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Ovarian growing teratoma syndrome with multiple metastases in the abdominal cavity and liver: A case report

BACKGROUND: Growing teratoma syndrome (GTS) is an unusual presentation of an amazing transformation of teratoma from malignant to benign on pathology during or after systemic or intraperitoneal chemotherapy. The definitive pathogenesis is still not fully understood due to the lack of large-sample st...

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Autores principales: Hu, Xu, Jia, Zhong, Zhou, Li-Xin, Kakongoma, Nisile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125286/
https://www.ncbi.nlm.nih.gov/pubmed/35663054
http://dx.doi.org/10.12998/wjcc.v10.i14.4704
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author Hu, Xu
Jia, Zhong
Zhou, Li-Xin
Kakongoma, Nisile
author_facet Hu, Xu
Jia, Zhong
Zhou, Li-Xin
Kakongoma, Nisile
author_sort Hu, Xu
collection PubMed
description BACKGROUND: Growing teratoma syndrome (GTS) is an unusual presentation of an amazing transformation of teratoma from malignant to benign on pathology during or after systemic or intraperitoneal chemotherapy. The definitive pathogenesis is still not fully understood due to the lack of large-sample studies. CASE SUMMARY: A 53-year-old woman underwent radical surgery and postoperative intraperitoneal chemotherapy due to immature teratoma of the right ovary at the age of 28. She remained well during a 25-year follow-up period after surgery. Multiple asymptomatic solid masses were found in the liver on ultrasonography a month ago. Enhanced computed tomography (CT) of the abdomen revealed multiple masses in the abdominal cavity. The largest one was located in the posterior peritoneum next to the sixth segment of the right liver, about 7.9 cm × 7.5 cm in size. Three masses were present inside the liver, and one mass was in the right pelvic floor. Multiple lumps in the abdominal cavity were completely removed by surgery. During the operation, multiple space-occupying lesions were seen, ranging in size from 0.5 to 3 cm, and grayish white in color and hard in texture. Ovarian GTS was finally diagnosed based on postoperative pathology. After surgery, she recovered uneventfully. During a 3-year follow-up, the patient remained free of the disease without any recurrence on CT scan. CONCLUSION: GTS is a rare phenomenon characterized by conversion of immature teratoma to mature one during or after chemotherapy and presents as growing and metastasizing masses. The pathogenesis of GTS is unclear, and the prognosis is good after surgical resection.
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spelling pubmed-91252862022-06-04 Ovarian growing teratoma syndrome with multiple metastases in the abdominal cavity and liver: A case report Hu, Xu Jia, Zhong Zhou, Li-Xin Kakongoma, Nisile World J Clin Cases Case Report BACKGROUND: Growing teratoma syndrome (GTS) is an unusual presentation of an amazing transformation of teratoma from malignant to benign on pathology during or after systemic or intraperitoneal chemotherapy. The definitive pathogenesis is still not fully understood due to the lack of large-sample studies. CASE SUMMARY: A 53-year-old woman underwent radical surgery and postoperative intraperitoneal chemotherapy due to immature teratoma of the right ovary at the age of 28. She remained well during a 25-year follow-up period after surgery. Multiple asymptomatic solid masses were found in the liver on ultrasonography a month ago. Enhanced computed tomography (CT) of the abdomen revealed multiple masses in the abdominal cavity. The largest one was located in the posterior peritoneum next to the sixth segment of the right liver, about 7.9 cm × 7.5 cm in size. Three masses were present inside the liver, and one mass was in the right pelvic floor. Multiple lumps in the abdominal cavity were completely removed by surgery. During the operation, multiple space-occupying lesions were seen, ranging in size from 0.5 to 3 cm, and grayish white in color and hard in texture. Ovarian GTS was finally diagnosed based on postoperative pathology. After surgery, she recovered uneventfully. During a 3-year follow-up, the patient remained free of the disease without any recurrence on CT scan. CONCLUSION: GTS is a rare phenomenon characterized by conversion of immature teratoma to mature one during or after chemotherapy and presents as growing and metastasizing masses. The pathogenesis of GTS is unclear, and the prognosis is good after surgical resection. Baishideng Publishing Group Inc 2022-05-16 2022-05-16 /pmc/articles/PMC9125286/ /pubmed/35663054 http://dx.doi.org/10.12998/wjcc.v10.i14.4704 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Case Report
Hu, Xu
Jia, Zhong
Zhou, Li-Xin
Kakongoma, Nisile
Ovarian growing teratoma syndrome with multiple metastases in the abdominal cavity and liver: A case report
title Ovarian growing teratoma syndrome with multiple metastases in the abdominal cavity and liver: A case report
title_full Ovarian growing teratoma syndrome with multiple metastases in the abdominal cavity and liver: A case report
title_fullStr Ovarian growing teratoma syndrome with multiple metastases in the abdominal cavity and liver: A case report
title_full_unstemmed Ovarian growing teratoma syndrome with multiple metastases in the abdominal cavity and liver: A case report
title_short Ovarian growing teratoma syndrome with multiple metastases in the abdominal cavity and liver: A case report
title_sort ovarian growing teratoma syndrome with multiple metastases in the abdominal cavity and liver: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125286/
https://www.ncbi.nlm.nih.gov/pubmed/35663054
http://dx.doi.org/10.12998/wjcc.v10.i14.4704
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