Thorac Cardiovasc Surg 2001; 49(6): 378-379
DOI: 10.1055/s-2001-19012
Case Report
© Georg Thieme Verlag Stuttgart · New York

Bidirectional Glenn Shunt in
an Infant with Prune-Belly
Syndrome

R.  Doğan1 , M.  Yılmaz1 , Ü.  Duman1 , S.  Özkutlu2
  • 1Department of Thoracic and Cardiovascular Surgery,
    Hacettepe University, Faculty of Medicine, Ankara, Turkey
  • 2Department of Paediatric Cardiology, Hacettepe University, Faculty of Medicine, Ankara, Turkey
Further Information

Publication History

Publication Date:
17 December 2001 (online)

The prune-belly syndrome (PBS) usually is described as a deficiency of the anterior abdominal muscle involving bilateral cryptorchidism and urinary tract malformations. In this report, we will present an eleven-month-old boy with PBS associated with a complex cardiac anomaly. A bilateral bidirectional Glenn shunt was performed with the diagnosis of isolated dextrocardia, single ventricle, pulmonary atresia, incomplete A-V septal defect, hemiazygos continuity, persistent right superior vena cava, patent ductus arteriosus-dependent pulmonary blood flow. The patient required special consideration for postoperative pulmonary care.

References

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Received for Publication: March 26, 2001

Prof. Rıza Doğan, MD 

Department of Thoracic and Cardiovascular Surgery
Hacettepe University, Faculty of Medicine

06100 Ankara, Turkey

Phone: 90 (312) 311-73 77

Fax: 90 (312) 311-09 95

Email: rdogan@hacettepe.edu.tr

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