病理学诊断副神经节瘤。
大部分副神经节瘤的首选治疗方式是外科手术切除。
The treatment of choice is often surgical resection for most paragangliomas.
基于对免疫染色类型的描述，此肿瘤可能是副神经节瘤。
Based on description of immunohistochemical staining pattern, this tumor should probably be classified as paraganglioma.
无机能性腺瘤与神经节瘤相似表现为肿块较大，密度略低；
Similar to ganglioma, non-functional adenoma was large and slightly low in density.
颈静脉孔区肿块的鉴别诊断包括：副神经节瘤、脑膜瘤、淋巴瘤或转移瘤。
Differential considerations for a jugular foramen mass include: paraganglioma, meningiomas, lymphoma, or metastatic disease.
目的：分析不同部位副神经节瘤的CT表现及其病理特点，评价其临床诊断价值。
Objective: To investigate pathologic characteristics and the value of ct in diagnosing paraganglioma.
头颈部副神经节瘤是一罕见偶发的疾病，盛行率约占所有头颈部肿瘤的三万分之一。
Paragangliomas of head and neck are rare tumors that occur sporadically with the prevalence of about1 in30,000 of head and neck tumors.
结论：散发性副神经节瘤患者中存在SDHB基因突变，可能与副神经节瘤的发生有关。
CONCLUSIONS: The mutation of SDHB exists in sporadic paragangliomas patients and it might play a significant role in paragangliomas tumorigenesis.
结论：本文报道了一罕见的恶性的神经节瘤病例并讨论了针对远处转移灶可用的辅助治疗如i131 - MIBG传统放疗，化疗等。
Conclusion. We report a rare case of malignant paraganglioma and discussed adjuvant treatments to consider for distant metastases, such as I131-MIBG, conventional radiotherapy, and chemotherapy.
目的：本文旨在讨论脊柱神经节瘤的临床表现及治疗。神经节瘤起源于交感神经节的神经嵴细胞，为一少见的肾上腺外的副神经节肿瘤。
Objective. To discuss the spinal presentation and treatment of paraganglioma, a rare tumor of the extra-adrenal paraganglia, derived from neural crest cells in sympathetic ganglions.
目的研究小儿纵隔及腹膜后神经节细胞瘤的CT表现。
Objective To study the CT appearances of mediastinal and retroperitoneal ganglioneuroma in children.
嗜铬细胞瘤和副神经节细胞瘤中大约有10%属于遗传性疾病。
About 10% of the pheochromocytomas and paragangliomas belong to inherited causes.
目的探讨神经节细胞瘤的CT特征。
Objective To investigate CT characteristics of ganglioneuroma.
结论颈静脉球瘤是一种起源于副神经节的少见肿瘤，呈侵袭性生长，有低度恶性的生物学行为。
Conclusions Glomus jugulare tumor is a rare neoplasm arising from the paraganglion and it purses an aggressive ability and lower grade biological behavior.
神经节苷脂gm3作为一种促分化剂已在多个细胞瘤株模型中得到证实，但迄今为止其促分化的详细机制仍未阐明。
Ganglioside GM3 has been proved to be a physiological cell differentiation inducer in several human leukemia cell lines. However, the inducing differentiation mechanism of GM3 remains unclear.
典型的神经节神经胶质瘤表现为一个囊性肿块，接近40%的确诊病例可以见到一个壁结节。
Classically, ganglioglioma is described as a cystic mass with a mural nodule in approximately 40% of diagnosed cases.
方法：应用高效薄层色谱法对32例RB瘤组织及2 1例对照视网膜组织的神经节苷脂进行对照分析。
Methods: The gangliosides extracted from 32 samples of tumor tissues of RB and 21 control retina tissues were analyzed with high performance thin layer chromatography.
方法：应用高效薄层色谱法对32例RB瘤组织及2 1例对照视网膜组织的神经节苷脂进行对照分析。
Methods: The gangliosides extracted from 32 samples of tumor tissues of RB and 21 control retina tissues were analyzed with high performance thin layer chromatography.
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