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

机译:与多焦骨骨骼参与的旋翼巨大甘蓝瘤在儿科女性患者中

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摘要

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,起源于神经嵴。肿瘤生长缓慢,无症状,但由于对邻近结构的压力,可引起症状。在头颈部,它们相对少见。我们在此报告一例罕见的多发性神经节神经瘤病例,该病例位于一名13岁女孩的咽旁间隙、髂骨和其他骨骼。患者接受了手术,切除了从咽旁间隙到颈部的巨大肿块,采用经腮腺和经宫颈联合入路。术后进行MIBG(碘-123-间碘苯胍)闪烁扫描,检测顶枕骨、腰椎、右髂翼内侧皮质和左肱骨受累情况。患者未接受任何辅助治疗。在接下来的12个月内,没有头颈部复发的证据。总之,如果可能的话,完全手术切除肿瘤是成功率高的治疗选择。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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