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Premature Menarche Associated with Primary Hypothyroidism in a 5.5-Year-Old Girl
Children with hypothyroidism generally have delayed pubertal development. Rare association with precocious puberty may occur especially in long standing untreated patients. The cardinal features of hypothyroidism induced pseudo precocious pubertal development include thelarche, galactorrhea and mena...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420754/ https://www.ncbi.nlm.nih.gov/pubmed/22937289 http://dx.doi.org/10.1155/2011/678305 |
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author | Sharma, Dhrubajyoti Dayal, Devi Gupta, Anju Saxena, Akshay |
author_facet | Sharma, Dhrubajyoti Dayal, Devi Gupta, Anju Saxena, Akshay |
author_sort | Sharma, Dhrubajyoti |
collection | PubMed |
description | Children with hypothyroidism generally have delayed pubertal development. Rare association with precocious puberty may occur especially in long standing untreated patients. The cardinal features of hypothyroidism induced pseudo precocious pubertal development include thelarche, galactorrhea and menarche. Other characteristics features are an absence of sexual hair and retardation of linear growth. Its manifestation as isolated menarche has been rarely reported. Recently, a five and half year old girl presented to us with history of one episode of vaginal bleeding. A pelvic ultrasonogram revealed multiple cysts in both ovaries and subsequent investigations led to a diagnosis of autoimmune hypothyroidism. |
format | Online Article Text |
id | pubmed-3420754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-34207542012-08-30 Premature Menarche Associated with Primary Hypothyroidism in a 5.5-Year-Old Girl Sharma, Dhrubajyoti Dayal, Devi Gupta, Anju Saxena, Akshay Case Rep Endocrinol Case Report Children with hypothyroidism generally have delayed pubertal development. Rare association with precocious puberty may occur especially in long standing untreated patients. The cardinal features of hypothyroidism induced pseudo precocious pubertal development include thelarche, galactorrhea and menarche. Other characteristics features are an absence of sexual hair and retardation of linear growth. Its manifestation as isolated menarche has been rarely reported. Recently, a five and half year old girl presented to us with history of one episode of vaginal bleeding. A pelvic ultrasonogram revealed multiple cysts in both ovaries and subsequent investigations led to a diagnosis of autoimmune hypothyroidism. Hindawi Publishing Corporation 2011 2011-08-23 /pmc/articles/PMC3420754/ /pubmed/22937289 http://dx.doi.org/10.1155/2011/678305 Text en Copyright © 2011 Dhrubajyoti Sharma et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under 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 Sharma, Dhrubajyoti Dayal, Devi Gupta, Anju Saxena, Akshay Premature Menarche Associated with Primary Hypothyroidism in a 5.5-Year-Old Girl |
title | Premature Menarche Associated with Primary Hypothyroidism in a 5.5-Year-Old Girl |
title_full | Premature Menarche Associated with Primary Hypothyroidism in a 5.5-Year-Old Girl |
title_fullStr | Premature Menarche Associated with Primary Hypothyroidism in a 5.5-Year-Old Girl |
title_full_unstemmed | Premature Menarche Associated with Primary Hypothyroidism in a 5.5-Year-Old Girl |
title_short | Premature Menarche Associated with Primary Hypothyroidism in a 5.5-Year-Old Girl |
title_sort | premature menarche associated with primary hypothyroidism in a 5.5-year-old girl |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420754/ https://www.ncbi.nlm.nih.gov/pubmed/22937289 http://dx.doi.org/10.1155/2011/678305 |
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