国际妇产科学杂志 ›› 2019, Vol. 46 ›› Issue (3): 265-268.

• 病例报告 • 上一篇    下一篇

卵巢成熟性畸胎瘤合并腹膜胶质瘤病一例报告

胡超,朱诚程,占旖晴,鲁凯俊,张轶清   

  1. 241000安徽省芜湖市,皖南医学院附属弋矶山医院妇产科(胡超,朱诚程,张轶清);皖南医学院(占旖晴,鲁凯俊)
  • 收稿日期:2018-12-06 修回日期:2019-02-02 出版日期:2019-06-15 发布日期:2019-06-25
  • 通讯作者: 张轶清,E-mail:zhangyiqing5612@sina.com E-mail:zhangyiqing5621@sina.cn
  • 基金资助:
    皖南医学院中青年科研基金(WK2017F30)

A Case Report of Ovarian Mature Teratoma with Peritoneal Gliomatosis

HU Chao, ZHU Cheng-cheng, ZHAN Yi-qing, LU Kai-jun, ZHANG Yi-qing   

  1. Department of Obstetrics and Gynecology, Yijishan Hospital of Wannan Medical College, Wuhu 241001, Anhui Province, China (HU Chao, ZHU Cheng-cheng, ZHANG Yi-qing); Wannan Medical College, Wuhu 241000, Anhui Province, China (ZHAN Yi-qing, LU Kai-jun)
  • Received:2018-12-06 Revised:2019-02-02 Published:2019-06-15 Online:2019-06-25
  • Contact: ZHANG Yi-qing, E-mail:zhangyiqing5612@sina.com E-mail:zhangyiqing5621@sina.cn

摘要: 腹膜胶质瘤病(gliomatosis peritonei,GP)是一种罕见的疾病,迄今仅报道100余例,典型临床表现是良性的、成熟的胶质组织广泛分布于腹膜,常与卵巢未成熟畸胎瘤(ovarian immature teratoma,OIT)同时存在。临床上必须经过彻底的切片检查,确定为成熟神经胶质组织,方可确诊。治疗多与原发肿瘤相关,但因该病罕见,尚未建立一套标准治疗方案。另因有极少部分病例有恶变可能,需长期随访观察。近年来,对于GP在发病机制、治疗及随访等方面均有新的进展,故本文就GP的研究进展进行探讨,为后续治疗提供参考。

关键词: 病例报告, 腹膜肿瘤, 神经胶质瘤, 畸胎瘤, 卵巢肿瘤

Abstract: Gliomatosis peritonei(GP) is a rare disease. Up to now, only more than 100 cases have been reported. The typical clinical manifestations are benign and mature glial tissue widely distributed in the peritoneum, often coexisting with ovarian immature teratoma. Clinically, it is necessary to undergo a thorough biopsy to identify the mature glial tissue before the diagnosis can be confirmed. Treatment is mostly associated with primary tumors,but because of the rarity of the disease, a standard treatment scheme has not yet been established. In addition, because of the possibility of malignant transformation in a few cases, long-term follow-up is needed. In recent years, new progress has been made in the pathogenesis, treatment and follow-up of GP. Therefore, the research progress of GP is discussed in this paper to provide reference for subsequent treatment.

Key words: Case reports, Peritoneal neoplasms, Glioma, Teratoma, Ovarian neoplasms

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