Lyle Megan R, Dolia Jaydevsinh N, Fratkin Jonathan, Nichols Todd A, Herrington Betty L
Department of Pediatrics, University of Mississippi Medical Center, Jackson, Mississippi, MS, USA.
Department of Medicine, University of Mississippi Medical Center, Jackson, Mississippi, MS, USA.
Child Neurol Open. 2015 Feb 16;2(1):2329048X14567531. doi: 10.1177/2329048X14567531. eCollection 2015 Jan-Mar.
Diffuse leptomeningeal glioneuronal tumor is unique for communicating hydrocephalus, diffuse leptomeningeal enhancement, cystic changes, absence of tumor cells in cerebral spinal fluid, and a cell population of both glial and neuronal copositivity. It has likely been misdiagnosed as mixed glioneuronal tumors, oligodendrogliomas, and neuroepithelial tumors. Children with signs of this tumor are often worked up for infection, rheumatologic disease, or disseminated primary malignancy, resulting in unnecessary testing and treatment. We describe a 14-year-old female with recurrent headaches, hydrocephalus, and diffuse leptomeningeal enhancement discovered to be neoplastic 1 year after initial presentation, owing to extensive and unrevealing infectious and immunologic workups. Biopsies revealed atypical cells with markers of both glial and neuronal cells, positivity for OLIG-2, and focal p53 positivity. Great response was seen with temozolomide and craniospinal irradiation. Additionally, we postulate additional diagnostic indicators that may aid in earlier diagnosis and treatment decisions.
弥漫性软脑膜胶质神经元肿瘤因交通性脑积水、弥漫性软脑膜强化、囊性改变、脑脊液中无肿瘤细胞以及同时存在胶质和神经元共阳性细胞群而独具特点。它很可能被误诊为混合性胶质神经元肿瘤、少突胶质细胞瘤和神经上皮肿瘤。有该肿瘤体征的儿童常被误诊为感染、风湿性疾病或播散性原发性恶性肿瘤,从而导致不必要的检查和治疗。我们描述了一名14岁女性,最初出现症状1年后,因广泛且无结果的感染和免疫检查,发现其患有复发性头痛、脑积水和弥漫性软脑膜强化,活检显示非典型细胞具有胶质和神经元细胞标志物、OLIG - 2阳性以及局灶性p53阳性。替莫唑胺和全脑脊髓放疗取得了很好的效果。此外,我们推测了可能有助于早期诊断和治疗决策的其他诊断指标。