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Precocious puberty in a child: A rare cause and review of literature
Precocious puberty (PP) in pediatric office practice is challenging as the cause varies from benign to malignant conditions. Adrenocortical tumors are rare in childhood and pseudo-precocious puberty is the most common clinical presentation in children. We report a case of a 5-year-old boy who presen...
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/PMC9810850/ https://www.ncbi.nlm.nih.gov/pubmed/36618181 http://dx.doi.org/10.4103/jfmpc.jfmpc_376_22 |
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author | Saminathan, Thulasiraj Dhivyalakshmi, J Sneha, Latha M. Joseph, Leena D. |
author_facet | Saminathan, Thulasiraj Dhivyalakshmi, J Sneha, Latha M. Joseph, Leena D. |
author_sort | Saminathan, Thulasiraj |
collection | PubMed |
description | Precocious puberty (PP) in pediatric office practice is challenging as the cause varies from benign to malignant conditions. Adrenocortical tumors are rare in childhood and pseudo-precocious puberty is the most common clinical presentation in children. We report a case of a 5-year-old boy who presented with features of abdominal distention and virilization, and his abdominal magnetic resonance imaging (MRI) revealed an adrenal tumor which was confirmed as adrenocortical carcinoma by biopsy. This case report highlights the importance of the awareness among general practioners and pediatricians to rule out adrenocortical tumors while evaluating a child with PP. |
format | Online Article Text |
id | pubmed-9810850 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-98108502023-01-05 Precocious puberty in a child: A rare cause and review of literature Saminathan, Thulasiraj Dhivyalakshmi, J Sneha, Latha M. Joseph, Leena D. J Family Med Prim Care Case Report Precocious puberty (PP) in pediatric office practice is challenging as the cause varies from benign to malignant conditions. Adrenocortical tumors are rare in childhood and pseudo-precocious puberty is the most common clinical presentation in children. We report a case of a 5-year-old boy who presented with features of abdominal distention and virilization, and his abdominal magnetic resonance imaging (MRI) revealed an adrenal tumor which was confirmed as adrenocortical carcinoma by biopsy. This case report highlights the importance of the awareness among general practioners and pediatricians to rule out adrenocortical tumors while evaluating a child with PP. Wolters Kluwer - Medknow 2022-10 2022-10-31 /pmc/articles/PMC9810850/ /pubmed/36618181 http://dx.doi.org/10.4103/jfmpc.jfmpc_376_22 Text en Copyright: © 2022 Journal of Family Medicine and Primary Care 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 | Case Report Saminathan, Thulasiraj Dhivyalakshmi, J Sneha, Latha M. Joseph, Leena D. Precocious puberty in a child: A rare cause and review of literature |
title | Precocious puberty in a child: A rare cause and review of literature |
title_full | Precocious puberty in a child: A rare cause and review of literature |
title_fullStr | Precocious puberty in a child: A rare cause and review of literature |
title_full_unstemmed | Precocious puberty in a child: A rare cause and review of literature |
title_short | Precocious puberty in a child: A rare cause and review of literature |
title_sort | precocious puberty in a child: a rare cause and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810850/ https://www.ncbi.nlm.nih.gov/pubmed/36618181 http://dx.doi.org/10.4103/jfmpc.jfmpc_376_22 |
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