Hemorrhagic Shock: A Meckel Diverticulum Rare Presentation

Date of submission: 05-05-2019 | Date of acceptance: 20-12-2019 | Published: 02-04-2020

Authors

  • Mariana Morgado Pediatric Surgery Department, Centro Hospitalar Lisboa Norte, Hospital de Santa Maria, Portugal
  • Filipa Jalles Pediatric Surgery Department, Centro Hospitalar Lisboa Norte, Hospital de Santa Maria, Portugal
  • Miroslava Gonçalves Pediatric Surgery Department, Centro Hospitalar Lisboa Norte, Hospital de Santa Maria, Portugal

DOI:

https://doi.org/10.25754/pjp.2020.17757

Abstract

Meckel’s diverticulum is the most frequent congenital malformation of the gastrointestinal tract. The diagnosis is challenging and often incidental, because it is infrequently symptomatic. Symptomatic presentation is more common in the first decade of life and complications are more prevalent in the first 2 years, decreasing afterwards. Complications include ulceration with haemorrhage, perforation, bowel occlusion and neoplasm. We report a clinical case of a rare Meckel’s diverticulum presentation, in an adolescent, with haemorrhagic shock and we make a brief literature review.

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Published

2020-04-17

Issue

Section

Case reports

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