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Agenesis and not ectopia is common in North Indian children with thyroid dysgenesis
CONTEXT: Ectopic Thyroid Gland (ETG) is known to be the most common form of thyroid dysgenesis in children with permanent congenital hypothyroidism (CH). Recent reports indicate that agenesis or hypoplasia of thyroid gland may be commoner as compared to ETG in thyroid dysgenesis (TD). There is limit...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266877/ https://www.ncbi.nlm.nih.gov/pubmed/25538886 http://dx.doi.org/10.4103/2230-8210.145080 |
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author | Dayal, Devi Sindhuja, L. Bhattacharya, Anish Sodhi, Kushaljit Singh Sachdeva, Naresh |
author_facet | Dayal, Devi Sindhuja, L. Bhattacharya, Anish Sodhi, Kushaljit Singh Sachdeva, Naresh |
author_sort | Dayal, Devi |
collection | PubMed |
description | CONTEXT: Ectopic Thyroid Gland (ETG) is known to be the most common form of thyroid dysgenesis in children with permanent congenital hypothyroidism (CH). Recent reports indicate that agenesis or hypoplasia of thyroid gland may be commoner as compared to ETG in thyroid dysgenesis (TD). There is limited information available on the proportion of different variants of TD in Indian children. AIM: To characterize the different TD variants in a cohort of North Indian children with TD. SETTINGS AND DESIGN: Endocrinology Unit of a large Multispecialty Pediatrics Center located in North India. Retrospective review of clinical records of children with CH due to TD diagnosed between April 2004 and March 2014. RESULTS: Diagnoses of TD in 94 children (48 boys and 46 girls) were based on combined scanning with high-resolution ultrasonography, and technetium-99m pertechnetate thyroid scintigraphy. Thyroid agenesis, ectopia and hypoplasia were diagnosed in 74 (78.7%), 14 (14.8%) and 6 (6.4%) patients respectively. The mean initial serum total T4 and thyroid stimulating hormone concentrations at diagnosis were 3.03 ± 2.88 μg/dL (range 0.01–8.9) and 284.52 ± 300.67 mIU/L (range 10.03–1159.0) respectively. Patients with ETG were older at the time of diagnosis as compared to patients with hypoplasia or ectopia. The mean duration of follow-up was 3.7 ± 2.85 years (range 3 months–10 years). CONCLUSIONS: Thyroid agenesis was the most common form of TD in our children with permanent CH. Hypoplasia and ectopia were uncommon. Female preponderance, noted in many previous reports, was not seen in our patients with TD. |
format | Online Article Text |
id | pubmed-4266877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42668772014-12-23 Agenesis and not ectopia is common in North Indian children with thyroid dysgenesis Dayal, Devi Sindhuja, L. Bhattacharya, Anish Sodhi, Kushaljit Singh Sachdeva, Naresh Indian J Endocrinol Metab Brief Communication CONTEXT: Ectopic Thyroid Gland (ETG) is known to be the most common form of thyroid dysgenesis in children with permanent congenital hypothyroidism (CH). Recent reports indicate that agenesis or hypoplasia of thyroid gland may be commoner as compared to ETG in thyroid dysgenesis (TD). There is limited information available on the proportion of different variants of TD in Indian children. AIM: To characterize the different TD variants in a cohort of North Indian children with TD. SETTINGS AND DESIGN: Endocrinology Unit of a large Multispecialty Pediatrics Center located in North India. Retrospective review of clinical records of children with CH due to TD diagnosed between April 2004 and March 2014. RESULTS: Diagnoses of TD in 94 children (48 boys and 46 girls) were based on combined scanning with high-resolution ultrasonography, and technetium-99m pertechnetate thyroid scintigraphy. Thyroid agenesis, ectopia and hypoplasia were diagnosed in 74 (78.7%), 14 (14.8%) and 6 (6.4%) patients respectively. The mean initial serum total T4 and thyroid stimulating hormone concentrations at diagnosis were 3.03 ± 2.88 μg/dL (range 0.01–8.9) and 284.52 ± 300.67 mIU/L (range 10.03–1159.0) respectively. Patients with ETG were older at the time of diagnosis as compared to patients with hypoplasia or ectopia. The mean duration of follow-up was 3.7 ± 2.85 years (range 3 months–10 years). CONCLUSIONS: Thyroid agenesis was the most common form of TD in our children with permanent CH. Hypoplasia and ectopia were uncommon. Female preponderance, noted in many previous reports, was not seen in our patients with TD. Medknow Publications & Media Pvt Ltd 2014-11 /pmc/articles/PMC4266877/ /pubmed/25538886 http://dx.doi.org/10.4103/2230-8210.145080 Text en Copyright: © 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Brief Communication Dayal, Devi Sindhuja, L. Bhattacharya, Anish Sodhi, Kushaljit Singh Sachdeva, Naresh Agenesis and not ectopia is common in North Indian children with thyroid dysgenesis |
title | Agenesis and not ectopia is common in North Indian children with thyroid dysgenesis |
title_full | Agenesis and not ectopia is common in North Indian children with thyroid dysgenesis |
title_fullStr | Agenesis and not ectopia is common in North Indian children with thyroid dysgenesis |
title_full_unstemmed | Agenesis and not ectopia is common in North Indian children with thyroid dysgenesis |
title_short | Agenesis and not ectopia is common in North Indian children with thyroid dysgenesis |
title_sort | agenesis and not ectopia is common in north indian children with thyroid dysgenesis |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266877/ https://www.ncbi.nlm.nih.gov/pubmed/25538886 http://dx.doi.org/10.4103/2230-8210.145080 |
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