Anti-N-methyl-d-aspartate receptor encephalitis (NMDARE) is an autoimmune disorder with a clinical presentation that overlaps with that of a myriad of neuropsychiatric conditions. Delays in diagnosis have been linked to long-term complications that affect a patient's quality of life. A 60-year-old female patient with a medical history of emphysema with chronic respiratory failure, hypertension, diabetes, morbid obesity, and hyperlipidemia presented to the hospital after she was found confused at home with limited verbal output, raising concerns for cerebrovascular events or toxic metabolic encephalitis. Neuroimaging and EEG results were unremarkable. The patient continued to experience respiratory distress that delayed diagnostic procedures. She was later diagnosed with small-cell lung cancer, and cerebrospinal fluid tests were positive for anti-N-methyl-d-aspartate receptor antibodies. Gradual improvement in cognitive function and speech was noted after treatment with immunotherapy. This case study underscores the importance of considering rare neurological conditions in patients with heightened cardiovascular risk profiles. Furthermore, it provides insights into the potential diagnostic and therapeutic challenges that can arise in the domain of anti-NMDARE in such patients.
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http://dx.doi.org/10.7759/cureus.78702 | DOI Listing |
Brain
March 2025
School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Patients with anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis, often present with severe psychiatric symptoms, yet the neuropathological mechanisms underlying their cognitive deficits remain insufficiently understood. In this study, we constructed an animal model using anti-NMDAR IgG purified from the serum of patients with anti-NMDAR encephalitis, and we used IgG obtained from healthy individuals as a control. Daily administration of anti-NMDAR IgG into the medial prefrontal cortex (mPFC) of mice for 7 days resulted in cognitive impairments resembling clinical symptoms, which spontaneously resolved 30 days after discontinuing the injections.
View Article and Find Full Text PDFCureus
February 2025
Internal Medicine, St. Luke's University Health Network, Easton, USA.
Anti-N-methyl-d-aspartate receptor encephalitis (NMDARE) is an autoimmune disorder with a clinical presentation that overlaps with that of a myriad of neuropsychiatric conditions. Delays in diagnosis have been linked to long-term complications that affect a patient's quality of life. A 60-year-old female patient with a medical history of emphysema with chronic respiratory failure, hypertension, diabetes, morbid obesity, and hyperlipidemia presented to the hospital after she was found confused at home with limited verbal output, raising concerns for cerebrovascular events or toxic metabolic encephalitis.
View Article and Find Full Text PDFItal J Dermatol Venerol
March 2025
Unit of Dermatology Clinic, IRCCS San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy.
Cureus
February 2025
Internal Medicine, Centro Hospitalar Universitário de Lisboa Central, Lisbon, PRT.
Anti-N-methyl-D-aspartate (NMDA) receptor NMDAR) encephalitis is a relatively recent condition, classified as an immune-mediated disorder characterized by a complex neuropsychiatric syndrome and the presence of anti-GluN1 subunit antibodies against the NMDA receptor in cerebrospinal fluid (CSF). Although it is a rare disease, studies have identified it as one of the most common causes of autoimmune encephalitis. The pathophysiology of this condition is not yet fully understood, especially regarding its association with ovarian teratomas and other neoplasms.
View Article and Find Full Text PDFCureus
February 2025
Department of Internal Medicine, Monmouth Medical Center, Long Branch, USA.
Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis is a rare autoimmune disorder characterized by neuropsychiatric symptoms and the presence of immunoglobulin G (IgG) antibodies against the N-methyl-D-aspartate receptor 1 (NR1) subunit of NMDA receptors. It is often triggered by ovarian teratomas, especially in young women, and presents with a combination of psychiatric and neurological symptoms. Here, we present a case of a 25-year-old woman with a history of schizoaffective disorder and post-partum depression who presented with two months of bizarre behavior, agitation, and decreased sleep.
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