S4717 The Deadly Leak: An Unusual Location of a Post-Repair Aortoesophageal Fistula

Introduction: Aortoesophageal fistula (AEF) is a rare, often fatal cause of upper gastrointestinal (GI) bleeding, typically resulting from thoracic aortic aneurysms, malignancy, foreign body ingestion, or prior aortic interventions. It classically presents with a herald bleed followed by catastrophic hemorrhage. While secondary AEFs typically occur near grafts, spontaneous fistulas in remote, non-grafted segments are rare. We present a case of spontaneous AEF 5 weeks after ascending aortic repair in a location remote from the graft. Case Description/Methods: A 64-year-old man with obesity and hypertension presented with chest pain and was diagnosed with an aortic dissection from the thoracic aorta to the iliac arteries. He underwent emergent ascending aortic repair with graft placement with eventual stable discharge. About 5 weeks later, he presented again with chest pain, dyspnea, and melena. Initial vitals were: temperature 97.6°F, BP 131/72 mmHg, pulse 54 bpm, RR 22, and SpO₂ 98% on room air. Hemoglobin was 7.2 g/dL, down from 9.8 at discharge. Computed tomography angiography (CTA) showed a new dissection flap distal to the left subclavian and descending to the left iliac artery with left renal infarction, consistent with a Type B aortic dissection. He was started on intravenous proton pump inhibitors, and melena temporarily resolved. On hospital day 5, he developed recurrent melena, hematemesis, and hemodynamic instability. Repeat CTA showed a 7 mm pseudoaneurysm of the descending thoracic aorta. Despite transfusions and supportive care, he suffered massive hematemesis and cardiac arrest. Emergent endoscopy revealed copious upper GI bleeding without a clear source. The procedure was aborted due to cardiovascular collapse, and the patient died. Autopsy confirmed a spontaneous AEF remote from the graft. Discussion: This case illustrates a rare AEF remote from the graft site in the setting of a Type B aortic dissection. Although prior aortic interventions, such as grafting, are known risk factors, this unusual fistula developed in the context of progressive aortic dissection without direct graft involvement, a rarely reported phenomenon. The rapid progression from herald bleed to exsanguination underscores the fatal nature of AEF and the need for high clinical suspicion in patients with aortic disease and GI bleeding, regardless of graft site.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001146328.49230.6c
Primary Topic
Infectious Aortic and Vascular Conditions
Type
article
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article

S4717 The Deadly Leak: An Unusual Location of a Post-Repair Aortoesophageal Fistula

Shahroz Fatima, Priya Kumari Maheshwari, Eman Kazi, Amita Malik et al.
The American Journal of Gastroenterology
Infectious Aortic and Vascular Conditions
article

S4717 The Deadly Leak: An Unusual Location of a Post-Repair Aortoesophageal Fistula

Shahroz Fatima, Priya Kumari Maheshwari, Eman Kazi, Amita Malik, Arlen Brickman, John Paul Nsubuga, Wang Li
article en

Abstract

Introduction: Aortoesophageal fistula (AEF) is a rare, often fatal cause of upper gastrointestinal (GI) bleeding, typically resulting from thoracic aortic aneurysms, malignancy, foreign body ingestion, or prior aortic interventions. It classically presents with a herald bleed followed by catastrophic hemorrhage. While secondary AEFs typically occur near grafts, spontaneous fistulas in remote, non-grafted segments are rare. We present a case of spontaneous AEF 5 weeks after ascending aortic repair in a location remote from the graft. Case Description/Methods: A 64-year-old man with obesity and hypertension presented with chest pain and was diagnosed with an aortic dissection from the thoracic aorta to the iliac arteries. He underwent emergent ascending aortic repair with graft placement with eventual stable discharge. About 5 weeks later, he presented again with chest pain, dyspnea, and melena. Initial vitals were: temperature 97.6°F, BP 131/72 mmHg, pulse 54 bpm, RR 22, and SpO₂ 98% on room air. Hemoglobin was 7.2 g/dL, down from 9.8 at discharge. Computed tomography angiography (CTA) showed a new dissection flap distal to the left subclavian and descending to the left iliac artery with left renal infarction, consistent with a Type B aortic dissection. He was started on intravenous proton pump inhibitors, and melena temporarily resolved. On hospital day 5, he developed recurrent melena, hematemesis, and hemodynamic instability. Repeat CTA showed a 7 mm pseudoaneurysm of the descending thoracic aorta. Despite transfusions and supportive care, he suffered massive hematemesis and cardiac arrest. Emergent endoscopy revealed copious upper GI bleeding without a clear source. The procedure was aborted due to cardiovascular collapse, and the patient died. Autopsy confirmed a spontaneous AEF remote from the graft. Discussion: This case illustrates a rare AEF remote from the graft site in the setting of a Type B aortic dissection. Although prior aortic interventions, such as grafting, are known risk factors, this unusual fistula developed in the context of progressive aortic dissection without direct graft involvement, a rarely reported phenomenon. The rapid progression from herald bleed to exsanguination underscores the fatal nature of AEF and the need for high clinical suspicion in patients with aortic disease and GI bleeding, regardless of graft site.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 41%
Infectious Aortic and Vascular Conditions
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