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Primary ovarian insufficiency in adolescents: a case series
BACKGROUND: Primary ovarian insufficiency (POI) is characterized by 4 to 6 months of amenorrhea and elevated serum FSH and LH in females less than 40 years. Ovarian insufficiency is uncommon in pediatrics and typically results from a chromosomal abnormality or treatment for malignancy. Idiopathic PO...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433018/ https://www.ncbi.nlm.nih.gov/pubmed/25983758 http://dx.doi.org/10.1186/s13633-015-0009-z |
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author | Pederson, Julia Kumar, Rajiv B Adams Hillard, Paula J Bachrach, Laura K |
author_facet | Pederson, Julia Kumar, Rajiv B Adams Hillard, Paula J Bachrach, Laura K |
author_sort | Pederson, Julia |
collection | PubMed |
description | BACKGROUND: Primary ovarian insufficiency (POI) is characterized by 4 to 6 months of amenorrhea and elevated serum FSH and LH in females less than 40 years. Ovarian insufficiency is uncommon in pediatrics and typically results from a chromosomal abnormality or treatment for malignancy. Idiopathic POI in which no apparent precipitant is identified is even rarer. After encountering three teens with idiopathic POI in recent months, we utilized an informatics-enabled search of the electronic medical records from our hospital to identify all cases of idiopathic POI presenting from 1998–2013. CASES PRESENTATION: 15 girls (ages 14.4 to 17.9 years) met criteria for idiopathic POI. At diagnosis, breast development ranged from Tanner stage 1 to 5; 6 of 15 patients had secondary amenorrhea. All patients presented in the past 11 years and 13 of 15 in the past 5 years. CONCLUSIONS: In this first case series of POI from the United States, we observed a clustering at our institution in recent years. If an increased incidence of idiopathic POI is identified at other institutions, further investigation into potential environmental and genetic precipitants is warranted. |
format | Online Article Text |
id | pubmed-4433018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44330182015-05-16 Primary ovarian insufficiency in adolescents: a case series Pederson, Julia Kumar, Rajiv B Adams Hillard, Paula J Bachrach, Laura K Int J Pediatr Endocrinol Case Report BACKGROUND: Primary ovarian insufficiency (POI) is characterized by 4 to 6 months of amenorrhea and elevated serum FSH and LH in females less than 40 years. Ovarian insufficiency is uncommon in pediatrics and typically results from a chromosomal abnormality or treatment for malignancy. Idiopathic POI in which no apparent precipitant is identified is even rarer. After encountering three teens with idiopathic POI in recent months, we utilized an informatics-enabled search of the electronic medical records from our hospital to identify all cases of idiopathic POI presenting from 1998–2013. CASES PRESENTATION: 15 girls (ages 14.4 to 17.9 years) met criteria for idiopathic POI. At diagnosis, breast development ranged from Tanner stage 1 to 5; 6 of 15 patients had secondary amenorrhea. All patients presented in the past 11 years and 13 of 15 in the past 5 years. CONCLUSIONS: In this first case series of POI from the United States, we observed a clustering at our institution in recent years. If an increased incidence of idiopathic POI is identified at other institutions, further investigation into potential environmental and genetic precipitants is warranted. BioMed Central 2015-05-15 2015 /pmc/articles/PMC4433018/ /pubmed/25983758 http://dx.doi.org/10.1186/s13633-015-0009-z Text en © Pederson et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Pederson, Julia Kumar, Rajiv B Adams Hillard, Paula J Bachrach, Laura K Primary ovarian insufficiency in adolescents: a case series |
title | Primary ovarian insufficiency in adolescents: a case series |
title_full | Primary ovarian insufficiency in adolescents: a case series |
title_fullStr | Primary ovarian insufficiency in adolescents: a case series |
title_full_unstemmed | Primary ovarian insufficiency in adolescents: a case series |
title_short | Primary ovarian insufficiency in adolescents: a case series |
title_sort | primary ovarian insufficiency in adolescents: a case series |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433018/ https://www.ncbi.nlm.nih.gov/pubmed/25983758 http://dx.doi.org/10.1186/s13633-015-0009-z |
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