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Characteristics of Pediatric Pheochromocytoma/paraganglioma
The “rule of 10” used to describe pheochromocytoma/paragangliomas (PCC/PGLs) has been challenged. However, recent studies suggested that pediatric PCC/PGLs may follow a pattern. Hence, we reviewed the available literature to verify the same. We searched PubMed, Scopus, ProQuest, and Google Scholar f...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434735/ https://www.ncbi.nlm.nih.gov/pubmed/28553607 http://dx.doi.org/10.4103/ijem.IJEM_558_16 |
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author | Sarathi, Vijaya |
author_facet | Sarathi, Vijaya |
author_sort | Sarathi, Vijaya |
collection | PubMed |
description | The “rule of 10” used to describe pheochromocytoma/paragangliomas (PCC/PGLs) has been challenged. However, recent studies suggested that pediatric PCC/PGLs may follow a pattern. Hence, we reviewed the available literature to verify the same. We searched PubMed, Scopus, ProQuest, and Google Scholar for studies describing the genotype and/or phenotype characteristics of pediatric PCC/PGL cohorts published after 2000 in English language and those with sample size more than 35 were included in this review. Pediatric PCC/PGLs were malignant in 10%, synchronous bilateral in 20%, extra-adrenal in 30%, among which, 30% were extra-abdominal and familial in 40%. PCC/PGL diagnosed during pediatric age recurs in 50% by 30 years of follow-up and 60% cases occur in boys. Seventy percent of children with PCC/PGL are likely to have sustained hypertension. Germline mutations could be identified in 80% of children with PCC/PGL and 90% are secretory. The review concludes that pediatric PCC/PGLs follow a pattern, which we call “10%–90% rule.” This new rule will help easily remember the characteristics of pediatric PCC/PGLs. |
format | Online Article Text |
id | pubmed-5434735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54347352017-05-26 Characteristics of Pediatric Pheochromocytoma/paraganglioma Sarathi, Vijaya Indian J Endocrinol Metab Review Article The “rule of 10” used to describe pheochromocytoma/paragangliomas (PCC/PGLs) has been challenged. However, recent studies suggested that pediatric PCC/PGLs may follow a pattern. Hence, we reviewed the available literature to verify the same. We searched PubMed, Scopus, ProQuest, and Google Scholar for studies describing the genotype and/or phenotype characteristics of pediatric PCC/PGL cohorts published after 2000 in English language and those with sample size more than 35 were included in this review. Pediatric PCC/PGLs were malignant in 10%, synchronous bilateral in 20%, extra-adrenal in 30%, among which, 30% were extra-abdominal and familial in 40%. PCC/PGL diagnosed during pediatric age recurs in 50% by 30 years of follow-up and 60% cases occur in boys. Seventy percent of children with PCC/PGL are likely to have sustained hypertension. Germline mutations could be identified in 80% of children with PCC/PGL and 90% are secretory. The review concludes that pediatric PCC/PGLs follow a pattern, which we call “10%–90% rule.” This new rule will help easily remember the characteristics of pediatric PCC/PGLs. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5434735/ /pubmed/28553607 http://dx.doi.org/10.4103/ijem.IJEM_558_16 Text en Copyright: © 2017 Indian Journal of Endocrinology and Metabolism http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Review Article Sarathi, Vijaya Characteristics of Pediatric Pheochromocytoma/paraganglioma |
title | Characteristics of Pediatric Pheochromocytoma/paraganglioma |
title_full | Characteristics of Pediatric Pheochromocytoma/paraganglioma |
title_fullStr | Characteristics of Pediatric Pheochromocytoma/paraganglioma |
title_full_unstemmed | Characteristics of Pediatric Pheochromocytoma/paraganglioma |
title_short | Characteristics of Pediatric Pheochromocytoma/paraganglioma |
title_sort | characteristics of pediatric pheochromocytoma/paraganglioma |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434735/ https://www.ncbi.nlm.nih.gov/pubmed/28553607 http://dx.doi.org/10.4103/ijem.IJEM_558_16 |
work_keys_str_mv | AT sarathivijaya characteristicsofpediatricpheochromocytomaparaganglioma |