Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-17T14:43:18.792Z Has data issue: false hasContentIssue false
  • English
  • Français

Bilateral scimitar syndrome

Published online by Cambridge University Press:  21 January 2005

Mohamed Kabbani ,
Naser Haider  and
Riyadh Abu-Sulaiman
Mohamed Kabbani
Affiliation:
Cardiac Sciences Department, King Abdul Aziz Medical City, Riyadh, Saudi Arabia
Naser Haider
Affiliation:
Pediatric Department, King Abdul Aziz Medical City, Riyadh, Saudi Arabia
Riyadh Abu-Sulaiman
Affiliation:
Pediatric Department, King Abdul Aziz Medical City, Riyadh, Saudi Arabia
Get access Rights & Permissions [Opens in a new window]

Abstract

Scimitar syndrome is a rare congenital anomaly that affects classically the right lung and the heart. We present a rare variant that involves both lungs in association with totally anomalous pulmonary venous connection, horseshoe lung, and right pulmonary cyst.

Keywords

Horseshoe lungtotally anomalous pulmonary venous connectionpulmonary cyst
Type
Brief Report
Information
Cardiology in the Young , Volume 14 , Issue 4 , August 2004 , pp. 447 - 449
Copyright
© 2004 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Mordue BC. A case series of five infants with scimitar syndrome. Adv Neonatal Care 2003; 3: 121–132.Google Scholar
Rutledge JM, Hiatt PW, Wesley Vick III G, Grifka RG. A sword for the left hand: an unusual case of left-sided scimitar syndrome. Pediatr Cardiol 2001; 22: 350–352.Google Scholar
Kamijoh M, Itoh M, Kikimoto C, Nagakaura T, Okabe T. Horseshoe lung with bilateral vascular anomalies: a rare variant of hypogenetic lung syndrome (scimitar syndrome). Pediatr Int 2002; 44: 443–445.Google Scholar
Gilkeson RC, Lee JH, Sachs PB, Clampitt M. Gadolnium-enhanced magnetic resonance angiography in scimitar syndrome: diagnosis and postoperative evaluation. Tex Heart Inst J 2000; 27: 309–311.Google Scholar
Puvaneswary M, Leitch J, Chard RB. MRI of partial anomalous pulmonary venous return (scimitar syndrome). Australia Radiol 2003; 47: 92–93.Google Scholar
Najm HK, Williams WG, Coles JG, Rebeyka IM, Freedom RM. Scimitar syndrome: twenty years experience and results of repair. J Thorac Cardiovasc Surg 1996; 112: 1161–1169.Google Scholar
Gao YA, Burrows PE, Benson LN, Rabinovitch M, Freedom RM. Scimitar syndrome in infancy. J Am Col Cardiol 1993; 22: 873–882.Google Scholar