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Challenges in diagnosis and treatment: a case report on a mixed malignant Müllerian tumor

Mixed malignant Müllerian tumors (MMMTs) are rare and aggressive neoplasms made up of both carcinomatous and sarcomatous components that primarily appear in the female reproductive tract. The cellular origin of this malignancy has eluded advancements in molecular and immunohistochemical techniques c...

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Detalles Bibliográficos
Autores principales: Saenz, Daniela, Fernández, Jorge D, Cóbar, Juan P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10505514/
https://www.ncbi.nlm.nih.gov/pubmed/37724065
http://dx.doi.org/10.1093/jscr/rjad523
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author Saenz, Daniela
Fernández, Jorge D
Cóbar, Juan P
author_facet Saenz, Daniela
Fernández, Jorge D
Cóbar, Juan P
author_sort Saenz, Daniela
collection PubMed
description Mixed malignant Müllerian tumors (MMMTs) are rare and aggressive neoplasms made up of both carcinomatous and sarcomatous components that primarily appear in the female reproductive tract. The cellular origin of this malignancy has eluded advancements in molecular and immunohistochemical techniques contributing to the limited diagnostic and therapeutic strategies. This case report presents a 41-year-old female with a history of abnormal uterine bleeding and dysmenorrhea who was later diagnosed with an MMMT. This case highlights the importance of considering MMMTs in patients with a long-standing history of abnormal uterine bleeding because the prompt recognition and diagnosis of this condition may lead to an improved overall survival for these patients.
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spelling pubmed-105055142023-09-18 Challenges in diagnosis and treatment: a case report on a mixed malignant Müllerian tumor Saenz, Daniela Fernández, Jorge D Cóbar, Juan P J Surg Case Rep Case Report Mixed malignant Müllerian tumors (MMMTs) are rare and aggressive neoplasms made up of both carcinomatous and sarcomatous components that primarily appear in the female reproductive tract. The cellular origin of this malignancy has eluded advancements in molecular and immunohistochemical techniques contributing to the limited diagnostic and therapeutic strategies. This case report presents a 41-year-old female with a history of abnormal uterine bleeding and dysmenorrhea who was later diagnosed with an MMMT. This case highlights the importance of considering MMMTs in patients with a long-standing history of abnormal uterine bleeding because the prompt recognition and diagnosis of this condition may lead to an improved overall survival for these patients. Oxford University Press 2023-09-16 /pmc/articles/PMC10505514/ /pubmed/37724065 http://dx.doi.org/10.1093/jscr/rjad523 Text en Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2023. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Saenz, Daniela
Fernández, Jorge D
Cóbar, Juan P
Challenges in diagnosis and treatment: a case report on a mixed malignant Müllerian tumor
title Challenges in diagnosis and treatment: a case report on a mixed malignant Müllerian tumor
title_full Challenges in diagnosis and treatment: a case report on a mixed malignant Müllerian tumor
title_fullStr Challenges in diagnosis and treatment: a case report on a mixed malignant Müllerian tumor
title_full_unstemmed Challenges in diagnosis and treatment: a case report on a mixed malignant Müllerian tumor
title_short Challenges in diagnosis and treatment: a case report on a mixed malignant Müllerian tumor
title_sort challenges in diagnosis and treatment: a case report on a mixed malignant müllerian tumor
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10505514/
https://www.ncbi.nlm.nih.gov/pubmed/37724065
http://dx.doi.org/10.1093/jscr/rjad523
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