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Diaphragmatic eventration as a first sign of Scimitar syndrome

Part of: Cardiac Morphology

Published online by Cambridge University Press:  04 May 2021

Miguel Vieira Martins Open the ORCID record for Miguel Vieira Martins [Opens in a new window] ,
Duarte S Martins  and
Graça Oliveira
Miguel Vieira Martins*
Affiliation:
Pediatrics Department, Centro Hospitalar Universitario Cova da Beira, Covilha, Portugal
Duarte S Martins
Affiliation:
Pediatric Cardiology Department, Hospital Santa Cruz, Centro Hospitalar Lisboa Ocidental, Carnaxide, Portugal
Graça Oliveira
Affiliation:
Neonatology Department, Hospital Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Lisboa, Portugal
*
Author for correspondence: Miguel Vieira Martins, M.D., Pediatrics Department, Centro Hospitalar Universitario Cova da Beira, Quinta do Alvito, 6200-251Covilha, Castelo Branco, Portugal. Tel: +351 275 330 000. E-mail:[email protected]
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Abstract

Diaphragmatic eventration is an anomaly of the diaphragm. In Scimitar syndrome, a curved-shaped anomalous pulmonary venous drainage is seen. Association between these conditions is rare. We present a newborn with diaphragmatic eventration, whose diagnosis of Scimitar syndrome was made after surgical repair. Scimitar syndrome is a congenital disorder often associated with other heart and lungs anomalies. Diagnosis can be fortuitous but with important prognostic features.

Keywords

Congenital diaphragmatic defectsScimitar syndromeNewborn
Type
Brief Report
Information
Cardiology in the Young , Volume 31 , Issue 11 , November 2021 , pp. 1870 - 1872
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Copyright
© The Author(s), 2021. Published by Cambridge University Press

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References

Yang, CK, Shih, JC, Hsu, WM, et al. Isolated right diaphragmatic eventration mimicking congenital heart disease in utero. Prenat Diagn 2005; 25: 872–875. doi: 10.1002/pd.1281.CrossRefGoogle ScholarPubMed
Groth, SS, Andrade, RS Diaphragmatic Eventration. Thorac Surg Clin 2009; 19: 511–519. doi: 10.1016/j.thorsurg.2009.08.003.CrossRefGoogle ScholarPubMed
Clements, BS, Warner, JO The crossover lung segment: congenital malformation associated with a variant of scimitar syndrome. Thorax 1987; 42: 417–419.10.1136/thx.42.6.417CrossRefGoogle ScholarPubMed
Çiçek, S, Arslan, AH, Ugurlucan, M, Yildiz, Y, Ay, S Scimitar syndrome: The curved Turkish sabre. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu 2014; 17: 56–61. doi: 10.1053/j.pcsu.2014.01.003.CrossRefGoogle ScholarPubMed
Gonen, KA, Canitez, Y, Bostan, OM, Yazici, Z Horseshoe lung associated with scimitar syndrome. BMJ Case Rep 2019; 12: 10–13. doi: 10.1136/bcr-2014-204389.CrossRefGoogle ScholarPubMed
Wang, H, Kalfa, D, Rosenbaum, MS, et al. Scimitar Syndrome in Children and Adults: Natural History, Outcomes, and Risk Analysis. Ann Thorac Surg 2018; 105: 592–598. doi: 10.1016/j.athoracsur.2017.06.061.CrossRefGoogle ScholarPubMed