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Totally anomalous pulmonary venous connection through the right lung and via a “Scimitar” vein to the inferior caval vein

Published online by Cambridge University Press:  19 August 2008

Rakesh Dua ,
Christine McTigue  and
James.L Wilkinson
Rakesh Dua*
Affiliation:
From the Department of Cardiology, Royal Children 's Hospital, Parkville, Melbourne
Christine McTigue
Affiliation:
From the Department of Cardiology, Royal Children 's Hospital, Parkville, Melbourne
James.L Wilkinson
Affiliation:
From the Department of Cardiology, Royal Children 's Hospital, Parkville, Melbourne
*
Dr. Rakesh Dua, Clinical Fellow, Department of Cardiology, Royal Children's Hospital, Flemington Road, Parkville, Melbourne, Victoria 3050, Australia. Tel. (03) 345-5717; Fax. (03) 347-5708.
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Abstract

We report a case of totally anomalous pulmonary venous connection in which the two pulmonary veins from the left lung joined to form a common vein which then passed across the midline into a hypoplastic right lung and, after receiving small veins from the right lung, passed inferiorly, exiting the lung below the hilum as a “scimitar” vein and terminating in the inferior caval vein. A separate pulmonary vein from the right lung passed inferiorly independently and joined the “scimitar” vein before it entered the inferior caval vein. There was an associated hypoplastic left heart syndrome.

Keywords

Totally anomalous pulmonary venous connections“Scimitar” syndromehypoplastic left heart syndrome
Type
Brief Reports
Information
Cardiology in the Young , Volume 3 , Issue 1 , January 1993 , pp. 85 - 87
Copyright
Copyright © Cambridge University Press 1993

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References

Darling, RC, Rothney, WB, Craig, JM.Total pulmonary venous drainage into the right side of heart. Report of 17 autopsied cases not associated with other major cardiovascular anomalies. Lab Invest 1957; 6: 44–46.Google Scholar
Fyler, DC, Buckley, LP, Hollenbrand, WE, Cohn, HE.Report of the New England Regional Infant Cardiac Program. Pediatrics 1980; 65(Suppl): 376–461.Google Scholar
Lima, CO, Valdez-Cruz, LM, Allen, HD.Prognostic value of left ventricular size measured by echocardiography in infants with total anomalous pulmonary venous drainage. Am J Cardiol 1983; 51: 1155–1159.CrossRefGoogle Scholar
Hunt, CE, Rao, S, Moller, JH, Edward, JE.Anomalous pulmonary vein serving as collateral channel in aortic stenosis with hypoplastic left ventricle and endocardial fibroelastosis. Chest 1970; 57: 185–189.CrossRefGoogle ScholarPubMed
Suzuki, K, Doi, S, Oku, K.Hypoplastic left heart syndrome with premature closure of foramen ovale: Report of unusual type of total anomalous pulmonary venous return. Heart Vessel 1990; 57: 117–119.CrossRefGoogle Scholar
LeBlanc, JG, Patterson, MW, Taylor, GP, Ashmase, PG.Total anomalous pulmonary venous return with left heart hypoplasia. J Thorac Cardiovasc Surg.1988; 95: 540–542.CrossRefGoogle ScholarPubMed
Seliem, MA, Chin, AJ, Norwood, MI.Patterns of anomalous pulmonary venous connections'drainage in Hypoplastic left heart syndrome. Diagnostic role of Doppler color mapping and surgical implications. J Am Coll Cardiol. 1992; 19: 135–141.CrossRefGoogle ScholarPubMed
Brenner, JI, Bharati, S, Berman, MA, Lev, M.Rare type of intrapulmonary drainage of one lung by the other with total anomalous pulmonary venous return. J Am Coil Cardiol 1983; 2:1174–1177.CrossRefGoogle Scholar
Everhart, FJ, Korns, ME, Amplatz, Kurt, Edwards, JE.Intrapulmonary segment in anomalous pulmonary venous connection. Circulation 1967; 35: 1163–1169.CrossRefGoogle ScholarPubMed
Neil, CA, Ferencz, C, Sabiston, DC, Sheldon, H.The familial occurrence of hypoplastic right lung with systemic arterial supply and venous drainage: “scimitar” syndrome. Bull Johns Hopkins Hospital 1960; 107:1–21.Google Scholar