Splenic torsion after congenital diaphragmatic hernia repair: Case report and review of the literature

Anupama Mehta, Paul Geoffrey Vana*, Loretto Glynn

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Wandering spleen with torsion, a rare clinical diagnosis, was found to be the cause of chronic abdominal pain in an 11-year-old female with a history of congenital diaphragmatic hernia repaired at three days of age. Doppler ultrasound revealed patent vessels with splenomegaly, and computed tomography (CT) showed an absence of the spleen in the left subphrenic space with torsion at the splenic hilum. Due to the chronicity of pain and risk of ischemia from torsion, open splenopexy with Vicryl mesh was performed. This case report/review of the literature discusses the rarity of this condition, and the importance of timely diagnosis and intervention.

Original languageEnglish (US)
Pages (from-to)E29-E31
JournalJournal of pediatric surgery
Volume48
Issue number3
DOIs
StatePublished - Mar 2013

Keywords

  • Congenital diaphragmatic hernia
  • Splenic torsion
  • Splenopexy
  • Wandering spleen

ASJC Scopus subject areas

  • Surgery
  • Pediatrics, Perinatology, and Child Health

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