Stein-Wexler Rebecca, Wootton-Gorges Sandra L, Greco Claudia M, Brunberg James A
Department of Radiology, University of California, Davis Medical Center and U.C. Davis Children's Hospital, Sacramento, CA 95817, USA.
Pediatr Radiol. 2005 Jul;35(7):694-7. doi: 10.1007/s00247-005-1402-1. Epub 2005 Feb 19.
Paraneoplastic limbic encephalitis (PLE) is an unusual disorder that is characterized by the association of clinical limbic system abnormalities with neoplasia, usually malignancy. It has rarely been reported in children and then manifests during the teenage years. Diagnosis is often delayed, especially when the tumor has not been recognized. In adults, the diagnosis can be revealed by the presence of antineuronal antibodies. We describe an unusual case of behavioral disturbance leading rapidly to coma in a 14-year-old girl with CSF pleocytosis who was found 10 weeks later to have an immature ovarian teratoma. Although her symptoms eventually improved slightly after tumor excision, she died while in rehabilitation. PLE is an important diagnosis to consider in the teenage girl with symptoms of a progressive limbic disorder and CSF pleocytosis, and whose brain MR imaging demonstrates no abnormality or mild T2-weighted temporal lobe signal abnormality. When this constellation of findings presents in a teenage girl, the possibility of an underlying ovarian teratoma should be considered.
副肿瘤性边缘叶脑炎(PLE)是一种罕见的疾病,其特征是临床边缘系统异常与肿瘤形成相关,通常为恶性肿瘤。儿童病例鲜有报道,且多见于青少年时期。诊断往往延迟,尤其是在肿瘤未被识别时。在成人中,抗神经元抗体的存在可提示诊断。我们描述了一例不寻常的病例,一名14岁女孩出现行为障碍并迅速昏迷,脑脊液有细胞增多,10周后发现患有未成熟卵巢畸胎瘤。尽管肿瘤切除后她的症状最终略有改善,但仍在康复过程中死亡。对于有进行性边缘叶疾病症状和脑脊液细胞增多,且脑部磁共振成像无异常或T2加权像颞叶信号轻度异常的青少年女孩,PLE是一个需要考虑的重要诊断。当青少年女孩出现这一系列表现时,应考虑潜在卵巢畸胎瘤的可能性。