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腹膜胶质瘤病:生长性畸胎瘤综合征中具有特定结局的一种特殊实体。

Gliomatosis peritonei: a particular entity with specific outcomes within the growing teratoma syndrome.

作者信息

Bentivegna Enrica, Gonthier Clementine, Uzan Catherine, Genestie Catherine, Duvillard Pierre, Morice Philippe, Gouy Sebastien

机构信息

Departments of *Gynecologic Surgery, and †Pathology, and ‡UniversityParis Sud, Gustave Roussy Cancer Campus, Villejuif, France.

出版信息

Int J Gynecol Cancer. 2015 Feb;25(2):244-9. doi: 10.1097/IGC.0000000000000345.

Abstract

OBJECTIVES

Ovarian immature teratoma may be associated with peritoneal spread that could, after adjuvant chemotherapy, develop into disease exclusively composed of mature implants (growing teratoma syndrome) and/or gliomatosis peritonei (GP), defined as the presence of pure mature glial tissue. However, very few specific series are devoted to the outcomes of pure GP. This was the aim of the present study.

PATIENTS

From 1997 to 2013, data concerning patients treated for stage II/III immature teratoma were reviewed. All slides were reviewed by an expert pathologist. Patients with ovarian cancer associated with peritoneal spread in the form of pure GP (initially if patients were treated without adjuvant treatment or after adjuvant chemotherapy if done) were analyzed.

RESULTS

Ten patients fulfilled the inclusion criteria. The median age of patients at diagnosis was 36 years (range, 14-41 years). Six patients had undergone a conservative treatment. Five patients had macroscopic residual disease at the end of surgery.The median duration of follow-up from the diagnosis of GP was 39 months (range, 6-114 months). Six patients had undergone secondary surgery. Among them, 5 had incompletely resected macroscopic GP. No patients had died of their disease. All patients were asymptomatic at the time of the last consultation (1 of them with abnormal radiologic imaging).

CONCLUSIONS

Gliomatosis peritonei is a particular entity of the condition described as growing teratoma syndrome because residual peritoneal disease can be asymptomatic totally stable over a long period which raises the question of a more conservative surgical approach in patients with massive peritoneal spread.

摘要

目的

卵巢未成熟畸胎瘤可能伴有腹膜播散,在辅助化疗后,可能发展为仅由成熟种植灶组成的疾病(生长性畸胎瘤综合征)和/或腹膜胶质细胞瘤(GP),后者定义为存在纯成熟神经胶质组织。然而,专门针对纯GP结局的具体系列研究非常少。本研究旨在探讨此问题。

患者

回顾了1997年至2013年期间接受II/III期未成熟畸胎瘤治疗的患者数据。所有切片均由专业病理学家复查。分析了以纯GP形式出现腹膜播散的卵巢癌患者(如果患者未接受辅助治疗则为初始情况,若接受了辅助化疗则为化疗后情况)。

结果

10例患者符合纳入标准。诊断时患者的中位年龄为36岁(范围14 - 41岁)。6例患者接受了保守治疗。5例患者在手术结束时存在肉眼可见的残留病灶。从诊断为GP开始的中位随访时间为39个月(范围6 - 114个月)。6例患者接受了二次手术。其中5例患者的肉眼可见GP未完全切除。无患者死于该疾病。在最后一次会诊时所有患者均无症状(其中1例影像学检查异常)。

结论

腹膜胶质细胞瘤是生长性畸胎瘤综合征所描述病症的一种特殊类型,因为残留的腹膜疾病可能长期无症状且完全稳定,这就引发了对于腹膜广泛播散患者采用更保守手术方式的问题。

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