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Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report
Swyer syndrome is a 46, XY karyotype, with pure gonadal dysgenesis and primary amenorrhea. These females have primordial Mullerian structures and seek medical attention as they experience primary amenorrhea. Here, we report a 15‐year‐old girl, diagnosed as Swyer syndrome associated with left ovarian...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280751/ https://www.ncbi.nlm.nih.gov/pubmed/35846908 http://dx.doi.org/10.1002/ccr3.6083 |
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author | Ashraf Ganjooei, Tahereh Pirastehfar, Zanbagh Mosallanejad, Asieh Raoufi, Masoomeh Afshar Moghaddam, Noushin Hashemieh, Mozhgan |
author_facet | Ashraf Ganjooei, Tahereh Pirastehfar, Zanbagh Mosallanejad, Asieh Raoufi, Masoomeh Afshar Moghaddam, Noushin Hashemieh, Mozhgan |
author_sort | Ashraf Ganjooei, Tahereh |
collection | PubMed |
description | Swyer syndrome is a 46, XY karyotype, with pure gonadal dysgenesis and primary amenorrhea. These females have primordial Mullerian structures and seek medical attention as they experience primary amenorrhea. Here, we report a 15‐year‐old girl, diagnosed as Swyer syndrome associated with left ovarian dysgerminoma. |
format | Online Article Text |
id | pubmed-9280751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92807512022-07-15 Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report Ashraf Ganjooei, Tahereh Pirastehfar, Zanbagh Mosallanejad, Asieh Raoufi, Masoomeh Afshar Moghaddam, Noushin Hashemieh, Mozhgan Clin Case Rep Case Report Swyer syndrome is a 46, XY karyotype, with pure gonadal dysgenesis and primary amenorrhea. These females have primordial Mullerian structures and seek medical attention as they experience primary amenorrhea. Here, we report a 15‐year‐old girl, diagnosed as Swyer syndrome associated with left ovarian dysgerminoma. John Wiley and Sons Inc. 2022-07-14 /pmc/articles/PMC9280751/ /pubmed/35846908 http://dx.doi.org/10.1002/ccr3.6083 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Case Report Ashraf Ganjooei, Tahereh Pirastehfar, Zanbagh Mosallanejad, Asieh Raoufi, Masoomeh Afshar Moghaddam, Noushin Hashemieh, Mozhgan Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report |
title | Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report |
title_full | Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report |
title_fullStr | Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report |
title_full_unstemmed | Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report |
title_short | Dysgerminoma in a 15 years old phenotypically female Swyer syndrome with 46, XY pure gonadal dysgenesis: A case report |
title_sort | dysgerminoma in a 15 years old phenotypically female swyer syndrome with 46, xy pure gonadal dysgenesis: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9280751/ https://www.ncbi.nlm.nih.gov/pubmed/35846908 http://dx.doi.org/10.1002/ccr3.6083 |
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