The patient, a 64-year-old woman, presented with a history of systemic lupus erythematosus characterized by antinuclear antibody and anti-double-stranded DNA positivity, chronic hypocomplementemia, polyarthritis, pericarditis, and lupus nephritis complicated by endstage renal disease. She had been receiving hemodialysis for ;3 years and peritoneal dialysis for many years prior to that. She also had a history of antiphospholipid syndrome (APS) characterized by persistently positive lupus anticoagulant, high-titer IgG and IgM anti-b 2glycoprotein I, and high-titer IgG and IgM anticardiolipin. She was receiving anticoagulation therapy for an episode of deep venous thrombosis complicated by pulmonary embolism. She was admitted for cachexia and found to have evidence suggestive of smoldering disseminated intravascular coagulation (DIC) (low fibrinogen and elevated D-dimer levels, prolonged prothrombin and partial thromboplastin times, low hemoglobin [Hgb] level, and low platelet count). While hospitalized, she developed coffee ground emesis, hypotension, and an acute drop in her Hgb concentration of 3 gm/dl. Upper gastrointestinal endoscopy revealed "black esophagus" involving the middle and lower portions of the esophagus (A and B) (lower third of the esophagus and gastroesophageal junction, respectively). Extensive thrombosis (arrows) and acute esophageal necrosis were confirmed by histopathologic examination (C and D [original magnification 3 10 and 3 20, respectively]). Acute esophageal necrosis appears black, circumferential, and can affect any portion of the esophagus. Risk factors include hypertension, diabetes, hyperlipidemia, and chronic kidney disease. Alcohol abuse, malnourishment, hypoalbuminemia, and history of vascular and thromboembolic disease are other risk factors. In this patient, a prothrombotic state due to APS and DIC likely contributed. Extensive evaluation did not reveal evidence of infection or malignancy. We suspect the DIC was due at least in part to APS. Evaluation of 8 cases suggests that acute esophageal necrosis is multifactorial in most patients (as in this patient) and has multiple risk factors for ischemic insult and decreased gastric mucosal defenses (1). Gastrointestinal ischemia involving the small bowel or colon has been reported in APS (2). To our knowledge, this is only the second reported case of acute esophageal necrosis in a patient with APS (3).