Esophagogastroduodenal pneumatosis with subsequent pneumoporta and intramural duodenal hematoma after endoscopic hemostasis: a case report

A 70-year-old male patient presented himself to the emergency department due to having had productive cough for one week. He has a past history of type 2 diabetes mellitus, stage III chronic kidney disease, hypertension, old pulmonary tuberculosis, and poliomyelitis. He also received a mechanical valve replacement for severe tricuspid regurgitation and has been taking warfarin for 10 years. He was admitted with the diagnosis of community-acquired pneumonia, and received amoxicillin/clavulanic acid.

On the second day after admission, the patient developed massive upper gastrointestinal bleeding with a remarkable decrease of hemoglobin from 11.1 g/dL to 7.6 g/dL. He had a profound coagulopathy with prothrombin time (PT) of 43.4 s, international normalized ratio (INR) of 4.07, and activated partial thromboplastin time (aPTT) of 63.2 s. The platelet count was 252,000/μL. Warfarin was discontinued. He received blood component therapy and Vitamin K1 to correct anemia and coagulopathy. He also received intravenous esomeprazole. The panendoscopic examination showed an ulcer on the duodenal bulb with an active oozing vessel on the ulcer crater (Fig. 1-a). Hemostasis was performed with epinephrine injection and hemoclipping (Fig. 1-b).

The patient had abdominal pain, gastrointestinal bleeding and hypotension one day after the endoscopic procedure. Hemoglobin was further dropped to 5.8 g/dL, and coagulopathy was worsened with PT of 60.4 s, INR of 5.69, and aPTT of 60.1 s despite of aggressive component therapy. Total serum bilirubin level was rapidly elevated from 1.68 mg/dL to 6.00 mg/dL. Acute pancreatitis was also suspected with a lipase level of 3743 IU/L. Computed tomography of the abdomen showed a 14.4 cm × 7 cm intramural hematoma at the second portion of duodenum (Fig. 2-a). The stomach was distended which indicated gastric outlet obstruction. He also had air retention in the portal vein and wall of esophagus, stomach and bulb (Fig. 2- b to d).

The patient developed respiratory failure and shock, and he received support with mechanical ventilation. His bleeding tendency was corrected by vitamin K1 and blood component therapy. Hemodynamic instability was promptly resolved within two days. Abdominal ultrasonography taken six days later showed the finding of complete resolution of the duodenal hematoma, and was confirmed with endoscopy two weeks later (Fig. 3). But, his renal function was progressively worsened, and the patient and his family declined hemodialysis therapy. The patient died of renal failure on the 40th day after admission.

Depending on the involved site of gastrointestinal tract, clinical presentation of PI is usually nonspecific, varying from chest pain, diarrhea, constipation, abdominal pain, abdominal distension, nausea, vomiting, to gastrointestinal bleeding, or even no symptom [1, 3, 4].

Gastric pneumatosis has been described in various circumstances, including patients who have hemorrhagic radiation gastritis after Argon plasma coagulation [5], gastric ulcer [6], corrosive injury of stomach, status post endoscopy, gastric outlet obstruction, duodenal obstruction, nasogastric tube placement [3], hepatectomy with vascular reconstruction, obstructive pulmonary disease with bleb rupture [7], and high-dose dexamethasone therapy [8]. It can be divided into two categories: first, gastric emphysema, implying benign condition and usually being managed by conservative treatment; and second, emphysematous gastritis, suggesting emergent condition, and surgical intervention being critical for life-saving. Mclaughlin et al. have proposed to use the term gangrenous PI/nongangrenous PI instead of emphysematous gastritis/gastric emphysema, to avoid misleading [7].

IDH is also a rare condition that mostly occurs after a blunt abdominal trauma because that the duodenum has rich submucosal vascular supply and is fixed in retroperitoneum [9]. IDH has also been reported as clinical finding associated with anticoagulant therapy, blood dyscrasia, pancreatic disease, collagen vascular disease [10], and diagnostic/therapeutic endoscopy [11] such as endoscopic retrograde cholangiopancreatography with sphincterotomy and biliary stone retrieval [12]. It tends to occur in patients with liver cirrhosis, coagulopathy and hemodialysis especially [11]. IDH is usually confined from the first portion to the second portion of the duodenum due to the barrier of pylorus and ligament of Treitz. Typical symptoms of IDH include epigastric pain, vomiting, and hematochezia. Acute pancreatitis is the most frequent comorbidity in those patients [13]. Thandassery et al. reported a rare case in a patient who developed intramural duodenal hematoma after endoscopic retrograde cholangiopancreatogram (ERCP) with sphincterotomy and biliary stone extraction with subsequent of acute pancreatitis, biliary and gastric outlet obstruction after ERCP [12]. Our patient also had the triad of above symptoms. We also observed rapid decline of hemoglobin level in our patient and this observation has been described in other case reports [10, 14]. We suggest that the patients should be suspected to have IHD if they have the tetrad of acute pancreatitis, biliary obstruction, gastric outlet obstruction and rapid decline of hemoglobin after an endoscopic examination.

In uncomplicated cases, IDH usually resolves spontaneously with conservative treatment in 1–3 weeks [15]. Sadio et al. have reported a case in a patient with intramural gastric hematoma after endoscopic injection therapy, and have found that patient’s hematoma disappear six days later [14]. In our patient, the IDH was spontaneously resolved under abdominal sonography six days after the endoscopy.

To our best knowledge, less than 10 cases of patients with esophageal pneumatosis have been reported [4, 16], and no esophagogastroduodenal pneumatosis has been reported. The mechanism of PI has been experimentally proved that dissection of the gas from intraluminal to the intramural compartment is due to increased intra-abdominal pressure combined with mucosal defect [1]. We hypothesize that the findings of our patient are derived from the similar mechanism. The air was inflated from the defect of the needle injection site after endoscopic hemostasis for duodenal ulcer hemorrhage, and warfarin-associated coagulopathy precipitated the formation of IDH, which further dissected the duodenal wall, leading to inflated air entering into the duodenal, gastric and esophageal wall. The inflated air finally entered the portal vein through the portal circulation system.

Traditionally, once the pneumoporta is recognized along with PI, surgical intervention is preferred due to the concern of having ischemic bowel. But, PI is a radiological finding with wide spectrum of clinical severity and outcome. Surgical or conservative treatment should be considered according to the underlying etiology [1]. In this patient, esophagogastroduodenal pneumatosis and intramural duodenal hematoma were resolved spontaneously six days later. Therefore, we suggest that conservative treatment and close clinical assessment should be considered as an initial management for patients who complicate with IDH and PI after an endoscopic procedure. But, surgery is needed for those patients if the diseases progress or complications persist.