NA NA NA A 20-year-old male with no known past medical history presented with two months of episodic right-sided weakness. An extensive workup was notable for a lumbar puncture that was positive for antibodies to the N-methyl-D-aspartate (NMDA) receptor, confirming anti-NMDA receptor (NMDAR) encephalitis. Baseline cardiac workup included a transthoracic echocardiogram (TTE) that showed left ventricular (LV) hypokinesis with borderline ejection fraction (EF 52%), and an ECG showing sinus tachycardia (Figure-A). While admitted, the patient developed shock, necessitating intubation and vasopressors. Serial ECGs while in shock showed sinus tachycardia, a prolonged QTc, and broad sail-like T wave in V1 (similar to type 1 Brugada pattern), with ST elevations in aVR and diffuse ST depressions inferolaterally (Figure-B). Serial troponins were minimally elevated (0.11 ug/L) and TTE showed no regional wall motion abnormalities, so invasive coronary angiography was not pursued. During progressive shock, the patient developed a wide complex tachycardia (WCT, Figure-C), that was thought to most likely be LV outflow tract ventricular tachycardia. The patient became hemodynamically unstable with the WCT, necessitating amiodarone, lidocaine, and ultimately five cardioversions. Repeat TTE showed severe biventricular dysfunction, and the patient needed veno-arterial extracorporeal membrane oxygenation (VA-ECMO). Ultimately, the patient’s biventricular function recovered, and he was able to be decannulated from VA-ECMO. He was managed with intravenous immunoglobulin, steroids and rituximab for his anti-NMDAR encephalitis. Cardiac arrhythmias are a known complication of anti-NMDAR encephalitis in up to one-third of patients. To the best of our knowledge, this is the first case of anti-NDMAR encephalitis associated with diffuse ST elevations suggestive of ischemia. Models suggest NMDA receptor-mediated signaling in the nervous system can alter the vagal outflow to the heart, leading to sinus brady/tachycardia. Other explanations for ECG changes in our patient include focal myocarditis/vasospasm. This is an unusual case of marked ST elevation and sustained VT in anti-NMDAR encephalitis. Pathogenesis and management of arrhythmias related to this condition warrant further study.
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