Krunal H. Patel¹, Yuvraj Chowdhury², Mrinali Shetty³, Vaibhavi Uppin², Paul Madaj², Moro O. Salifu¹, Mary Youssef¹, Victoria L. Henglein¹, Samy I. McFaralne^1,

Described in 2007, anti-N-methyl-d-aspartate receptor encephalitis (ANMDARE) is a rare autoimmune limbic encephalitis affecting young adults (predominantly women of reproductive age) and is a paraneoplastic manifestation of ovarian teratoma in about half of the cases. ANMDARE is characterized by psychiatric changes, neurological changes, autonomic instability and cardiac dysrhythmias. In this report, we present a 36-year-old woman who was 16 weeks pregnant and brought to the hospital with confusion and subsequently had a seizure with Electroencephalography (EEG) demonstrated an extreme delta brush pattern consistent with ANMDARE. Patient developed sinus nodal dysfunction and was also found to have ovarian teratoma, a rather typical presentation for ANMDARE, that is considered a paraneoplastic syndrome for ovarian teratoma. In this report, we highlight the cardiac manifestation of ANMDARE, the pathophysiology associated with autonomic instability, and management strategies of this rare, and largely devastating illness.

anti-N-methyl-d-aspartate receptor encephalitis (ANMDARE), Lock Step Phenomenon, autoimmune encephalitis, ovarian teratoma, autonomic dysregulation, sinus node dysfunction