Abstract

Introduction: About 1% of paraesophageal hernias (PEH) require emergency surgery due to obstruction or gangrene. We present two complicated cases of incarcerated PEH.Presentation of cases: A patient aged 18 with trisomy 21 was admitted after four days of vomiting and epigastric pain. CT scan revealed a large PEH. The stomach was massively dilated with compression of adjacent viscera and the celiac trunk. The stomach was repositioned laparoscopically and deflated by endoscopy in an attempt to avoid resection. During second look laparoscopy a gastrectomy was necessary. The patient was reoperated for intestinal obstruction, and treated for dehiscence of the esophagojejunostomy and a pancreatic fistula. A patient aged 65 with hereditary spastic paresis had two days history of emesis and epigastric pain. Upon arrival he was hemodynamically unstable and a CT scan revealed perforation of the herniated stomach. A subtotal gastrectomy without reconstruction was performed with vacuum closure of the abdomen. Later a gastrectomy was completed with a Roux-en-Y reconstruction. Except from reoperation for wound dehiscence after 14 days, the recovery was uneventful.Discussion: Trisomy 21 and hereditary spastic paresis may increase the risk of developing PEH. Challenges in regard to symptom evaluation may delay diagnosis. The pressure of the dilated stomach can give rise to ischemic and mechanical damage from compression of major blood vessels and organs. Urgent diagnosis and gastric deflation is required.Conclusions: In patients with known PEH or with comorbidity that may increase the risk of PEH, this diagnosis should be considered early on.

Highlights

  • About 1% of paraesophageal hernias (PEH) require emergency surgery due to obstruction or gangrene

  • In patients with known PEH or with comorbidity that may increase the risk of PEH, this diagnosis should be considered early on

  • Pooled estimates reveal that 9.2% of patients acutely admitted with PEH obstruction may have incarceration with gangrene [1]

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Summary

Introduction

The prevalence of paraesophageal hernia (PEH) is unknown as many are asymptomatic. Typical manifestations include gastroesophageal reflux, food retention, aspiration pneumonia, and epigastric pain. Pooled estimates reveal that 9.2% of patients acutely admitted with PEH obstruction may have incarceration with gangrene [1]. The annual probability of developing symptoms requiring acute surgery for patients with PEH was 1.2% [2]. The overall 30 and 90-day mortality in emergency cases in a cohort of 12,441 patients was 7% and 11.5%, respectively [1]. In case of obstruction emergent intervention is required. In some patients early diagnosis, may be challenging and adequate treatment could be delayed. We. report two patients, one with trisomy 21 and another with hereditary spastic paresis who were treated for incarcerated PEH at our Institute. The work has been reported in line with the SCARE criteria and the PROCESS CHECKLIST [3,4]

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