Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results

Journal

2014 | 9 | 3 | 508-512

Article title

Delayed diagnosis of an isolated partial anomalous pulmonary venous connection

Content

Title variants

Languages of publication

EN

Abstracts

EN
In this case report we describe the delayed diagnosis of a very rare congenital anomaly - isolated partial anomalous pulmonary venous connection. This congenital anomaly should be suspected at any age in the clinical setting of right heart volume overload, especially in the absence of a large atrial septal defect. Tomographic imaging modalities (computed tomography or cardiovascular magnetic resonance) not only allow the comprehensive structural and functional assessment of this anomaly, but also help assess the patient’s suitability for surgical treatment. Surgery is the definitive treatment of a patient with a significant left-to-right shunt due to partial anomalous pulmonary venous connection.

Publisher

Journal

Year

Volume

9

Issue

3

Pages

508-512

Physical description

Dates

published
1 - 6 - 2014
online
8 - 7 - 2014

Contributors

  • Department of Radiology, Nuclear Medicine and Physics of Medicine, Vilnius University, Vilnius, Lithuania
  • Department of Radiology, Nuclear Medicine and Physics of Medicine, Vilnius University, Vilnius, Lithuania

References

  • [1] Katre R., Burns S.K., Murillo H., Lane M.J., Restrepo C.S., Anomalous pulmonary venous connections, Semin Ultrasound CT MR, 2012, 33(6), 485–499 http://dx.doi.org/10.1053/j.sult.2012.07.001[Crossref]
  • [2] Demos T.C., Posniak H.V., Pierce K.L., Olson M.C., Muscato M., Venous anomalies of the thorax, AJR Am J Roentgenol, 2004, 182(5), 1139–1150 http://dx.doi.org/10.2214/ajr.182.5.1821139[Crossref]
  • [3] Van Meter C.J., LeBlanc J.G., Culpepper W.S., Ochsner J.L., Partial anomalous pulmonary venous return, Circulation, 1990, 82(5 Suppl), IV195–198 [WoS]
  • [4] Posniak H.V., Dudiak C.M., Olson M.C., Computed tomography diagnosis of partial anomalous pulmonary venous drainage, Cardiovasc Intervent Radiol, 1993, 16(5), 319–320 http://dx.doi.org/10.1007/BF02629166[Crossref]
  • [5] Dillon E.H., Camputaro C., Partial anomalous pulmonary venous drainage of the left upper lobe vs duplication of the superior vena cava: distinction based on CT findings, AJR Am J Roentgenol, 1993, 160(2), 375–379 http://dx.doi.org/10.2214/ajr.160.2.8424355[Crossref]
  • [6] Fulton D.R., Soriano B., Partial anomalous pulmonary venous connection, UpToDate database, 2013, http://www.uptodate.com/contents/partial-anomalous-pulmonary-venous-connection
  • [7] Senocak F., Ozme S., Bilgic A., Ozkutlu S., Ozer S., Saraclar M., Partial anomalous pulmonary venous return: evaluation of 51 cases, Jpn Heart J, 1994, 35(1), 43–50 http://dx.doi.org/10.1536/ihj.35.43[Crossref]
  • [8] Young T.W., Anomalous pulmonary veins return, In: Moodie D.S. (Ed.), Clinical management of congenital heart disease from infancy to adulthood, 1st ed., Cardiotext Publishing, Minneapolis, 2013
  • [9] Clarke J.C., Aragam J.R., Bhatt D.L., Brown J.D., Ferrazzani S., Pietro D.A., Maron B.A., An unusual cause of dyspnea diagnosed late in life: severe pulmonary hypertension resulting from isolated anomalous pulmonary venous connection, Circ Cardiovasc Imaging, 2013, 6(2), 349–351 http://dx.doi.org/10.1161/CIRCIMAGING.112.000145[WoS][Crossref]
  • [10] Kim T.H., Kim Y.M., Suh C.H., Cho D.J., Park I.S., Kim W.H., Lee Y.T., Helical CT angiography and three-dimensional reconstruction of total anomalous pulmonary venous connections in neonates and infants, AJR Am J Roentgenol, 2000, 175(5), 1381–1386 http://dx.doi.org/10.2214/ajr.175.5.1751381[Crossref]
  • [11] Schwitter J. (Ed.), CMR update, 2nd ed., Kueng Druck AG, Switzerland, 2012

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_s11536-013-0312-0
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.