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已发表论文
卵巢未成熟畸胎瘤伴腹膜胶质瘤病及淋巴结胶质瘤病转移：一例报告
Authors Zhang J , Ji H, Sun M, Wang J, Liu P, Feng L, Zhang P, Gao J
Received 17 July 2025
Accepted for publication 16 November 2025
Published 8 December 2025 Volume 2025:17 Pages 5269—5275
DOI https://doi.org/10.2147/IJWH.S553268
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Matteo Frigerio
Jiaxin Zhang,1 Hongjing Ji,1 Meiyu Sun,2 Jiahui Wang,1 Peixuan Liu,1 Lu Feng,2 Pengxin Zhang,2 Jingchun Gao1
1Department of Obstetrics & Gynecology, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, 116011, People’s Republic of China; 2Department of Pathology, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, 116011, People’s Republic of China
Correspondence: Jingchun Gao, Department of Obstetrics and Gynecology, First Affiliated Hospital of Dalian Medical University, Zhongshan Road 222, Dalian, Liaoning, 116011, People’s Republic of China, Tel +86 411 83635963, Fax +86 411 83622844, Email jingchun_gao@hotmail.com
Abstract: Gliomatosis peritonei (GP) is a rare condition of mature glial tissue within the peritoneum. GP has been reported in approximately 100 cases worldwide, and it rarely occurs in young women or in patients with ovarian mature or immature teratomas during childhood. In patients with ovarian immature teratoma (OIT) combined with gliomatosis peritonei, the tumor is typically large and is often detected intraoperatively. Its neuroglial component may not only spread within the peritoneum but also metastasize via the lymphatic vessels. Pathologically confirmed lymph nodes containing mature neuroglial components and positive for glial fibrillary acidic protein (GFAP) are consistent with nodal gliomatosis (NG). In this report, we present a case of gliomatosis associated with OIT combined with GP, which involves lymph nodes.
Keywords: gliomatosis peritonei, ovarian immature teratoma, nodal gliomatosis, ovarian teratoma
1Department of Obstetrics & Gynecology, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, 116011, People’s Republic of China; 2Department of Pathology, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, 116011, People’s Republic of China
Correspondence: Jingchun Gao, Department of Obstetrics and Gynecology, First Affiliated Hospital of Dalian Medical University, Zhongshan Road 222, Dalian, Liaoning, 116011, People’s Republic of China, Tel +86 411 83635963, Fax +86 411 83622844, Email jingchun_gao@hotmail.com
Abstract: Gliomatosis peritonei (GP) is a rare condition of mature glial tissue within the peritoneum. GP has been reported in approximately 100 cases worldwide, and it rarely occurs in young women or in patients with ovarian mature or immature teratomas during childhood. In patients with ovarian immature teratoma (OIT) combined with gliomatosis peritonei, the tumor is typically large and is often detected intraoperatively. Its neuroglial component may not only spread within the peritoneum but also metastasize via the lymphatic vessels. Pathologically confirmed lymph nodes containing mature neuroglial components and positive for glial fibrillary acidic protein (GFAP) are consistent with nodal gliomatosis (NG). In this report, we present a case of gliomatosis associated with OIT combined with GP, which involves lymph nodes.
Keywords: gliomatosis peritonei, ovarian immature teratoma, nodal gliomatosis, ovarian teratoma