目的：提高肾上腺节细胞神经瘤的诊断和治疗水平。
To elevate the diagnosis and treatment level of adrenal ganglioneuroblastoma.
目的：总结颈椎节细胞神经瘤的临床特点，探讨其手术治疗效果。
Objective: To investigate the clinical manifestation and surgical outcome of ganglioneuroma of cervical spine.
平滑肌瘤、平滑肌肉瘤、类癌、节细胞神经瘤也可以发生于胃肠道。
GISTs, leiomyomas, leiomyosarcomas, carcinoids, and ganglioneuromas occur within the GI tract.
方法：回顾分析18例经手术与病理证实为节细胞神经瘤的超声检查资料。
Methods: The clinical data of 18 cases (10 men and 8 women) with adrenal ganglioneuroma confirmed by surgical pathology were reviewed.
方法回顾性分析5例经手术病理证实肾上腺节细胞神经瘤的CT表现，并与手术病理作对照分析。
Methods CT findings of 5 patients with surgically and pathologically proved adrenal ganglioneuroma were retrospectively analyzed and compared with those of surgery and pathology.
结果皮质腺瘤12例，皮质腺癌5例，嗜铬细胞瘤3例，髓样脂肪瘤4例，转移瘤6例，肾上腺节细胞神经瘤1例。
Results Of 31 cases, there were 12 adenomas, 5 adenocarcinomas, 3 pheochromocytomas, 4 myelolipomas, 6 metastatic tumor and 1 adrenal ganglioneuroma.
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.
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.
目的探讨神经节细胞瘤的CT特征。
Objective To investigate CT characteristics of ganglioneuroma.
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.
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.
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