# An Injection Leading to Oesophageal Perforation: A Rare Case of Contained Boerhaave’s Syndrome Following Unsupervised GLP-1/GIP Receptor Agonist Dose Escalation

**Authors:** Noor Sadiq Syed, Thomas Oldfield, Syed Akash-Ul-Husnain, Atif Moiz

PMC · DOI: 10.7759/cureus.101811 · Cureus · 2026-01-18

## TL;DR

An 18-year-old woman developed a rare contained oesophageal perforation after self-escalating GLP-1/GIP receptor agonist doses, managed successfully without surgery.

## Contribution

Reports a rare case linking unsupervised GLP-1/GIP therapy to oesophageal injury and conservative management success.

## Key findings

- Self-escalation of GLP-1/GIP agonist led to severe vomiting and contained oesophageal perforation.
- Conservative treatment with IV antibiotics and fluids successfully managed the injury.
- Imaging showed pneumothorax and mediastinal emphysema without contrast extravasation, indicating spontaneous sealing.

## Abstract

Oesophageal perforation, also known as Boerhaave’s syndrome, is a rare but potentially fatal condition that classically results from forceful emesis. Prompt diagnosis is critical, as delays are associated with a significant increase in morbidity and mortality. We present the case of an 18-year-old woman who developed severe and persistent vomiting after self-escalation of a dual glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) receptor agonist prescribed for weight loss, culminating in a contained oesophageal perforation. Imaging demonstrated a pneumothorax and extensive mediastinal emphysema (pneumomediastinum), without evidence of ongoing contrast extravasation on water-soluble swallow, suggesting spontaneous sealing of the perforation. The patient was successfully managed conservatively on a medical ward with intravenous (IV) antibiotics, IV fluids, proton pump inhibitor (PPI) therapy, and close clinical observation.

This case highlights the importance of recognising severe vomiting associated with GLP-1/GIP receptor agonist therapy as a potential precipitant of oesophageal injury and demonstrates that carefully selected contained perforations may be successfully managed conservatively with close multidisciplinary monitoring.

## Linked entities

- **Diseases:** Boerhaave’s syndrome (MONDO:0022013)

## Full-text entities

- **Genes:** GIP (gastric inhibitory polypeptide) [NCBI Gene 2695], GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** sepsis (MESH:D018805), emesis (MESH:D014839), rigidity (MESH:D009127), chest pain (MESH:D002637), effects (MESH:D065606), perforations (MESH:D057112), epigastric tenderness (MESH:D063806), appetite (MESH:D001068), pleural effusions (MESH:D010996), hematemesis (MESH:D006396), pneumomediastinum (MESH:D008478), nausea (MESH:D009325), leaks (MESH:D019559), weight loss (MESH:D015431), Oesophageal Perforation (MESH:D000077277), emphysema (MESH:D004646), Boerhaave's Syndrome (MESH:C536571), inflammatory response (MESH:D018746), oesophageal rupture (MESH:D012421), Gastrointestinal adverse effects (MESH:D005767), pneumothorax (MESH:D011030), alcohol misuse (MESH:D000437), melena (MESH:D008551), abscesses (MESH:D000038), inflammatory (MESH:D007249), dysphagia (MESH:D003680)
- **Chemicals:** Water (MESH:D014867), piperacillin-tazobactam (MESH:D000077725), oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

7 references — full list in the complete paper: https://tomesphere.com/paper/PMC12914087/full.md

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Source: https://tomesphere.com/paper/PMC12914087