Joseph Konrad, van der Hock Sarah, Seth Ishith, Hapangama Nipuni, Gibson Lara, Cuomo Roberto, Rozen Warren M, Dhupar Nita
Department of Surgery, Port Macquarie Hospital, Port Macquarie, NSW, Australia.
Faculty of Science, Medicine, and Health, The University of Melbourne, Melbourne, VIC, Australia.
Arch Gynecol Obstet. 2025 Jun;311(6):1535-1541. doi: 10.1007/s00404-024-07779-6. Epub 2024 Nov 4.
Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is a potentially life-threatening autoimmune disorder which is strongly associated with ovarian teratomas in young female patients. The primary aim is to highlight the importance of considering NMDAR encephalitis in the differential diagnosis of young female patients presenting with acute or subacute neuropsychiatric symptoms, especially when accompanied by ovarian teratomas.
This case report and literature review detail the presentation, diagnosis, and treatment of a 35-year-old G4P3 Indigenous woman who initially presented with neuropsychiatric symptoms and fever, having a history of extensive drug and alcohol use. Misdiagnosed initially, the patient's lack of response to standard treatments led to further investigations, revealing paraneoplastic anti-NMDAR encephalitis secondary to a left ovarian teratoma. The report examines the treatment regimen followed, including prednisolone, intravenous immunoglobulin, rituximab injections, and laparoscopic bilateral salpingo-oophorectomy.
This case underscores the critical need for increased clinical vigilance for anti-NMDAR encephalitis in patients, particularly young females, presenting with neuropsychiatric symptoms and potential ovarian teratomas. The literature review accompanying the case report provides valuable insights into the presentation, diagnosis, and management of this complex condition. Lastly, this study emphasised the diagnostic challenges inherent in paraneoplastic neuropsychiatric syndromes, advocating for a multidisciplinary approach in similar clinical scenarios.
抗N-甲基-D-天冬氨酸受体(NMDAR)脑炎是一种潜在的危及生命的自身免疫性疾病,在年轻女性患者中与卵巢畸胎瘤密切相关。主要目的是强调在对出现急性或亚急性神经精神症状的年轻女性患者进行鉴别诊断时,尤其是伴有卵巢畸胎瘤时,考虑抗NMDAR脑炎的重要性。
本病例报告及文献综述详细介绍了一名35岁、孕4产3的原住民女性的临床表现、诊断及治疗过程。该患者最初表现为神经精神症状和发热,有大量吸毒和酗酒史。最初诊断错误,患者对标准治疗无反应促使进一步检查,结果显示继发于左侧卵巢畸胎瘤的副肿瘤性抗NMDAR脑炎。报告探讨了所采用的治疗方案, 包括泼尼松龙、静脉注射免疫球蛋白、利妥昔单抗注射以及腹腔镜双侧输卵管卵巢切除术。
本病例强调了临床对出现神经精神症状和潜在卵巢畸胎瘤的患者,尤其是年轻女性,提高抗NMDAR脑炎警惕性的迫切需求。病例报告所附的文献综述为这种复杂疾病的临床表现, 诊断及管理提供了宝贵的见解。最后,本研究强调了副肿瘤性神经精神综合征固有的诊断挑战,提倡在类似临床情况下采用多学科方法。