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A Case of a Girl with Arnold-Chiari Type 1 Malformation with Precocious Puberty

A small percentage of individuals have the neurological anomaly of central precocious puberty (CPP). Common neurologic causes of CPP include a tumor or congenital lesions. Although Arnold-Chiari malformation can be caused by congenital or acquired causes, it is unusual in patients with CPP. We prese...

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Detalles Bibliográficos
Autores principales: Kim, Min Sun, Hwang, Pyoung Han, Lee, Dae-Yeol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Family Medicine 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788847/
https://www.ncbi.nlm.nih.gov/pubmed/29383213
http://dx.doi.org/10.4082/kjfm.2018.39.1.54
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author Kim, Min Sun
Hwang, Pyoung Han
Lee, Dae-Yeol
author_facet Kim, Min Sun
Hwang, Pyoung Han
Lee, Dae-Yeol
author_sort Kim, Min Sun
collection PubMed
description A small percentage of individuals have the neurological anomaly of central precocious puberty (CPP). Common neurologic causes of CPP include a tumor or congenital lesions. Although Arnold-Chiari malformation can be caused by congenital or acquired causes, it is unusual in patients with CPP. We present the case of a girl aged 4.5 years who complained of breast budding. Her neurological examination and growth pattern were normal. She had no endocrinological abnormality, except for true precocious puberty. We performed brain magnetic resonance imaging, which showed an Arnold-Chiari type 1 malformation. Currently, this case represents the youngest girl who exhibited both Arnold-Chiari type 1 malformation and precocious puberty. Furthermore, it is likely that there is a meaningful association between the brain lesion and precocious puberty in this case.
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spelling pubmed-57888472018-01-30 A Case of a Girl with Arnold-Chiari Type 1 Malformation with Precocious Puberty Kim, Min Sun Hwang, Pyoung Han Lee, Dae-Yeol Korean J Fam Med Case Report A small percentage of individuals have the neurological anomaly of central precocious puberty (CPP). Common neurologic causes of CPP include a tumor or congenital lesions. Although Arnold-Chiari malformation can be caused by congenital or acquired causes, it is unusual in patients with CPP. We present the case of a girl aged 4.5 years who complained of breast budding. Her neurological examination and growth pattern were normal. She had no endocrinological abnormality, except for true precocious puberty. We performed brain magnetic resonance imaging, which showed an Arnold-Chiari type 1 malformation. Currently, this case represents the youngest girl who exhibited both Arnold-Chiari type 1 malformation and precocious puberty. Furthermore, it is likely that there is a meaningful association between the brain lesion and precocious puberty in this case. The Korean Academy of Family Medicine 2018-01 2018-01-23 /pmc/articles/PMC5788847/ /pubmed/29383213 http://dx.doi.org/10.4082/kjfm.2018.39.1.54 Text en Copyright © 2018 The Korean Academy of Family Medicine http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Kim, Min Sun
Hwang, Pyoung Han
Lee, Dae-Yeol
A Case of a Girl with Arnold-Chiari Type 1 Malformation with Precocious Puberty
title A Case of a Girl with Arnold-Chiari Type 1 Malformation with Precocious Puberty
title_full A Case of a Girl with Arnold-Chiari Type 1 Malformation with Precocious Puberty
title_fullStr A Case of a Girl with Arnold-Chiari Type 1 Malformation with Precocious Puberty
title_full_unstemmed A Case of a Girl with Arnold-Chiari Type 1 Malformation with Precocious Puberty
title_short A Case of a Girl with Arnold-Chiari Type 1 Malformation with Precocious Puberty
title_sort case of a girl with arnold-chiari type 1 malformation with precocious puberty
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5788847/
https://www.ncbi.nlm.nih.gov/pubmed/29383213
http://dx.doi.org/10.4082/kjfm.2018.39.1.54
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