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

Author:

Mira Ana Rita12,Brincat Mark R.1,Zalawadia Shruti1,Sideris Michail13,Dilley James14

Affiliation:

1. Department of Gynaecological Oncology, Royal London Hospital, Barts Health NHS Trust, London

2. Department of Gynaecology and Obstetrics, Hospital Garcia de Orta, Almada, Portugal

3. Wolfson Institute of Population Health, Barts CRUK Cancer Centre

4. Barts Cancer Institute, Queen Mary University of London, London, UK

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference16 articles.

1. Gliomatosis peritonei: a clinicopathologic and immunohistochemical study of 21 cases;Liang;Mod Pathol,2015

2. Immature teratoma: a case report of a monster tumour in the pediatric age group;Patel;Cureus,2023

3. Gliomatosis peritonei with malignant transformation: a case report and review of the literature;Shefren;Am J Obstet Gynecol,1991

4. Gliomatosis peritonei with malignant transformation;Dadmanesh;Mod Pathol,1997

5. Syndrome of inappropriate antidiuretic hormone secretion associated with an ovarian immature teratoma: a case report and review of the literature;Hom-Tedla;Gynecol Oncol Rep,2022

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3