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An adolescent girl with premature ovarian failure, Graves’ disease, and chronic urticaria: a case report
BACKGROUND: Premature ovarian failure is characterized by amenorrhea, hypoestrogenism, and hypergonadotropinism, and occurs in women under 40 years of age. The prevalence of premature ovarian failure in women younger than 20 years of age is only 0.01%. Immune disorders are one of the causes of prema...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7548041/ https://www.ncbi.nlm.nih.gov/pubmed/33038927 http://dx.doi.org/10.1186/s13256-020-02491-w |
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author | Lin, Danhong Quan, Huibiao Chen, Kaining Lin, Lu Lin, Leweihua Ji, Qun |
author_facet | Lin, Danhong Quan, Huibiao Chen, Kaining Lin, Lu Lin, Leweihua Ji, Qun |
author_sort | Lin, Danhong |
collection | PubMed |
description | BACKGROUND: Premature ovarian failure is characterized by amenorrhea, hypoestrogenism, and hypergonadotropinism, and occurs in women under 40 years of age. The prevalence of premature ovarian failure in women younger than 20 years of age is only 0.01%. Immune disorders are one of the causes of premature ovarian failure. Graves’ disease and chronic urticaria are also associated with immune disorders. CASE PRESENTATION: We report a case of a 15-year-old Han Chinese girl with premature ovarian failure complicated by Graves’ disease and chronic urticaria. She experienced menarche at 13 years of age and presented with amenorrhea after 7 months of irregular menstruation. Laboratory examinations indicated hypoestrogenism and hypergonadotropinism. Ultrasound imaging revealed that her uterus and ovaries were small in size. Gene and antibody tests related to premature ovarian failure returned negative results. Both thyroid peroxidase autoantibody and thyrotropin receptor antibody were positive. After reviewing the literature on the relationship between these three diseases and immune disorders, our patient was diagnosed as having atypical autoimmune polyglandular syndrome. After taking small doses of estrogen for 6 months, the size of her uterus increased, and her psychological anxiety was relieved. CONCLUSIONS: We report a case of an unusual association of premature ovarian failure, Graves’ disease, and chronic urticaria. This case presents an atypical combination of adolescent autoimmune polyglandular syndrome, which is worthy of the attention of clinicians and presents an important lesson for them. Our case highlights that premature ovarian failure in adolescents requires long-term follow-up and medical treatment as well as psychological counselling. |
format | Online Article Text |
id | pubmed-7548041 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-75480412020-10-13 An adolescent girl with premature ovarian failure, Graves’ disease, and chronic urticaria: a case report Lin, Danhong Quan, Huibiao Chen, Kaining Lin, Lu Lin, Leweihua Ji, Qun J Med Case Rep Case Report BACKGROUND: Premature ovarian failure is characterized by amenorrhea, hypoestrogenism, and hypergonadotropinism, and occurs in women under 40 years of age. The prevalence of premature ovarian failure in women younger than 20 years of age is only 0.01%. Immune disorders are one of the causes of premature ovarian failure. Graves’ disease and chronic urticaria are also associated with immune disorders. CASE PRESENTATION: We report a case of a 15-year-old Han Chinese girl with premature ovarian failure complicated by Graves’ disease and chronic urticaria. She experienced menarche at 13 years of age and presented with amenorrhea after 7 months of irregular menstruation. Laboratory examinations indicated hypoestrogenism and hypergonadotropinism. Ultrasound imaging revealed that her uterus and ovaries were small in size. Gene and antibody tests related to premature ovarian failure returned negative results. Both thyroid peroxidase autoantibody and thyrotropin receptor antibody were positive. After reviewing the literature on the relationship between these three diseases and immune disorders, our patient was diagnosed as having atypical autoimmune polyglandular syndrome. After taking small doses of estrogen for 6 months, the size of her uterus increased, and her psychological anxiety was relieved. CONCLUSIONS: We report a case of an unusual association of premature ovarian failure, Graves’ disease, and chronic urticaria. This case presents an atypical combination of adolescent autoimmune polyglandular syndrome, which is worthy of the attention of clinicians and presents an important lesson for them. Our case highlights that premature ovarian failure in adolescents requires long-term follow-up and medical treatment as well as psychological counselling. BioMed Central 2020-10-11 /pmc/articles/PMC7548041/ /pubmed/33038927 http://dx.doi.org/10.1186/s13256-020-02491-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Case Report Lin, Danhong Quan, Huibiao Chen, Kaining Lin, Lu Lin, Leweihua Ji, Qun An adolescent girl with premature ovarian failure, Graves’ disease, and chronic urticaria: a case report |
title | An adolescent girl with premature ovarian failure, Graves’ disease, and chronic urticaria: a case report |
title_full | An adolescent girl with premature ovarian failure, Graves’ disease, and chronic urticaria: a case report |
title_fullStr | An adolescent girl with premature ovarian failure, Graves’ disease, and chronic urticaria: a case report |
title_full_unstemmed | An adolescent girl with premature ovarian failure, Graves’ disease, and chronic urticaria: a case report |
title_short | An adolescent girl with premature ovarian failure, Graves’ disease, and chronic urticaria: a case report |
title_sort | adolescent girl with premature ovarian failure, graves’ disease, and chronic urticaria: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7548041/ https://www.ncbi.nlm.nih.gov/pubmed/33038927 http://dx.doi.org/10.1186/s13256-020-02491-w |
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