青少年恶性生殖细胞瘤的临床特征:北京一项多中心 10 年回顾性研究

Cancer Innovation Pub Date : 2023-08-20 DOI:10.1002/cai2.87
Qian Zhao, Miao Li, Qing Sun, Tian Zhi, Mei Jin, Wen Zhao, Xisi Wang, Chao Duan, Xiaoli Ma, Wanshui Wu, Weihong Zhao, Dongsheng Huang, Yan Su
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引用次数: 0

摘要

背景 本研究旨在回顾北京地区青少年恶性生殖细胞瘤(MGCTs)的临床特征,并分析该年龄组的特殊性。 方法 回顾性分析 34 例患者的临床特征、病理表现和生存结果。 结果 34 例患者中,女孩 12 例,男孩 22 例,颅外肿瘤 18 例(52.9%),其中睾丸肿瘤 1 例,卵巢肿瘤 5 例,骶尾部肿瘤 1 例,纵隔肿瘤 11 例。在组织学上,我们发现了未成熟畸胎瘤(6 例)、卵黄囊肿瘤(5 例)、混合恶性肿瘤(5 例)、胚胎癌(1 例)和精原细胞瘤(1 例)。三年无事件生存率(EFS)和总生存率(OS)分别为48.8%和62.9%。另有16例(47.1%)患者患有颅内肿瘤,其中9例位于松果体区,5例位于小脑上区,1例位于基底节,1例位于小脑。所有患者均有局部病变,疗效极佳,3 年 EFS 和 OS 分别为 93.7% 和 100%。 结论 青少年多发性神经胶质瘤非常罕见,与性别有很大关系,纵隔和松果体区是最常见的肿瘤部位。与其他青少年肿瘤和其他年龄组的间变性肿瘤相比,其预后良好。纵隔内的间变性肿瘤有与其他血液恶性肿瘤伴发的倾向,这些患者的预后极差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical characteristics of malignant germ cell tumors in adolescents: A multicenter 10-year retrospective study in Beijing

Clinical characteristics of malignant germ cell tumors in adolescents: A multicenter 10-year retrospective study in Beijing

Background

The aim of this study was to review clinical features of adolescent malignant germ cell tumors (MGCTs) in Beijing and analyze the peculiar characteristics of this age group.

Methods

Clinical characteristics, pathological presentations, and survival outcomes of 34 patients were analyzed retrospectively.

Results

Of 34 patients, 12 girls and 22 boys, 18 (52.9%) had an extra-cranial tumor, including one testicular tumor, five ovarian tumors, one sacrococcygeal tumor, and 11 mediastinal tumors. Histologically, we found immature teratomas (n = 6), yolk sac tumors (n = 5), mixed malignant tumors (n = 5), an embryonic carcinoma (n = 1), and seminoma (n = 1). Three-year event-free survival (EFS) and overall survival (OS) were 48.8% and 62.9%, respectively. Another 16 (47.1%) patients had an intracranial tumor, including nine in the pineal region, five in the suprasellar region, one in basal ganglia, and one in cerebellopontine. All patients had localized disease and an excellent outcome with 3-year EFS and OS of 93.7% and 100%, respectively.

Conclusions

Adolescent MGCTs are rare with a strong dependence on gender, and the mediastina and pineal region are the most common tumor locations. The prognosis is promising compared with that of other adolescent tumors and MGCTs in other age groups. MGCTs in mediastina have a tendency to companion with other hematological malignancies, and the prognosis is extremely poor in these patients.

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