Moura Maria, Silva-Dos-Santos Amilcar, Afonso Joana, Talina Miguel
Unit of Child and Adolescent Psychiatry, Department of Psychiatry, Hospital Vila Franca de Xira, R. do Parque Res. dos Povos 1, 2600-009, Vila Franca de Xira, Portugal.
Department of Psychiatry, Hospital Vila Franca de Xira, R. do Parque Res. dos Povos 1, 2600-009, Vila Franca de Xira, Portugal.
BMC Res Notes. 2016 Jul 29;9:374. doi: 10.1186/s13104-016-2180-6.
Anti-NMDA receptor encephalitis is an autoimmune disease that was identified in 2007, and manifests in a stepwise manner with psychiatric, neurological and autonomic symptoms. The disease is caused by autoantibodies against NMDA receptors. It can have a paraneoplastic origin, mainly secondary to ovarian teratomas, but it can also be unrelated to the tumor. This disease can affect both sexes and all ages.
Here, we present a case of a 15 year-old female adolescent with first-episode psychosis with anti-NMDA receptor encephalitis not related to tumor, which manifested with delusion, hallucinations, panic attacks, agitation, and neurological symptoms, and later with autonomic instability. She was treated with immunotherapy and psychiatric medication resulting in improvement of her main psychiatric and neurological symptoms.
Our main objective in presenting this case is to alert clinicians to this challenging and recent disease that has a clinical presentation that might resemble a functional psychiatric condition and can be underdiagnosed in the context of child and adolescent psychiatry.
抗 N-甲基-D-天冬氨酸(NMDA)受体脑炎是一种 2007 年被确认的自身免疫性疾病,以精神、神经和自主神经症状逐步显现。该疾病由针对 NMDA 受体的自身抗体引起。它可能有副肿瘤性起源,主要继发于卵巢畸胎瘤,但也可能与肿瘤无关。这种疾病可影响各年龄段的男女。
在此,我们报告一例 15 岁女性青少年,患有与肿瘤无关的抗 NMDA 受体脑炎所致的首发精神病,表现为妄想、幻觉、惊恐发作、激越及神经症状,随后出现自主神经功能不稳定。她接受了免疫治疗和精神科药物治疗,主要的精神和神经症状得到改善。
我们呈现此病例的主要目的是提醒临床医生注意这种具有挑战性的新疾病,其临床表现可能类似于功能性精神疾病,在儿童和青少年精神病学背景下可能会被漏诊。