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A Young Iranian Woman with Pure Primary Ovarian Neuroendocrine Tumor: A Case Report

Pure ovarian neuroendocrine tumors are very rare. Herein, we present a young Iranian woman with a pure primary ovarian neuroendocrine tumor. A 26-year-old female presented with chronic abdominal pain and progressive constipation and was referred to the emergency room. Imaging findings confirmed a ma...

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Autores principales: Samiee-Rad, Fatemeh, Ghaebi, Mahdi, Bajelan, Arezoo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Society of Pathology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508533/
https://www.ncbi.nlm.nih.gov/pubmed/36247498
http://dx.doi.org/10.30699/IJP.2022.542788.2766
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author Samiee-Rad, Fatemeh
Ghaebi, Mahdi
Bajelan, Arezoo
author_facet Samiee-Rad, Fatemeh
Ghaebi, Mahdi
Bajelan, Arezoo
author_sort Samiee-Rad, Fatemeh
collection PubMed
description Pure ovarian neuroendocrine tumors are very rare. Herein, we present a young Iranian woman with a pure primary ovarian neuroendocrine tumor. A 26-year-old female presented with chronic abdominal pain and progressive constipation and was referred to the emergency room. Imaging findings confirmed a mass in the right adnexa. Following the resectional surgery of the ovarian mass, histopathological and immunohistochemistry results disclosed a mixed type of primary ovarian neuroendocrine tumor. The patient did not experience tumor recurrence afterward. Due to the rarity and low prevalence of primary pure ovarian neuroendocrine tumors, the histopathologic diagnosis should be confirmed by an immunohistochemistry study.
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spelling pubmed-95085332022-10-13 A Young Iranian Woman with Pure Primary Ovarian Neuroendocrine Tumor: A Case Report Samiee-Rad, Fatemeh Ghaebi, Mahdi Bajelan, Arezoo Iran J Pathol Case Report Pure ovarian neuroendocrine tumors are very rare. Herein, we present a young Iranian woman with a pure primary ovarian neuroendocrine tumor. A 26-year-old female presented with chronic abdominal pain and progressive constipation and was referred to the emergency room. Imaging findings confirmed a mass in the right adnexa. Following the resectional surgery of the ovarian mass, histopathological and immunohistochemistry results disclosed a mixed type of primary ovarian neuroendocrine tumor. The patient did not experience tumor recurrence afterward. Due to the rarity and low prevalence of primary pure ovarian neuroendocrine tumors, the histopathologic diagnosis should be confirmed by an immunohistochemistry study. Iranian Society of Pathology 2022 2021-08-14 /pmc/articles/PMC9508533/ /pubmed/36247498 http://dx.doi.org/10.30699/IJP.2022.542788.2766 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution- 4.0 International License which permits Share, copy and redistribution of the material in any medium or format or adapt, remix, transform, and build upon the material for any purpose, even commercially.https://creativecommons.org/licenses/by/4.0/
spellingShingle Case Report
Samiee-Rad, Fatemeh
Ghaebi, Mahdi
Bajelan, Arezoo
A Young Iranian Woman with Pure Primary Ovarian Neuroendocrine Tumor: A Case Report
title A Young Iranian Woman with Pure Primary Ovarian Neuroendocrine Tumor: A Case Report
title_full A Young Iranian Woman with Pure Primary Ovarian Neuroendocrine Tumor: A Case Report
title_fullStr A Young Iranian Woman with Pure Primary Ovarian Neuroendocrine Tumor: A Case Report
title_full_unstemmed A Young Iranian Woman with Pure Primary Ovarian Neuroendocrine Tumor: A Case Report
title_short A Young Iranian Woman with Pure Primary Ovarian Neuroendocrine Tumor: A Case Report
title_sort young iranian woman with pure primary ovarian neuroendocrine tumor: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508533/
https://www.ncbi.nlm.nih.gov/pubmed/36247498
http://dx.doi.org/10.30699/IJP.2022.542788.2766
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