Rare case of Ischaemic Meckel’s diverticulum in spigelian hernia

Authors

  • Tahmina Hakim Department of General Surgery, Campbelltown Hospital, New South Wales, Australia
  • Selwyn Selvendran Department of General Surgery, Campbelltown Hospital, New South Wales, Australia
  • Soumya Hariswamy Department of General Surgery, Campbelltown Hospital, New South Wales, Australia
  • Neha Gauri Department of General Surgery, Campbelltown Hospital, New South Wales, Australia
  • Edward Tong Department of General Surgery, Campbelltown Hospital, New South Wales, Australia

DOI:

https://doi.org/10.18203/2349-2902.isj20253035

Keywords:

Bowel obstruction, Meckel’s diverticulitis, Spigelian hernia

Abstract

Ischemic Meckel’s diverticulum in Spigelian hernia is a rare condition and poses a significant diagnostic and management challenges. Spigelian hernia is a rare type of acquired ventral hernia that accounts for 1-2% of all abdominal wall hernias. We present a rare case of a 59-year-old female patient who presented with incarcerated abdominal wall hernia. The preoperative CT scan showed left sided abdominal wall hernia and not bowel obstruction. However, intra-operatively patient had an ischaemic small bowel segment and a necrotic Meckel’s diverticulum in Spigelian hernia. The patient underwent a laparoscopic procedure converted to open repair of spigelian hernia with resection of small bowel containing ischaemic Meckel’s diverticulum.  Patient’s post-operative recovery course was unremarkable and diet was gradually upgraded. Incarcerated/ischaemic Meckel’s diverticulum in a Spigelian hernia is rare and may present with significant pre-operative diagnostic challenges. CT or MRI could be helpful diagnostic modalities. Both open or laparoscopic repairs could be performed depending on clinical situations.

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References

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Published

2025-09-25

How to Cite

Hakim, T., Selvendran, S., Hariswamy, S., Gauri, N., & Tong, E. (2025). Rare case of Ischaemic Meckel’s diverticulum in spigelian hernia. International Surgery Journal, 12(10), 1806–1808. https://doi.org/10.18203/2349-2902.isj20253035

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Section

Case Reports