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小儿年龄组成熟松果体区畸胎瘤的管理

Management of mature pineal region teratomas in pediatric age group.

作者信息

Tanrıkulu Bahattin, Özek M Memet

机构信息

Acibadem University School of Medicine, Department of Neurosurgery, Division of Pediatric Neurosurgery, Istanbul, Turkey.

出版信息

Childs Nerv Syst. 2020 Jan;36(1):153-163. doi: 10.1007/s00381-019-04204-1. Epub 2019 May 29.

Abstract

PURPOSE

Mature pineal region teratomas differ from other pineal tumors in terms of their characteristic radiological appearance and their clinical outcome after gross total excision. Our aim is to share our clinical experience and treatment outcomes in pediatric patients with mature pineal region teratoma.

METHODS

In this retrospective study, we reviewed clinical, radiological, and surgical data of ten patients who had radiologically predicted diagnosis of pineal region teratoma and pathologically confirmed diagnosis of mature pineal region teratoma between years 2004 and 2017 in our clinic. Statistical analysis was performed with SPSS 20.

RESULTS

All patients were male. Ages of patients ranged between 5 and 17 (median age was 9.5). All of them presented with headache. Magnetic resonance imaging showed characteristic appearance of teratomas with variable degree of hydrocephalus. All patients had negative results for AFP and b-HCG levels. All patients had gross total resection of pineal tumor through occipital transtentorial approach with no permanent neurological deficit. Pathological results of all tumor samples were consistent with mature teratoma. None of them had adjuvant chemotherapy or radiotherapy. Follow-up periods ranged between 3 and 170 months (median follow-up period was 60.5 months). All patients are alive with no tumor recurrence.

CONCLUSIONS

Pediatric mature pineal region teratomas are benign tumors with characteristic MRI appearance and negative tumor markers. Their definitive treatment is gross total surgical excision. Occipital transtentorial approach is a safe procedure for treatment of pediatric mature pineal teratomas.

摘要

目的

成熟松果体区畸胎瘤在特征性影像学表现及全切除后的临床结局方面与其他松果体肿瘤不同。我们的目的是分享我们在小儿成熟松果体区畸胎瘤患者中的临床经验和治疗结果。

方法

在这项回顾性研究中,我们回顾了2004年至2017年期间在我们诊所接受治疗的10例患者的临床、影像学和手术数据,这些患者经影像学预测诊断为松果体区畸胎瘤,并经病理证实为成熟松果体区畸胎瘤。使用SPSS 20进行统计分析。

结果

所有患者均为男性。患者年龄在5至17岁之间(中位年龄为9.5岁)。他们均以头痛为首发症状。磁共振成像显示畸胎瘤具有特征性表现,并伴有不同程度的脑积水。所有患者的甲胎蛋白(AFP)和β-人绒毛膜促性腺激素(β-HCG)水平均为阴性。所有患者均通过枕下经小脑幕入路对松果体肿瘤进行了全切除,且无永久性神经功能缺损。所有肿瘤样本的病理结果均与成熟畸胎瘤一致。他们均未接受辅助化疗或放疗。随访时间为3至170个月(中位随访时间为60.5个月)。所有患者均存活,无肿瘤复发。

结论

小儿成熟松果体区畸胎瘤是具有特征性MRI表现和阴性肿瘤标志物的良性肿瘤。其确定性治疗方法是手术全切除。枕下经小脑幕入路是治疗小儿成熟松果体畸胎瘤的安全方法。

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