模仿脑膜瘤的原发性中枢神经系统神经母细胞瘤:病例报告

Journal of postgraduate medicine Pub Date : 2024-07-01 Epub Date: 2024-07-12 DOI:10.4103/jpgm.jpgm_58_24
K Yadav, P K Sharma, D K Singh, V K Mishra
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摘要

摘要:神经母细胞瘤是儿科最常见的颅外实体瘤(约占儿童肿瘤的8%-10%)。颅内神经母细胞瘤多数是由颅外原发部位转移而来,被称为继发性神经母细胞瘤。然而,原发性中枢神经系统神经母细胞瘤(PCN-NB)非常罕见,文献中仅有少数病例和系列病例报道。PCN-NB 主要是轴内病变,轴外受累主要是由于颅外原发部位转移累及颅骨所致。在此,我们报告了一例 23 岁女性患者的病例,她的右额叶区域有一个巨大的轴外占位性病变,该病变模仿脑膜瘤,令人惊讶的是,组织病理学结果提示为幕上神经母细胞瘤。患者接受了右额叶开颅手术,并进行了辛普森 1 级肿瘤切除术。切除的组织被送去进行组织病理学检查。位于轴外的 PCN-NB 极其罕见。由于放射成像不一致,术前诊断这些肿瘤变得非常困难,应将其作为轴外颅内占位性病变的鉴别诊断之一。组织病理学检查是诊断颅内神经母细胞瘤的关键。
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Primary central nervous system neuroblastoma mimicking a meningioma: A case report.

Abstract: Neuroblastomas are the most common extracranial solid tumor in the pediatric age group (~8%-10% of childhood neoplasms). Most cases of intracranial neuroblastomas occur due to metastasis from some primary extracranial sites and are known as secondary neuroblastomas. However, the occurrence of primary central nervous system neuroblastomas (PCN-NB) is very rare, and only a few cases and case series have been reported in the literature. PCN-NB is mainly an intra-axial pathology, and extra-axial involvement is mainly due to metastasis from some extracranial primary site with involvement of the skull bone. Herein we report a case of a 23-year-old female having a large extra-axial space-occupying lesion in the right frontal region that was mimicking a meningioma, and surprisingly the histopathology was suggestive of a supratentorial neuroblastoma. A right frontal craniotomy was made, and Simpson's grade 1 excision of the tumor was done. The excised tissue was sent for histopathological examination. PCN-NB located extra-axially are extremely rare to occur. Due to inconsistent radiological imaging, it becomes very difficult to diagnose these tumors preoperatively, and these should be kept in mind as one of the differential diagnoses of extra-axial intracranial space-occupying lesions. Histopathological examination is crucial in diagnosing the intracranial neuroblastomas.

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