Evidence map›Paper›PMID 42005808›Full record

ArticleGynecologic oncology reports2026

Surgical debulking with fertility preservation in primary extra-neural ependymoma presenting with widespread peritoneal and intra-abdominal disease: Case report and literature review.

Danielle Christmas, Harrison Odgers, Georgina Elton, Katrina Tang, Christine Kang, King Man Wan

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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2 · The registry

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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

6 authors.

Danielle ChristmasDepartment of Gynaecologic Oncology, Royal Hospital for Women, Barker Street, Randwick, NSW 2031, Australia.
Harrison OdgersDepartment of Gynaecologic Oncology, Royal Hospital for Women, Barker Street, Randwick, NSW 2031, Australia.
Georgina EltonDepartment of Gynaecologic Oncology, Royal Hospital for Women, Barker Street, Randwick, NSW 2031, Australia.
Katrina TangPrince of Wales Hospital, 320/346 Barker Street, Randwick, NSW 2031, Australia.
Christine KangPrince of Wales Hospital, 320/346 Barker Street, Randwick, NSW 2031, Australia.
King Man WanDepartment of Gynaecologic Oncology, Royal Hospital for Women, Barker Street, Randwick, NSW 2031, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Extra-neural ependymoma is an extremely rare neoplasm with reported cases arising from the ovary, pelvis, broad and uterosacral ligaments, peritoneum and mediastinum. Case Presentation: A 29-year-old woman presented with abdominal pain. Computed tomography demonstrated bilateral adnexal masses, omental and peritoneal nodules and a 140 mm left upper quadrant mass. FDG PET/CT showed avid, disseminated abdominal disease. CA125 was 265. Differential diagnoses included tubo-ovarian malignancy, peritoneal carcinomatosis, and mesenchymal tumours. Diagnostic laparoscopy with biopsy established Stage IV extra-neural ependymoma based on histological features, immunophenotype and the absence of central nervous system disease on magnetic resonance imaging. She underwent primary cytoreduction including en bloc hysterectomy with ultra-low anterior resection, right salpingoophorectomy, left salpingectomy, peritonectomy, splenectomy with en-bloc partial resection of the left hemi-diaphragm and loop ileostomy. Intraoperatively, the right ovary was utilised for ex-vivo in-vitro oocyte maturation, and the left ovary was conserved for oocyte retrieval and cryopreservation for future surrogacy. Adjuvant chemotherapy was recommended but declined. She remained well at eleven months post-operatively. Conclusion: Extra-neural ependymomas are exceedingly rare with five reported cases of peritoneal ependymoma. Extra-neural ependymomas demonstrate distinct histological and immunophenotypic profiles including increased architectural variability within the spindled cell perivascular pseudorosettes characteristic of ependymomas and diffuse ER and PR positivity. Given limited evidence, optimal management remains undefined however surgical cytoreduction continues to be the cornerstone of management across reported cases with adjuvant treatment individualised. Certain fertility preservation strategies are concurrently feasible within a multidisciplinary framework and should be considered given reported cases are predominantly seen in younger females.

Indexed as

EpendymomaExtra-axial ependymomaExtra-neural ependymomaFertility PreservationPerivascular pseudorosettes

Identifiers

PMID42005808
PMCPMC13083778

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