# Spontaneous Pneumomediastinum and Cannabinoid Hyperemesis Syndrome: A Case Report and Literature Review

**Authors:** Baqir Jafry, Shawn Chillag

PMC · DOI: 10.7759/cureus.101979 · Cureus · 2026-01-21

## TL;DR

An 18-year-old man with chronic marijuana use developed chest and abdominal pain due to a rare condition linked to vomiting, highlighting a new connection between cannabis use and a specific medical issue.

## Contribution

This case report adds to the limited literature on the association between cannabinoid hyperemesis syndrome and spontaneous pneumomediastinum.

## Key findings

- The patient had chronic marijuana use and developed spontaneous pneumomediastinum after forceful vomiting.
- Only five cases link cannabinoid hyperemesis syndrome to spontaneous pneumomediastinum.
- Conservative management was effective for the patient's condition.

## Abstract

We report the case of an 18-year-old man with a six-month history of chronic marijuana use who developed spontaneous pneumomediastinum (SPM) following multiple episodes of forceful vomiting. He presented with chest pain, shortness of breath, and abdominal pain radiating to the back. A noncontrast chest CT revealed a small amount of mediastinal air without evidence of esophageal perforation, which was confirmed with a CT esophagram. He was managed conservatively with bowel rest, IV antibiotics, and supportive care. This case is one of only five to date recognizing the association between cannabinoid hyperemesis syndrome (CHS) and SPM and highlights a relatively benign condition that may not be considered in the differential diagnosis because of an uncommon underlying cause. The pathophysiology, management, and outcomes of CHS-induced SPM are discussed to place this case in context.

## Linked entities

- **Diseases:** cannabinoid hyperemesis syndrome (MONDO:0100094)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** nausea (MESH:D009325), tachycardia (MESH:D013610), respiratory deterioration (MESH:D012131), SPM (MESH:D008478), chest pain (MESH:D002637), pulmonary embolism (MESH:D011655), hypotension (MESH:D007022), metabolic abnormalities (MESH:D008659), tears (MESH:D012167), alveolar (MESH:D002282), vomiting (MESH:D014839), esophageal leak (MESH:D004941), Mallory-Weiss tear (MESH:D008309), alveolar rupture (MESH:D012421), dyspnea (MESH:D004417), insomnia (MESH:D007319), pancreatitis (MESH:D010195), abdominal pain (MESH:D015746), esophageal perforation (MESH:D004939), mediastinitis (MESH:D008480), tenderness (MESH:D063806), spontaneous (MESH:D005598), infectious (MESH:D003141), dysphagia (MESH:D003680), barotrauma (MESH:D001469), peptic ulcer disease (MESH:D010437), Boerhaave syndrome (MESH:C536571), subcutaneous emphysema (MESH:D013352), CHS (MESH:D006939)
- **Chemicals:** promethazine (MESH:D011398), haloperidol (MESH:D006220), oxygen (MESH:D010100), lactate (MESH:D019344), capsaicin (MESH:D002211), alcohol (MESH:D000438), glucose (MESH:D005947), ondansetron (MESH:D017294), CHS (-), piperacillin-tazobactam (MESH:D000077725)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12922459/full.md

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Source: https://tomesphere.com/paper/PMC12922459