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鞍上生殖细胞瘤放化疗后透明隔内混合性生殖细胞肿瘤:新发异时性肿瘤还是复发性肿瘤?

Mixed germ cell tumors in septum pellucidum after radiochemotherapy of suprasellar germinoma: de novo metachronous or recurrent neoplasms?

作者信息

Eom Ki Seong, Kim Jong Moon, Kim Tae Young

机构信息

Department of Neurosurgery, Wonkwang University College of Medicine, 344-2 Shinyong-dong, Iksan, 570-711, South Korea.

出版信息

Childs Nerv Syst. 2008 Nov;24(11):1355-9. doi: 10.1007/s00381-008-0654-0. Epub 2008 Jun 17.

DOI:10.1007/s00381-008-0654-0
PMID:18560841
Abstract

INTRODUCTION

Mixed germ cell tumors (GCTs) consisting of a germinoma and a mature teratoma in the septum pellucidum have never been described previously; the patient we present here is the first reported example.

CASE REPORT

This case involves an 18-year-old man who presented with abnormal behavior, impairment in recent memory, and emotional change. Five years ago, he received five cycles of chemotherapy using cisplatin and ectoposide and 24G of local radiotherapy for clinical diagnosis of suprasellar germinoma in another hospital. The tumor was then completely resolute. Magnetic resonance imaging in our hospital revealed a large fatty mass located primarily in the septum pellucidum and some portions of the corpus callosum; a heterogeneous enhancing tumor was observed in the surrounding area. The second tumor was completely removed. The histological diagnosis was mixed GCTs containing the component of a germinoma and a mature teratoma.

CONCLUSION

This case is characterized by a second GCT occurring at a different site and with a different histological type, long after complete resolution of suprasellar germinoma. Although it is very difficult to draw conclusions about the correlation between the first and second GCTs, neurosurgeons should always pay attention to the pathological variety and dynamic pathological changes in GCTs once they start to examine and treat them.

摘要

引言

以前从未描述过由透明隔内的生殖细胞瘤和成熟畸胎瘤组成的混合性生殖细胞肿瘤(GCTs);我们在此介绍的患者是首例报告病例。

病例报告

该病例为一名18岁男性,表现为行为异常、近期记忆力减退和情绪变化。五年前,他在另一家医院接受了五个周期的顺铂和依托泊苷化疗以及24G的局部放疗,临床诊断为鞍上生殖细胞瘤。当时肿瘤完全消退。我院的磁共振成像显示一个主要位于透明隔和胼胝体部分区域的大脂肪肿块;在周围区域观察到一个不均匀强化的肿瘤。第二个肿瘤被完全切除。组织学诊断为包含生殖细胞瘤和成熟畸胎瘤成分的混合性GCTs。

结论

该病例的特点是在鞍上生殖细胞瘤完全消退很长时间后,在不同部位出现了第二种组织学类型不同的GCT。尽管很难就第一和第二种GCT之间的相关性得出结论,但神经外科医生一旦开始检查和治疗GCT,就应始终关注其病理多样性和动态病理变化。

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