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Synchronous uterine adenocarcinoma and leiomyosarcoma – a case study

Synchronous gynecological cancers are rarely described. Those cases account for approximately up to 6% of female genital tract malignancies. The presence of synchronous endometrial adenocarcinoma and gynecological tract neoplasia is rare – the most commonly described is synchronous adenocarcinoma an...

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Autores principales: Dudzik, Kamila, Krzysteczko, Agnieszka, Kolny, Leon, Bąk, Agnieszka, Stawicka-Ociepka, Ewelina, Nowosielski, Krzysztof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437056/
https://www.ncbi.nlm.nih.gov/pubmed/28546804
http://dx.doi.org/10.5114/pm.2017.67367
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author Dudzik, Kamila
Krzysteczko, Agnieszka
Kolny, Leon
Bąk, Agnieszka
Stawicka-Ociepka, Ewelina
Nowosielski, Krzysztof
author_facet Dudzik, Kamila
Krzysteczko, Agnieszka
Kolny, Leon
Bąk, Agnieszka
Stawicka-Ociepka, Ewelina
Nowosielski, Krzysztof
author_sort Dudzik, Kamila
collection PubMed
description Synchronous gynecological cancers are rarely described. Those cases account for approximately up to 6% of female genital tract malignancies. The presence of synchronous endometrial adenocarcinoma and gynecological tract neoplasia is rare – the most commonly described is synchronous adenocarcinoma and endometrial ovarian cancer (accounting for 15-20% of ovarian neoplasia and 5% of endometrial cancers). Concomitant uterine carcinosarcoma and ovarian cancer, or endometrial adenocarcinoma are extremely rare. Up till now, only 3 cases of synchronous adenocarcinoma and leiomyosarcoma were described. In the present study a case of 60-year-old woman diagnosed with synchronous endometrial adenocarcinoma and leiomyosarcoma uteri is described. As the preoperative evaluation revealed endometrial adenocarcinoma G2 with intermediate-risk of lymph node metastasis and synchronous leiomyosarcoma G3, total hysterectomy with bilateral salpingo-oophorectomy and systemic lymphadenectomy was performed showing no lymphatic involvement. In the postoperative evaluation the patient was qualified to adenocarcinoma low recurrence-risk group (adenocarcinoma G1 with no LVSI, FIGO IA) – no further radiotherapy was required. However, as synchronous leiomyosarcoma G3 was diagnosed, we decided to refer the patient for adjuvant chemotherapy. Contemporary recommendation on the diagnosis and treatment of uterine carcinomas, especially uterine leiomyosarcomas, is also described in this paper. The presented case showed that diagnosis and treatment of women with uterine tumors should be individualized as in the same case an extremely rare cancer type can be present which, consequently, changes the treatment regimen and prognosis.
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spelling pubmed-54370562017-05-25 Synchronous uterine adenocarcinoma and leiomyosarcoma – a case study Dudzik, Kamila Krzysteczko, Agnieszka Kolny, Leon Bąk, Agnieszka Stawicka-Ociepka, Ewelina Nowosielski, Krzysztof Prz Menopauzalny Case Report Synchronous gynecological cancers are rarely described. Those cases account for approximately up to 6% of female genital tract malignancies. The presence of synchronous endometrial adenocarcinoma and gynecological tract neoplasia is rare – the most commonly described is synchronous adenocarcinoma and endometrial ovarian cancer (accounting for 15-20% of ovarian neoplasia and 5% of endometrial cancers). Concomitant uterine carcinosarcoma and ovarian cancer, or endometrial adenocarcinoma are extremely rare. Up till now, only 3 cases of synchronous adenocarcinoma and leiomyosarcoma were described. In the present study a case of 60-year-old woman diagnosed with synchronous endometrial adenocarcinoma and leiomyosarcoma uteri is described. As the preoperative evaluation revealed endometrial adenocarcinoma G2 with intermediate-risk of lymph node metastasis and synchronous leiomyosarcoma G3, total hysterectomy with bilateral salpingo-oophorectomy and systemic lymphadenectomy was performed showing no lymphatic involvement. In the postoperative evaluation the patient was qualified to adenocarcinoma low recurrence-risk group (adenocarcinoma G1 with no LVSI, FIGO IA) – no further radiotherapy was required. However, as synchronous leiomyosarcoma G3 was diagnosed, we decided to refer the patient for adjuvant chemotherapy. Contemporary recommendation on the diagnosis and treatment of uterine carcinomas, especially uterine leiomyosarcomas, is also described in this paper. The presented case showed that diagnosis and treatment of women with uterine tumors should be individualized as in the same case an extremely rare cancer type can be present which, consequently, changes the treatment regimen and prognosis. Termedia Publishing House 2017-04-26 2017-03 /pmc/articles/PMC5437056/ /pubmed/28546804 http://dx.doi.org/10.5114/pm.2017.67367 Text en Copyright: © 2017 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Case Report
Dudzik, Kamila
Krzysteczko, Agnieszka
Kolny, Leon
Bąk, Agnieszka
Stawicka-Ociepka, Ewelina
Nowosielski, Krzysztof
Synchronous uterine adenocarcinoma and leiomyosarcoma – a case study
title Synchronous uterine adenocarcinoma and leiomyosarcoma – a case study
title_full Synchronous uterine adenocarcinoma and leiomyosarcoma – a case study
title_fullStr Synchronous uterine adenocarcinoma and leiomyosarcoma – a case study
title_full_unstemmed Synchronous uterine adenocarcinoma and leiomyosarcoma – a case study
title_short Synchronous uterine adenocarcinoma and leiomyosarcoma – a case study
title_sort synchronous uterine adenocarcinoma and leiomyosarcoma – a case study
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437056/
https://www.ncbi.nlm.nih.gov/pubmed/28546804
http://dx.doi.org/10.5114/pm.2017.67367
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