# A Rare but Lethal Emergency: A Case Report on Boerhaave’s Syndrome

## TL;DR

This case report describes a rare and life-threatening condition called Boerhaave's syndrome, highlighting the importance of early diagnosis and surgical treatment for better outcomes.

## Contribution

The paper presents a clinical case emphasizing the diagnostic challenges and management of Boerhaave's syndrome.

## Key findings

- Boerhaave's syndrome was diagnosed in a 71-year-old female through contrast-enhanced computed tomography.
- Emergency thoracotomy and esophageal repair improved patient outcomes.
- Early diagnosis and multidisciplinary management are critical for reducing mortality.

## Abstract

Boerhaave's syndrome is a rare and life-threatening condition characterized by spontaneous esophageal rupture, often precipitated by sudden increases in intra-esophageal pressure, typically following forceful vomiting. The nonspecific nature of its clinical presentation, which may include chest pain, vomiting, and dyspnea, often overlaps with other thoracic or gastrointestinal disorders, making diagnosis challenging. This case report describes a 71-year-old female who presented with acute chest pain following episodes of vomiting. Initial clinical examination revealed tachycardia, tachypnea, and subcutaneous emphysema, raising suspicion of Boerhaave's syndrome. Diagnosis was confirmed through contrast-enhanced computed tomography (CECT), which revealed a 3 cm perforation in the thoracic esophagus with pleural effusion.

The patient was managed surgically with emergency thoracotomy, debridement, primary esophageal repair reinforced with an intercostal muscle flap, and the placement of a feeding jejunostomy. This case underscores the importance of early diagnosis, prompt surgical intervention, and multidisciplinary management in mitigating the high mortality associated with Boerhaave's syndrome.