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Concurrent NMDAR and GFAP Antibody Encephalitis During Pregnancy
Erkam Zengin1, Irina Kharisova2, Dokpe Emechebe3
1Neurology Department, SUNY Downstate Health Sciences University, Brooklyn, New York, USA erkam.zengin@downstate.edu.
This is the first case of concurrent anti-NMDAR and anti-GFAP antibody encephalitis in a pregnant woman with ovarian teratoma. Neurological recovery was significantly improved after delivery, underscoring timely diagnosis and management.
Area of Science:
- Neuroimmunology
- Neurology
Background:
- Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is a severe autoimmune neurological disorder often linked to ovarian teratomas, primarily affecting young women.
- Typical symptoms include altered consciousness, psychosis, movement disorders, seizures, and autonomic dysfunction, often requiring intensive care.
Observation:
- This case presents the first documented instance of concurrent NMDAR and anti-glial fibrillary acidic protein (GFAP) antibody encephalitis in a pregnant patient with an ovarian teratoma.
- The patient underwent teratoma removal and immunosuppressive therapy, but significant neurological improvement was observed only after childbirth.
Findings:
- The co-occurrence of NMDAR and GFAP antibody encephalitis in pregnancy poses unique diagnostic and therapeutic challenges.
- Postpartum neurological recovery suggests a potential influence of pregnancy-related factors on disease course and treatment response.
Implications:
- This case highlights the importance of considering concurrent autoimmune encephalitis in pregnant women, especially with teratoma.
- Early diagnosis, multidisciplinary management including teratoma removal and immunosuppression, and consideration of delivery timing are crucial for favorable outcomes in both mother and child.
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