Evidence map›Paper›PMID 42238946›Full record

ArticleGynecologic oncology reports2026

Single-port robotic resection of gliomatosis peritonei following immature ovarian teratoma in an adolescent: A case report.

Qingchi Zhang, Lingling Sun, Kuiran Dong

Abstract readCase Reports
In one paragraph

Article in Gynecologic oncology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Qingchi ZhangDepartment of Pediatric Surgery, Children's Hospital of Fudan University (Xiamen Branch), Xiamen Children's Hospital, Xiamen 361006, China.
Lingling SunDepartment of Pediatric Surgery, Children's Hospital of Fudan University (Xiamen Branch), Xiamen Children's Hospital, Xiamen 361006, China.
Kuiran DongDepartment of Pediatric Surgery, Children's Hospital of Fudan University, Shanghai 200032, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gliomatosis peritonei (GP) is a rare benign condition characterized by dissemination of mature glial tissue within the peritoneal cavity, most commonly associated with immature ovarian teratoma (IOT). Its radiological appearance may closely mimic malignant recurrence or growing teratoma syndrome, posing significant diagnostic and therapeutic challenges, particularly in pediatric and adolescent patients.Case:We report the case of a 12-year-old girl with a history of IOT who developed multiple peritoneal nodules after initial surgery and chemotherapy. Imaging findings raised concern for disease recurrence, while serum tumor markers remained within normal ranges. Single-port robotic-assisted surgical exploration and resection of all visible peritoneal lesions were performed. Histopathological examination confirmed mature astrocytic glial tissue with low proliferative activity, establishing the diagnosis of GP. The postoperative course was uneventful, with rapid recovery, minimal pain, and satisfactory wound healing. No recurrence was observed during 12 months of follow-up. Conclusion: This case highlights the importance of histopathological confirmation in distinguishing GP from malignant recurrence after IOT. Single-port robotic surgery may represent a feasible minimally invasive option for the management of multifocal GP in adolescents, offering precise resection with favorable postoperative recovery.

Indexed as

GliomatosisperitoneiImmature ovarianteratomaPediatricgynecologic oncologySingle-port robotic surgery

Identifiers

PMID42238946
PMCPMC13226124

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