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Pseudo-Meigs syndrome secondary to endodermal sinus tumor

Ovarian tumors are the most common gynecological tumors seen in girls. Approximately 60–70% of them are germ cell tumors. Pseudo-Meigs syndrome is characterized by the presence of pelvic tumoral mass (benign or malign), pleural effusion, and massive acid. If the tumor is removed, acid and hydrothora...

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Autores principales: Ural, Dilan Altintas, Karakaya, Ali Erdal, Guler, Ahmet Gokhan, Acipayam, Can, Kaya, Mustafa Sabih, Karacaoglu, Mehmet Cihan, Kocarslan, Sezen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Health Directorate of Istanbul 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889214/
https://www.ncbi.nlm.nih.gov/pubmed/36530560
http://dx.doi.org/10.14744/nci.2020.45452
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author Ural, Dilan Altintas
Karakaya, Ali Erdal
Guler, Ahmet Gokhan
Acipayam, Can
Kaya, Mustafa Sabih
Karacaoglu, Mehmet Cihan
Kocarslan, Sezen
author_facet Ural, Dilan Altintas
Karakaya, Ali Erdal
Guler, Ahmet Gokhan
Acipayam, Can
Kaya, Mustafa Sabih
Karacaoglu, Mehmet Cihan
Kocarslan, Sezen
author_sort Ural, Dilan Altintas
collection PubMed
description Ovarian tumors are the most common gynecological tumors seen in girls. Approximately 60–70% of them are germ cell tumors. Pseudo-Meigs syndrome is characterized by the presence of pelvic tumoral mass (benign or malign), pleural effusion, and massive acid. If the tumor is removed, acid and hydrothorax disappear. Endodermal sinus (yolk sac) tumor is a very rare cause in the diagnosis of Pseudo-Meigs syndrome, and only a few cases have been reported. This case is one of the rare cases presenting with Pseudo-Meigs syndrome and pathologically diagnosed as yolk sac tumor.
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spelling pubmed-88892142022-12-15 Pseudo-Meigs syndrome secondary to endodermal sinus tumor Ural, Dilan Altintas Karakaya, Ali Erdal Guler, Ahmet Gokhan Acipayam, Can Kaya, Mustafa Sabih Karacaoglu, Mehmet Cihan Kocarslan, Sezen North Clin Istanb Case Report - Pediatrics Ovarian tumors are the most common gynecological tumors seen in girls. Approximately 60–70% of them are germ cell tumors. Pseudo-Meigs syndrome is characterized by the presence of pelvic tumoral mass (benign or malign), pleural effusion, and massive acid. If the tumor is removed, acid and hydrothorax disappear. Endodermal sinus (yolk sac) tumor is a very rare cause in the diagnosis of Pseudo-Meigs syndrome, and only a few cases have been reported. This case is one of the rare cases presenting with Pseudo-Meigs syndrome and pathologically diagnosed as yolk sac tumor. Health Directorate of Istanbul 2022-12-15 /pmc/articles/PMC8889214/ /pubmed/36530560 http://dx.doi.org/10.14744/nci.2020.45452 Text en Copyright © by by Istanbul Provincial Directorate of Health - Available online at www.northclinist.com https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
spellingShingle Case Report - Pediatrics
Ural, Dilan Altintas
Karakaya, Ali Erdal
Guler, Ahmet Gokhan
Acipayam, Can
Kaya, Mustafa Sabih
Karacaoglu, Mehmet Cihan
Kocarslan, Sezen
Pseudo-Meigs syndrome secondary to endodermal sinus tumor
title Pseudo-Meigs syndrome secondary to endodermal sinus tumor
title_full Pseudo-Meigs syndrome secondary to endodermal sinus tumor
title_fullStr Pseudo-Meigs syndrome secondary to endodermal sinus tumor
title_full_unstemmed Pseudo-Meigs syndrome secondary to endodermal sinus tumor
title_short Pseudo-Meigs syndrome secondary to endodermal sinus tumor
title_sort pseudo-meigs syndrome secondary to endodermal sinus tumor
topic Case Report - Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8889214/
https://www.ncbi.nlm.nih.gov/pubmed/36530560
http://dx.doi.org/10.14744/nci.2020.45452
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