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A unique uterine cervical “teratocarcinosarcoma”: a case report

BACKGROUND: Teratocarcinosarcoma (TCS) is a rare aggressive tumor of the nasal cavity and paranasal sinuses and has both epithelial and two or more mesenchymal components. In other organs, 5 cases of ovarian tumors closely resembling TCS have been reported; however, there has been no published case...

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Autores principales: Ito, Kozue, Yano, Mitsutake, Ogasawara, Aiko, Miwa, Maiko, Kozawa, Eito, Yasuda, Masanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827231/
https://www.ncbi.nlm.nih.gov/pubmed/31684979
http://dx.doi.org/10.1186/s13000-019-0890-5
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author Ito, Kozue
Yano, Mitsutake
Ogasawara, Aiko
Miwa, Maiko
Kozawa, Eito
Yasuda, Masanori
author_facet Ito, Kozue
Yano, Mitsutake
Ogasawara, Aiko
Miwa, Maiko
Kozawa, Eito
Yasuda, Masanori
author_sort Ito, Kozue
collection PubMed
description BACKGROUND: Teratocarcinosarcoma (TCS) is a rare aggressive tumor of the nasal cavity and paranasal sinuses and has both epithelial and two or more mesenchymal components. In other organs, 5 cases of ovarian tumors closely resembling TCS have been reported; however, there has been no published case of cervical TCS. Herein, we describe a unique case of cervical tumor that had carcinosarcomatous and teratomatous features, resembling a sinonasal TCS. CASE PRESENTATION: A 45-year-old woman presented to our hospital for evaluation of a cervical lesion. The gynecologist found a large polypoid mass, whose biopsy showed glandular components of probable germ cell origin based on the immunohistochemical features. The patient underwent total hysterectomy with bilateral salpingo-oophorectomy. The cervical polypoid mass was found to consist of both epithelial and mesenchymal tissues, including immature glandular structure resembling fetal enteric tubules, neuroepithelial cells, hyaline cartilage, and rhabdomyosarcoma cells. This tumor was diagnosed as TCS of the uterine cervix. Following the surgery, the patient received radiotherapy and has been free of disease for 13 months. CONCLUSION: This is the first case report of cervical TCS. The tumor is thought to be histogenetically less associated with HPV infection, and its teratomatous components with an absence of cytogenetic abnormalities (including isochromosome 12p (i(12p)) suggest a analogous histogenesis compared to pure mature or immature teratoma.
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spelling pubmed-68272312019-11-07 A unique uterine cervical “teratocarcinosarcoma”: a case report Ito, Kozue Yano, Mitsutake Ogasawara, Aiko Miwa, Maiko Kozawa, Eito Yasuda, Masanori Diagn Pathol Case Report BACKGROUND: Teratocarcinosarcoma (TCS) is a rare aggressive tumor of the nasal cavity and paranasal sinuses and has both epithelial and two or more mesenchymal components. In other organs, 5 cases of ovarian tumors closely resembling TCS have been reported; however, there has been no published case of cervical TCS. Herein, we describe a unique case of cervical tumor that had carcinosarcomatous and teratomatous features, resembling a sinonasal TCS. CASE PRESENTATION: A 45-year-old woman presented to our hospital for evaluation of a cervical lesion. The gynecologist found a large polypoid mass, whose biopsy showed glandular components of probable germ cell origin based on the immunohistochemical features. The patient underwent total hysterectomy with bilateral salpingo-oophorectomy. The cervical polypoid mass was found to consist of both epithelial and mesenchymal tissues, including immature glandular structure resembling fetal enteric tubules, neuroepithelial cells, hyaline cartilage, and rhabdomyosarcoma cells. This tumor was diagnosed as TCS of the uterine cervix. Following the surgery, the patient received radiotherapy and has been free of disease for 13 months. CONCLUSION: This is the first case report of cervical TCS. The tumor is thought to be histogenetically less associated with HPV infection, and its teratomatous components with an absence of cytogenetic abnormalities (including isochromosome 12p (i(12p)) suggest a analogous histogenesis compared to pure mature or immature teratoma. BioMed Central 2019-11-04 /pmc/articles/PMC6827231/ /pubmed/31684979 http://dx.doi.org/10.1186/s13000-019-0890-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Ito, Kozue
Yano, Mitsutake
Ogasawara, Aiko
Miwa, Maiko
Kozawa, Eito
Yasuda, Masanori
A unique uterine cervical “teratocarcinosarcoma”: a case report
title A unique uterine cervical “teratocarcinosarcoma”: a case report
title_full A unique uterine cervical “teratocarcinosarcoma”: a case report
title_fullStr A unique uterine cervical “teratocarcinosarcoma”: a case report
title_full_unstemmed A unique uterine cervical “teratocarcinosarcoma”: a case report
title_short A unique uterine cervical “teratocarcinosarcoma”: a case report
title_sort unique uterine cervical “teratocarcinosarcoma”: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6827231/
https://www.ncbi.nlm.nih.gov/pubmed/31684979
http://dx.doi.org/10.1186/s13000-019-0890-5
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