Gastric pneumatosis: a radiological diagnosis with a wide clinical spectrum

Abstract

We present the case of a 72-year-old woman with a history of type 2 diabetes, ischemic stroke, and fracture of the femur. She presented to the emergency department with a 3-day history of vomiting and epigastric pain. Her physical examination was remarkable only for a distended but nonpainful abdomen. She had a mild leucocytosis (11.3×109/L) and elevated C-reactive protein (113mg/L). Radiographs of her chest (● Fig.1) and abdomen (● Fig.2) showed intramural gas in the gastric wall, a pneumoperitoneum, and massive esophageal dilatation. These findings were also observed in a subsequent abdominal computed tomography (CT) scan (● Fig.3). Given the lack of systemic toxicity shewas admitted to the ward for conservative therapy and was kept nil by mouth with intravenous hydration and proton pump inhibitor (PPI) therapy. She did not start antibiotic therapy and blood cultures were negative. She underwent an upper gastrointestinal endoscopy, which showed erosions of the antral mucosa (● Fig.4) with Helicobacter pylori-negative chronic gastritis on histology. A significant reduction of the gastric gas with disappearance of the pneumoperitoneum was documented on a repeat CT scan on day 4.The patient recovered rapidly and was discharged after 1 week. She has been asymptomatic ever since. Gastric pneumatosis is a rare radiological sign that indicates a clinical disorder with a wide spectrum of severity, which ranges from the frequently fatal emphysematous gastritis to oligosymptomatic gastric emphysema. This case is interesting as it clearly illustrates the more benign end of the spectrum of gastric pneumatosis, which can range from this to a fulminating septic condition [1], with subacute presentations in between these extremes [2]. We feel that it is important to manage patients according to the whole clinical picture and not rely solely on imaging findings–even in the presence of traditionally ominous free intraperitoneal gas [3], which proved to be benign in our patient’s case.