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多发性脑胶质瘤酷似中枢神经系统炎性脱髓鞘疾病:1例罕见病例并文献复习

Multiple cerebral gliomas mimicking central nervous system inflammatory demyelinating diseases: A rare case with review of literature.

作者信息

Xiong Yong-Jie, Zhao Xin-Ling, Wang Xiao-Yan, Pan Deng-Ji, Tian Dai-Shi

机构信息

Department of Neurology Department of Pathology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Medicine (Baltimore). 2017 Dec;96(52):e9456. doi: 10.1097/MD.0000000000009456.

Abstract

RATIONALE

Multiple cerebral gliomas (MCGs), usually classified into multifocal and multicentric subtypes, represent major diagnostic challenges as their clinical, radiologic, and pathohistological features are not uniform, often mimicking brain metastatic tumors or central nervous system inflammatory demyelinating diseases (IDD).

PATIENT CONCERNS

Here, we report a rare case of MCGs with isolated seizures and 4 lesions in the brain, that was initially misdiagnosed as IDD during treatment.

DIAGNOSIS

The pathological diagnosis was astrocytoma, which was classified as a World Health Organization grade II glioma.

INTERVENTIONS

The patient was treated with dexamethasone and sodium valproate when he was misdiagnosed as having IDD. After the pathological diagnosis was obtained, he was treated with temozolomide and radiotherapy.

OUTCOMES

Three months after the above treatment, the health of the patient had improved; he was asymptomatic, and presented with better radiological manifestations.

LESSONS

Diagnostic imaging is valuable in differential diagnosis. Magnetic resonance spectroscopy is a promising technique for the assessment and characterization of lesions, though its role in definitive diagnosis is not yet defined. Brain tissue biopsy remains the golden standard for definitive diagnosis. In China, for various reasons, craniotomy biopsy is not performed routinely in patients with multiple intracranial lesions, and stereotactic cranial biopsy may be a more viable option because of its safety and cost-effectiveness. In summary, this case demonstrates that MCGs need to be included in the differential diagnosis of unknown intracranial multiple lesions.

摘要

理论依据

多发性脑胶质瘤(MCGs)通常分为多灶性和多中心性亚型,由于其临床、放射学和病理组织学特征不统一,常酷似脑转移瘤或中枢神经系统炎性脱髓鞘疾病(IDD),因此是主要的诊断难题。

患者情况

在此,我们报告1例罕见的以孤立性癫痫发作为表现且脑内有4个病灶的MCGs病例,该病例在治疗初期被误诊为IDD。

诊断

病理诊断为星形细胞瘤,分类为世界卫生组织二级胶质瘤。

干预措施

该患者在被误诊为IDD时接受了地塞米松和丙戊酸钠治疗。获得病理诊断后,接受了替莫唑胺和放疗。

结果

上述治疗3个月后,患者健康状况改善;无症状,影像学表现更佳。

经验教训

诊断性影像学检查在鉴别诊断中具有重要价值。磁共振波谱是评估和表征病变的一种很有前景的技术,尽管其在明确诊断中的作用尚未明确。脑组织活检仍是明确诊断的金标准。在中国,由于各种原因,对于颅内多发病变患者不常规进行开颅活检,立体定向颅脑活检因其安全性和成本效益可能是更可行的选择。总之,该病例表明,MCGs需要纳入不明原因颅内多发病变的鉴别诊断中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853a/6392929/7327c684510d/medi-96-e9456-g002.jpg

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