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Parapharyngeal giant ganglioneuroma with multifocal bone involvement in a pediatric female patient

机译:小儿女性患者咽旁巨大神经节神经瘤多灶性骨受累

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Ganglioneuroma is a rare benign tumor that originates from neural crest. Tumor tends to be slow growing, asymptomatic but can cause symptoms because of pressure to neighboring structures. In the head and neck region they are relatively rarely seen. We hereby present a rare case of multiple ganglioneuromas that were located in parapharyngeal space, iliac bone and other bones in a 13-year-old girl. Patient underwent surgery for the excision of a large mass, extending from parapharyngeal space to neck, with transparotid and transcervical combined approach. After operation, MIBG (iodine-123-meta-iodobenzylguanidine) scintigraphy was performed and involvement of parietooccipital bone, lumbal vertebra, right iliac wing medial cortex and left humerus were detected. No adjuvant therapy was given to the patient. There is no evidence of recurrence in the head and neck region in the following 12 months. In conclusion, complete surgical excision of the tumor, if possible, is the treatment of choice with high success rate. Close clinical and radiological follow-up for these tumors after surgery should be made.
机译:神经节神经瘤是一种罕见的良性肿瘤,起源于神经c。肿瘤往往生长缓慢,无症状,但由于对邻近结构的压力会引起症状。在头部和颈部区域,它们很少见。在此,我们介绍了一个13岁女孩的咽旁间隙,骨和其他骨骼中多发神经节神经瘤的罕见病例。患者接受经腮腺和经颈联合手术切除大块肿物的手术,从咽旁间隙一直延伸到颈部。术后行MIBG(碘-123-间碘碘苄胍)闪烁显像,发现枕枕骨,腰椎,right翼内侧皮层和左侧肱骨受累。没有给予患者辅助治疗。在接下来的12个月中,没有头颈部复发的迹象。总之,如果可能的话,完全手术切除肿瘤是成功率高的首选治疗方法。手术后应对这些肿瘤进行密切的临床和放射学随访。

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