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Abstract 145: Etiological profile of precocious puberty: A JIPMER experience
Background: Precocious puberty (PP) is defined as the appearance of secondary sexual characteristics before 8 years in girls and 9 years in boys. The data on the etiological spectrum of precocious puberty from India is limited. Here, we present the analysis of retrospective data of children who pres...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067805/ http://dx.doi.org/10.4103/2230-8210.342270 |
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author | Suryadevara, Varun Patel, Deepika Rashmi, K G Sahoo, Jayaprakash Kamalanathan, Sadishkumar Naik, Dukhabandhu |
author_facet | Suryadevara, Varun Patel, Deepika Rashmi, K G Sahoo, Jayaprakash Kamalanathan, Sadishkumar Naik, Dukhabandhu |
author_sort | Suryadevara, Varun |
collection | PubMed |
description | Background: Precocious puberty (PP) is defined as the appearance of secondary sexual characteristics before 8 years in girls and 9 years in boys. The data on the etiological spectrum of precocious puberty from India is limited. Here, we present the analysis of retrospective data of children who presented with PP to the Department of Endocrinology, JIPMER from 2015 to 2021. Aims and Objectives: To describe the etiological profile of children presenting with PP. Results: A total of 26 children (16 girls) presented during this period with PP. 17 children presented with central PP (CPP). The median age of presentation was 6 years (range 2.5-8 years). The most common etiology for CPP was idiopathic CPP [n=7 (females-6)]) followed by congenital adrenal hyperplasia (CAH) with CPP (n=5) and hypothalamic hamartoma (n=3). One child developed CPP after surgery and radiotherapy for astrocytoma and another child developed CPP after surgery for Leydig cell tumour. 13 children had peripheral PP (PPP). The median age of presentation was 5 years (range 0.8-8 years). 2 cases each were due to adrenal neoplasms and gonadal neoplasms. 2 girls were diagnosed with Mccune Albright syndrome. 6 children (2 girls) had poorly controlled CAH with peripheral PP. 4 of them had progressed to central PP after optimising the GC medication. A girl was diagnosed with Van Wyk-Grumbach syndrome. Conclusion: We present here the retrospective data showing the etiological spectrum of precocious puberty from a tertiary medicare centre. The most common cause of CPP was idiopathic CPP whereas the most common cause of peripheral PP was CAH. |
format | Online Article Text |
id | pubmed-9067805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-90678052022-05-05 Abstract 145: Etiological profile of precocious puberty: A JIPMER experience Suryadevara, Varun Patel, Deepika Rashmi, K G Sahoo, Jayaprakash Kamalanathan, Sadishkumar Naik, Dukhabandhu Indian J Endocrinol Metab Abstracts … Esicon 2021 Background: Precocious puberty (PP) is defined as the appearance of secondary sexual characteristics before 8 years in girls and 9 years in boys. The data on the etiological spectrum of precocious puberty from India is limited. Here, we present the analysis of retrospective data of children who presented with PP to the Department of Endocrinology, JIPMER from 2015 to 2021. Aims and Objectives: To describe the etiological profile of children presenting with PP. Results: A total of 26 children (16 girls) presented during this period with PP. 17 children presented with central PP (CPP). The median age of presentation was 6 years (range 2.5-8 years). The most common etiology for CPP was idiopathic CPP [n=7 (females-6)]) followed by congenital adrenal hyperplasia (CAH) with CPP (n=5) and hypothalamic hamartoma (n=3). One child developed CPP after surgery and radiotherapy for astrocytoma and another child developed CPP after surgery for Leydig cell tumour. 13 children had peripheral PP (PPP). The median age of presentation was 5 years (range 0.8-8 years). 2 cases each were due to adrenal neoplasms and gonadal neoplasms. 2 girls were diagnosed with Mccune Albright syndrome. 6 children (2 girls) had poorly controlled CAH with peripheral PP. 4 of them had progressed to central PP after optimising the GC medication. A girl was diagnosed with Van Wyk-Grumbach syndrome. Conclusion: We present here the retrospective data showing the etiological spectrum of precocious puberty from a tertiary medicare centre. The most common cause of CPP was idiopathic CPP whereas the most common cause of peripheral PP was CAH. Wolters Kluwer - Medknow 2022-03 /pmc/articles/PMC9067805/ http://dx.doi.org/10.4103/2230-8210.342270 Text en Copyright: © 2022 Indian Journal of Endocrinology and Metabolism https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Abstracts … Esicon 2021 Suryadevara, Varun Patel, Deepika Rashmi, K G Sahoo, Jayaprakash Kamalanathan, Sadishkumar Naik, Dukhabandhu Abstract 145: Etiological profile of precocious puberty: A JIPMER experience |
title | Abstract 145: Etiological profile of precocious puberty: A JIPMER experience |
title_full | Abstract 145: Etiological profile of precocious puberty: A JIPMER experience |
title_fullStr | Abstract 145: Etiological profile of precocious puberty: A JIPMER experience |
title_full_unstemmed | Abstract 145: Etiological profile of precocious puberty: A JIPMER experience |
title_short | Abstract 145: Etiological profile of precocious puberty: A JIPMER experience |
title_sort | abstract 145: etiological profile of precocious puberty: a jipmer experience |
topic | Abstracts … Esicon 2021 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9067805/ http://dx.doi.org/10.4103/2230-8210.342270 |
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