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Serous Cystadenoma with Ectopic Adrenal Cell Rest of Ovary: A Rare Case Report

Ectopic adrenal tissue is an uncommon entity in females. It is usually seen in male children, and the commonly involved sites are the kidney, retroperitoneum, spermatic cord, and paratesticular region. The ectopic adrenal gland in adults has been described in few studies only. Ectopic adrenal tissue...

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Autores principales: Singh, Yasmeen, Bharti, Jyotsna Naresh, Vishnoi, Jeewan Ram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266566/
https://www.ncbi.nlm.nih.gov/pubmed/37324793
http://dx.doi.org/10.4103/jmh.jmh_156_22
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author Singh, Yasmeen
Bharti, Jyotsna Naresh
Vishnoi, Jeewan Ram
author_facet Singh, Yasmeen
Bharti, Jyotsna Naresh
Vishnoi, Jeewan Ram
author_sort Singh, Yasmeen
collection PubMed
description Ectopic adrenal tissue is an uncommon entity in females. It is usually seen in male children, and the commonly involved sites are the kidney, retroperitoneum, spermatic cord, and paratesticular region. The ectopic adrenal gland in adults has been described in few studies only. Ectopic adrenal tissue was diagnosed as an incidental finding in histopathological examination of serous cystadenoma of the ovary. A 44-year-old female presented with a complaint of vague abdominal discomfort for the past few months. Ultrasound was suggestive of a left ovarian complex cystic lesion. The histopathological examination revealed serous cystadenoma with ectopic adrenal cell rest. Here, we present this case as it is a rare finding incidentally detected in a patient being operated on for a different pathology.
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spelling pubmed-102665662023-06-15 Serous Cystadenoma with Ectopic Adrenal Cell Rest of Ovary: A Rare Case Report Singh, Yasmeen Bharti, Jyotsna Naresh Vishnoi, Jeewan Ram J Midlife Health Case Report Ectopic adrenal tissue is an uncommon entity in females. It is usually seen in male children, and the commonly involved sites are the kidney, retroperitoneum, spermatic cord, and paratesticular region. The ectopic adrenal gland in adults has been described in few studies only. Ectopic adrenal tissue was diagnosed as an incidental finding in histopathological examination of serous cystadenoma of the ovary. A 44-year-old female presented with a complaint of vague abdominal discomfort for the past few months. Ultrasound was suggestive of a left ovarian complex cystic lesion. The histopathological examination revealed serous cystadenoma with ectopic adrenal cell rest. Here, we present this case as it is a rare finding incidentally detected in a patient being operated on for a different pathology. Wolters Kluwer - Medknow 2022 2023-04-28 /pmc/articles/PMC10266566/ /pubmed/37324793 http://dx.doi.org/10.4103/jmh.jmh_156_22 Text en Copyright: © 2023 Journal of Mid-life Health https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Singh, Yasmeen
Bharti, Jyotsna Naresh
Vishnoi, Jeewan Ram
Serous Cystadenoma with Ectopic Adrenal Cell Rest of Ovary: A Rare Case Report
title Serous Cystadenoma with Ectopic Adrenal Cell Rest of Ovary: A Rare Case Report
title_full Serous Cystadenoma with Ectopic Adrenal Cell Rest of Ovary: A Rare Case Report
title_fullStr Serous Cystadenoma with Ectopic Adrenal Cell Rest of Ovary: A Rare Case Report
title_full_unstemmed Serous Cystadenoma with Ectopic Adrenal Cell Rest of Ovary: A Rare Case Report
title_short Serous Cystadenoma with Ectopic Adrenal Cell Rest of Ovary: A Rare Case Report
title_sort serous cystadenoma with ectopic adrenal cell rest of ovary: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266566/
https://www.ncbi.nlm.nih.gov/pubmed/37324793
http://dx.doi.org/10.4103/jmh.jmh_156_22
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