bronchi; frequent variations occur. Typical branches: of the superior lobar arteries [TA] (arteriae lobares superiores pulmonis [TA]) are the apical segmental artery [TA] (arteria segmentalis apicalis pulmonis [TA]), anterior segmental artery (arteria segmentalis anterior pulmonis [TA]) and posterior segmental artery [TA] (arteria segmentalis posterior pulmonis [TA]), with the latter two having ascending and descending branches [TA] (rami ascendens et descendens [TA]); of the middle lobar artery [TA] (arteria lobaris media [TA]) are the medial segmental artery [TA] (arteria lobaris media pulmonis [TA]) and lateral segmental artery [TA] (arteria segmentalis lateralis pulmonis [TA]); and of the inferior lobar arteries [TA] (arteriae lobares inferiores pulmonis [TA]) are the superior segmental artery [TA] (arteria segmentalis superior pulmonis [TA]) and a basal part [TA] (pars basalis [TA]) giving rise to anterior, posterior, lateral, and medial basal segmental arteries [TA] (arteriae segmentales basales anterior, posterior, lateralis et medialis pulmonales [TA]).
Synonym(s): arteria pulmonalis dextra [TA]

right pulmonary artery

the longer and slightly larger of the two arteries conveying venous blood from the heart to the lungs. It arises from the pulmonary trunk, bends to the right behind the aorta, and divides into two branches at the root of the right lung. Compare left pulmonary artery.

right pul·mo·nar·y ar·te·ry

(rīt pul'mŏ-nar-ē ahr'tĕr-ē) [TA]
The longer of the two terminal branches of the pulmonary trunk, it passes transversely across the mediastinum inferior to the aortic arch to enter the hilum of the right lung. Branches are distributed with the bronchi; frequent variations occur. Typical branches to the superior lobe (rami lobi superioris [TA]) are apical (ramus apicalis [TA]), anterior ascending (ramus anterior ascendens [TA]), anterior descending (ramus anterior descendens [TA]), posterior ascending (ramus posterior ascendens [TA]), and posterior descending (ramus posterior descendens [TA]); to the middle lobe (rami lobi medii [TA]) are medial (ramus medialis [TA]) and lateral (ramus lateralis [TA]), and to the inferior lobe (rami lobi inferioris [TA]) are superior (apical) branch of inferior lobe (ramus superior (apicalis) lobi inferioris [TA]), and the anterior, lateral (lateralis), medial (medialis), and posterior basal branches (rami basales).
References in periodicals archive ?
Anomalous origin of the right pulmonary artery from the ascending aorta.
Mitral valve prolapse causing severe mitral regurgitation in a patient with absent right pulmonary artery.
No right pulmonary artery (RPA) branch could be visualised, and there were indications of multiple collateral arteries supplying the lungs.
There was a hypoplastic right pulmonary artery arising from the proximal descending aorta, supplying the right upper lung zone.
6,7,8] The most common lesions associated with APW are the following: aortic origin of the right pulmonary artery, type I interruption of the aortic arch, anomalous origin of the right coronary artery from the pulmonary artery and Tetralogy of Fallot.
Penner C, Maycher B, Light RB: compression of the left main bronchus between a descending thoracic aortic aneurysm and an enlarged right pulmonary artery.
The right ventriculogram showed simultaneous visualization of both pulmonary arteries, overrided aorta from right ventricle, infundibulary stenosis, normally located right pulmonary artery and absence of normal bifurcation of pulmonary trunk and left pulmonary artery (Fig.
Absent right pulmonary artery (ARPA) is rare as an isolated cardiac anomaly, and has a wide variety of clinical presentations, ranging from life-threatening symptoms of congestive heart failure with severe pulmonary hypertension to incidental findings on chest x-ray (CXR).
RPALAF is a direct connection between branches of the right pulmonary artery and left atrium through a thin-walled aneurysm.
Right pulmonary artery to left atrium communication.
Isolated absence of the right pulmonary artery as a cause of massive hemoptysis.
Computed tomography of pulmonary angiogram (CTPA) showed a large filling defect in the right pulmonary artery (PA) and a minimal filling defect in the left PA [[Figure 1], pre-procedure, case 1].