Tekin Hande Gazeteci, Karaoğlu Pakize, Bolat Elif
Çiğli Regional Education Hospital, Pediatric Neurology Clinic, İzmir, Turkey.
Dr. Behçet Uz Children's Hospital, Pediatric Neurology Clinic, İzmir, Turkey.
Neurocirugia (Engl Ed). 2021 Feb 4. doi: 10.1016/j.neucir.2020.12.004.
Primary diffuse leptomeningeal oligodendrogliomatosis is a rare fatal tumor of childhood. Symptoms usually occur when the tumor causes hydrocephalus. Brain magnetic resonance imaging (MRI) may be nearly normal in the early stages of the disease, while hydrocephalus and multiple leptomeningeal cysts with spongiform appearance may appear later on. One may consider the diagnosis when radiologic findings become apparent with multiple leptomeningeal cysts. However, failure to recognize the imaging findings due to the rarity of the disease may delay the diagnosis. Here, we report a 3.5-year-old girl who presented with ataxia and vomiting and had a diagnosis of primary diffuse leptomeningeal glioneuronal tumor with remarkable brain MRI findings as diffuse multiple tiny cystic lesions on the brain and spinal cord. She benefited from radiotherapy and temozolomide treatment with remission of brain MRI findings. Increasing the number of reported cases will enable the elucidation of the disease's pathogenesis and the development of treatment protocols.
原发性弥漫性软脑膜少突胶质细胞瘤是一种罕见的儿童致命肿瘤。症状通常在肿瘤导致脑积水时出现。在疾病早期,脑磁共振成像(MRI)可能近乎正常,而脑积水和多个具有海绵状外观的软脑膜囊肿可能在后期出现。当影像学检查发现多个软脑膜囊肿时,可考虑诊断。然而,由于该疾病罕见而未能识别影像学表现可能会延迟诊断。在此,我们报告一名3.5岁女孩,她出现共济失调和呕吐,诊断为原发性弥漫性软脑膜神经胶质瘤,脑部MRI表现显著,为脑和脊髓弥漫性多发微小囊性病变。她接受放疗和替莫唑胺治疗后脑部MRI表现缓解。增加报告病例数将有助于阐明该疾病的发病机制并制定治疗方案。