Ma Lichao, Meng GuoLu, Tang Jie, Hou Yuanzheng
Department of Endocrinology, Second Medical Center, Chinese People's Liberation Army General Hospital, National Clinical Research Center for Geriatric Diseases, Beijing, China.
Department of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, China.
J Neurosurg Case Lessons. 2024 Dec 23;8(26). doi: 10.3171/CASE24701.
Diffuse leptomeningeal glioneuronal tumor (DLGNT) is a rare central nervous system tumor, especially in adult females. Typically, it presents with leptomeningeal enhancements in the basal cisterns and spinal cord. However, varied radiological and pathological features can complicate the diagnosis, as the present case illustrates.
An adult female presented with severe headache, blurred vision, and cognitive impairment. Elevated intracranial pressure (ICP) was detected via lumbar puncture. Brain magnetic resonance imaging (MRI) revealed atypical unilateral basal cistern enhancement, differing from the usual symmetrical DLGNT presentation. Despite high ICP, only mild ventricular enlargement was observed. Noncontrast spine MRI failed to demonstrate spinal leptomeningeal enhancement. A stereotactic biopsy of an occipital lesion was inconclusive. These atypical findings led to misdiagnoses of viral encephalitis or inflammation at two hospitals. Significant symptom relief occurred only after ventriculoperitoneal (VP) shunt surgery. Over 2.5 years, intraparenchymal lesions in the parahippocampal gyrus grew, necessitating surgical intervention. Pathological examination finally confirmed DLGNT. Postsurgery, the patient underwent chemotherapy with temozolomide and remains symptom free.
This case underscores the critical importance of comprehensive initial imaging, strategic biopsy planning, and timely placement of a VP shunt in patients with DLGNT. It contributes to the literature by revealing atypical imaging features and long-term progression patterns of DLGNT. https://thejns.org/doi/10.3171/CASE24701.
弥漫性软脑膜神经胶质瘤(DLGNT)是一种罕见的中枢神经系统肿瘤,在成年女性中尤为少见。通常,它表现为脑基底池和脊髓的软脑膜强化。然而,正如本病例所示,各种不同的放射学和病理学特征会使诊断变得复杂。
一名成年女性出现严重头痛、视力模糊和认知障碍。通过腰椎穿刺检测到颅内压(ICP)升高。脑部磁共振成像(MRI)显示非典型的单侧脑基底池强化,与常见的对称性DLGNT表现不同。尽管颅内压升高,但仅观察到轻度脑室扩大。非增强脊柱MRI未显示脊髓软脑膜强化。对枕部病变进行立体定向活检结果不明确。这些非典型表现导致在两家医院被误诊为病毒性脑炎或炎症。仅在进行脑室腹腔(VP)分流手术后症状才得到明显缓解。在超过2.5年的时间里,海马旁回的脑实质内病变不断增大,需要进行手术干预。病理检查最终确诊为DLGNT。术后,患者接受了替莫唑胺化疗,目前无症状。
本病例强调了全面的初始影像学检查、合理的活检规划以及及时为DLGNT患者放置VP分流管的至关重要性。它通过揭示DLGNT的非典型影像学特征和长期进展模式为文献做出了贡献。https://thejns.org/doi/10.3171/CASE24701