Introduction: Acute esophageal necrosis (AEN), or black esophagus, is a rare condition that manifests as black mucosa of the distal esophagus with an abrupt transition at the gastroesophageal junction. AEN typically presents as an upper gastrointestinal bleed. Risk factors include male sex, advanced age, diabetes, coronary artery disease, pulmonary disease, gastroesophageal reflux, malignancy, and malnutrition in the setting of hemodynamic instability. Treatment includes management of underlying conditions, intravenous proton pump inhibitor therapy, nutrition, fluid resuscitation, and bowel rest. High mortality rates have been demonstrated but many patients can recover with supportive care. Case Description/Methods: A 67-year-old male with chronic obstructive pulmonary disease, peripheral vascular disease, and hypertension presented as a transfer for escalation of care of acute on chronic respiratory failure and triple vessel coronary artery disease. After 7 days of mechanical ventilation, the patient experienced oropharyngeal dysphagia and failed a swallow evaluation. Enteral access with dobhoff tube placement was attempted without success, prompting gastroenterology consult for endoscopic placement. He was tachycardic, normotensive, afebrile, and saturating well on 4 L nasal cannula. Labs showed a hemoglobin of 12 g/dL, blood urea nitrogen 12 mg/dL, and creatinine 0.64 mg/dL. He denied abdominal pain, vomiting, melena, or hematochezia. Endoscopy showed a normal upper third of the esophagus with distal black mucosa, and an abrupt transition at the gastroesophageal mucosa. Biopsy showed ulcer exudate and granulation tissue with acute inflammation, negative for CMV, HSV, or fungal organisms. Patient remained with nothing by mouth and on total parenteral nutrition. A do not resuscitate order was placed and the patient unfortunately expired from a ventricular arrythmia 4 days later (Figure). Discussion: This case demonstrates an unexpected finding of AEN in a patient presenting atypically with oropharyngeal dysphagia in the absence of obvious upper gastrointestinal bleeding. This patient's critical illness, age, and multiple medical comorbidities most likely contributed to his AEN. This case highlights the importance of maintaining a broad differential diagnosis for dysphagia in critically ill patients. It also highlights the need to evaluate the acute onset of dysphagia in this patient population prior to enteral tube placement, given high risk of perforation.[2456] Figure 1. A, C, D) black, necrotic appearing distal esophagus B) black, necrotic appearing distal esophagus with abrupt transition at the gastroesophageal junction.
Introduction: Dysphagia lusoria, also known as Bayford-Autenrieth dysphagia, is a rare condition with prevalence of approximately 0.5%. First reported by David Bayford in 1790, it is defined as dysphagia secondary to extrinsic compression of the esophagus as a result of congenital abnormality of the aortic arch and its branches. We report a case of Dysphagia lusoria in a patient with congenital heart syndrome. Case Description/Methods: A 36-year-old woman with history of Dysphagia lusoria secondary to an aberrant left subclavian artery (SCA), congenital heart syndrome with known right sided thoracic aorta, tricuspid atresia and stenosis, hypoplastic right ventricle, and aberrant left SCA presented to the hospital with worsening dysphagia. She reported vomiting with any solid foods and only tolerating pureed foods
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