Evidence map›Paper›PMID 39118721›Full record

ArticleAnnals of medicine and surgery (2012)2024

Immature ovarian teratoma with gliomatosis peritonei, paraneoplastic hyponatremia and growing teratoma syndrome: a case report and literature review.

Ana Rita Mira, Mark R Brincat, Shruti Zalawadia, Michail Sideris, James Dilley

Abstract readCase Reports
In one paragraph

Article in Annals of medicine and surgery (2012), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Ana Rita MiraDepartment of Gynaecological Oncology, Royal London Hospital, Barts Health NHS Trust, London.
Mark R BrincatDepartment of Gynaecological Oncology, Royal London Hospital, Barts Health NHS Trust, London.
Shruti ZalawadiaDepartment of Gynaecological Oncology, Royal London Hospital, Barts Health NHS Trust, London.
Michail SiderisDepartment of Gynaecological Oncology, Royal London Hospital, Barts Health NHS Trust, London.
James DilleyDepartment of Gynaecological Oncology, Royal London Hospital, Barts Health NHS Trust, London.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction and relevance: Paraneoplastic hyponatremia is often secondary to syndrome of inappropriate antidiuretic hormone secretion (SIADH) by tumour cells. Immature ovarian teratomas (IOT) are uncommon and may present with SIADH. Case report: A 26-year-old female presented with a 3-month history of abdominal pain and constipation. Imaging identified a mixed solid-cystic right ovarian mass containing fat and peritoneal deposits. Biochemistry showed severe, refractory hyponatremia (117 mmol/l). She underwent diagnostic fertility-preserving right salpingo-oophorectomy and resection of peritoneal nodules with the aim to achieve symptom control and hyponatraemia resolution. Pathology revealed a FIGO Stage 2 Grade 2 IOT with extensive benign peritoneal gliomatosis. Initial management was conservative. After 6 months of active follow-up, a rise in AFP, and recurrent hyponatremia supported the decision to administer three cycles of Bleomycin-Etoposide-Cisplatin chemotherapy. One month later, given radiological disease progression despite satisfactory biomarker response, cytoreductive surgery with complete macroscopic resection was performed. Pathology consisted solely of peritoneal mature glial elements: a growing teratoma syndrome (GTS). The patient remains disease-free after 2 years of surveillance. Clinical discussion: Specimen histological assessment from the patient's initial surgery showed immature neuroectodermal tubules, which are thought to be the source of vasopressin secretion. The authors hypothesise that recurrent hyponatremia and rising AFP levels represented postoperative disease relapse. Biochemical response despite radiological disease progression was pathognomonic of a GTS. Conclusion: Paraneoplastic SIADH secondary to an IOT must be considered in female patients presenting with abdominal symptoms and hyponatremia. Management requires a multidisciplinary approach. Serum electrolytes are useful surveillance biomarkers supplementary to tumour markers.

Indexed as

case reportgliomatosis peritoneigrowing teratoma syndromehyponatremiaimmature ovarian teratomasyndrome of inappropriate secretion of antidiuretic hormone (SIADH)

Identifiers

PMID39118721
PMCPMC11305768

What Socratic holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.