Vanishing spleen after Nissen fundoplication: a case report
Nissen fundoplication is a generally accepted treatment for severe gastro-oesophageal reflux after conservative management has failed. The surgical techniques and the complications that may develop following the operation have been well described. However, necrosis of the spleen is a rare complicati...
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Veröffentlicht in: | European journal of pediatrics 2009-03, Vol.168 (3), p.355-357 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Nissen fundoplication is a generally accepted treatment for severe gastro-oesophageal reflux after conservative management has failed. The surgical techniques and the complications that may develop following the operation have been well described. However, necrosis of the spleen is a rare complication. We report here a patient with Down syndrome with a vanishing spleen after a Nissen fundoplication, who died of overwhelming pneumococcal septic shock 7 months after the operation. Vascular anomaly in Down syndrome, inadvertent ligation of the splenic artery or volvulus of the spleen may have caused a compromised splenic arterial circulation.
Conclusion
Nissen fundoplication may be associated with vanishing spleen and, consequently, with devastating consequences. |
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ISSN: | 0340-6199 1432-1076 |
DOI: | 10.1007/s00431-008-0752-8 |