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An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation
46,XY pure gonadal dysgenesis (Swyer syndrome) is characterized by normal female genitalia at birth. It usually first becomes apparent in adolescence with delayed puberty and amenorrhea. Rarely, patients can present with spontaneous breast development and/or menstruation. A fifteen-year-old girl pre...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563191/ https://www.ncbi.nlm.nih.gov/pubmed/26316442 http://dx.doi.org/10.4274/jcrpe.1919 |
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author | Çatlı, Gönül Alparslan, Caner Can, P. Şule Akbay, Sinem Kelekçi, Sefa Atik, Tahir Özyılmaz, Berk Dündar, Bumin N. |
author_facet | Çatlı, Gönül Alparslan, Caner Can, P. Şule Akbay, Sinem Kelekçi, Sefa Atik, Tahir Özyılmaz, Berk Dündar, Bumin N. |
author_sort | Çatlı, Gönül |
collection | PubMed |
description | 46,XY pure gonadal dysgenesis (Swyer syndrome) is characterized by normal female genitalia at birth. It usually first becomes apparent in adolescence with delayed puberty and amenorrhea. Rarely, patients can present with spontaneous breast development and/or menstruation. A fifteen-year-old girl presented to our clinic with the complaint of primary amenorrhea. On physical examination, her external genitals were completely female. Breast development and pubic hair were compatible with Tanner stage V. Hormonal evaluation revealed a hypergonadotropic state despite a normal estrogen level. Chromosome analysis revealed a 46,XY karyotype. Pelvic ultrasonography showed small gonads and a normal sized uterus for age. SRY gene expression was confirmed by multiplex polymerase chain reaction. Direct sequencing on genomic DNA did not reveal a mutation in the SRY, SF1 and WT1 genes. After the diagnosis of Swyer syndrome was made, the patient started to have spontaneous menstrual cycles and therefore failed to attend her follow-up visits. After nine months, the patient underwent diagnostic laparoscopy. Frozen examination of multiple biopsies from gonad tissues revealed gonadoblastoma. With this report, we emphasize the importance of performing karyotype analysis, which is diagnostic for Swyer syndrome, in all cases with primary or secondary amenorrhea even in the presence of normal breast development. We also suggest that normal pubertal development in patients with Swyer syndrome may be associated with the presence of a hormonally active tumor. |
format | Online Article Text |
id | pubmed-4563191 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Galenos Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-45631912015-09-24 An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation Çatlı, Gönül Alparslan, Caner Can, P. Şule Akbay, Sinem Kelekçi, Sefa Atik, Tahir Özyılmaz, Berk Dündar, Bumin N. J Clin Res Pediatr Endocrinol Case Report 46,XY pure gonadal dysgenesis (Swyer syndrome) is characterized by normal female genitalia at birth. It usually first becomes apparent in adolescence with delayed puberty and amenorrhea. Rarely, patients can present with spontaneous breast development and/or menstruation. A fifteen-year-old girl presented to our clinic with the complaint of primary amenorrhea. On physical examination, her external genitals were completely female. Breast development and pubic hair were compatible with Tanner stage V. Hormonal evaluation revealed a hypergonadotropic state despite a normal estrogen level. Chromosome analysis revealed a 46,XY karyotype. Pelvic ultrasonography showed small gonads and a normal sized uterus for age. SRY gene expression was confirmed by multiplex polymerase chain reaction. Direct sequencing on genomic DNA did not reveal a mutation in the SRY, SF1 and WT1 genes. After the diagnosis of Swyer syndrome was made, the patient started to have spontaneous menstrual cycles and therefore failed to attend her follow-up visits. After nine months, the patient underwent diagnostic laparoscopy. Frozen examination of multiple biopsies from gonad tissues revealed gonadoblastoma. With this report, we emphasize the importance of performing karyotype analysis, which is diagnostic for Swyer syndrome, in all cases with primary or secondary amenorrhea even in the presence of normal breast development. We also suggest that normal pubertal development in patients with Swyer syndrome may be associated with the presence of a hormonally active tumor. Galenos Publishing 2015-06 2015-06-03 /pmc/articles/PMC4563191/ /pubmed/26316442 http://dx.doi.org/10.4274/jcrpe.1919 Text en © Journal of Clinical Research in Pediatric Endocrinology, Published by Galenos Publishing. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Çatlı, Gönül Alparslan, Caner Can, P. Şule Akbay, Sinem Kelekçi, Sefa Atik, Tahir Özyılmaz, Berk Dündar, Bumin N. An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation |
title | An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation |
title_full | An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation |
title_fullStr | An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation |
title_full_unstemmed | An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation |
title_short | An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation |
title_sort | unusual presentation of 46,xy pure gonadal dysgenesis: spontaneous breast development and menstruation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563191/ https://www.ncbi.nlm.nih.gov/pubmed/26316442 http://dx.doi.org/10.4274/jcrpe.1919 |
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