46 XY Ovotesticular Disorder: A Rare Case Report with Review of Literature

Ovotesticular disorder represents 10% of cases of disorder of sex development characterized by the presence of both ovarian and testicular tissue in the same individual, with karyotype 46 XY being a rare sex chromosomal abnormality. We report the case of a 16-year-old person, who is reared as female...

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Autores principales: Meenal, Bhati, Meenakshi, Gothwal, Pratibha, Singh, Garima, Yadav, Priyanka, Kathuria, Poonam, Elhence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8384022/
https://www.ncbi.nlm.nih.gov/pubmed/34485063
http://dx.doi.org/10.4103/GMIT.GMIT_107_19
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author Meenal, Bhati
Meenakshi, Gothwal
Pratibha, Singh
Garima, Yadav
Priyanka, Kathuria
Poonam, Elhence
author_facet Meenal, Bhati
Meenakshi, Gothwal
Pratibha, Singh
Garima, Yadav
Priyanka, Kathuria
Poonam, Elhence
author_sort Meenal, Bhati
collection PubMed
description Ovotesticular disorder represents 10% of cases of disorder of sex development characterized by the presence of both ovarian and testicular tissue in the same individual, with karyotype 46 XY being a rare sex chromosomal abnormality. We report the case of a 16-year-old person, who is reared as female, with a complaint of primary amenorrhea along with lack of secondary sexual characteristics, karyotype 46 XY. Prophylactic bilateral gonadectomy was done, and histopathological examination of bilateral gonads revealed ovarian stroma with a few Sertoli cell line tubules suggestive of bilateral ovotestis; hence, we concluded and framed our diagnosis of ovotesticular disorder.
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spelling pubmed-83840222021-09-02 46 XY Ovotesticular Disorder: A Rare Case Report with Review of Literature Meenal, Bhati Meenakshi, Gothwal Pratibha, Singh Garima, Yadav Priyanka, Kathuria Poonam, Elhence Gynecol Minim Invasive Ther Case Report Ovotesticular disorder represents 10% of cases of disorder of sex development characterized by the presence of both ovarian and testicular tissue in the same individual, with karyotype 46 XY being a rare sex chromosomal abnormality. We report the case of a 16-year-old person, who is reared as female, with a complaint of primary amenorrhea along with lack of secondary sexual characteristics, karyotype 46 XY. Prophylactic bilateral gonadectomy was done, and histopathological examination of bilateral gonads revealed ovarian stroma with a few Sertoli cell line tubules suggestive of bilateral ovotestis; hence, we concluded and framed our diagnosis of ovotesticular disorder. Wolters Kluwer - Medknow 2021-08-03 /pmc/articles/PMC8384022/ /pubmed/34485063 http://dx.doi.org/10.4103/GMIT.GMIT_107_19 Text en Copyright: © 2021 Gynecology and Minimally Invasive Therapy 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
Meenal, Bhati
Meenakshi, Gothwal
Pratibha, Singh
Garima, Yadav
Priyanka, Kathuria
Poonam, Elhence
46 XY Ovotesticular Disorder: A Rare Case Report with Review of Literature
title 46 XY Ovotesticular Disorder: A Rare Case Report with Review of Literature
title_full 46 XY Ovotesticular Disorder: A Rare Case Report with Review of Literature
title_fullStr 46 XY Ovotesticular Disorder: A Rare Case Report with Review of Literature
title_full_unstemmed 46 XY Ovotesticular Disorder: A Rare Case Report with Review of Literature
title_short 46 XY Ovotesticular Disorder: A Rare Case Report with Review of Literature
title_sort 46 xy ovotesticular disorder: a rare case report with review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8384022/
https://www.ncbi.nlm.nih.gov/pubmed/34485063
http://dx.doi.org/10.4103/GMIT.GMIT_107_19
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