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Resistance to thyroid hormone β in autoimmune thyroid disease: a case report and review of literature
BACKGROUND: Resistance to thyroid hormone beta (RTHβ) results in symptoms of both increased and decreased thyroid hormone action. The effect of thyroid hormone changes in different types of autoimmune thyroid disease (AITD) in RTHβ is dynamic. CASE PRESENTATION: A 25-year-old Asian female had a RTHβ...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288951/ https://www.ncbi.nlm.nih.gov/pubmed/30526530 http://dx.doi.org/10.1186/s12884-018-2110-9 |
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author | Wu, Di Guo, Rui Guo, Huiling Li, Yushu Guan, Haixia Shan, Zhongyan |
author_facet | Wu, Di Guo, Rui Guo, Huiling Li, Yushu Guan, Haixia Shan, Zhongyan |
author_sort | Wu, Di |
collection | PubMed |
description | BACKGROUND: Resistance to thyroid hormone beta (RTHβ) results in symptoms of both increased and decreased thyroid hormone action. The effect of thyroid hormone changes in different types of autoimmune thyroid disease (AITD) in RTHβ is dynamic. CASE PRESENTATION: A 25-year-old Asian female had a RTHβ Y321C mutation with Hashimoto’s thyroiditis and type 2 diabetes mellitus. She was followed-up through gestation and two years postpartum, revealing development of postpartum thyroiditis (PPT) with characteristic wide fluctuations in serum thyrotropin levels, and of spontaneous recovery from an episode of transient hypothyroidism. The presence of RTHβ did not prolong thyroiditis duration nor progressed toward permanent hypothyroidism. Prenatal genetic analysis was not performed on the unaffected fetus, and did not result in congenital hypothyroidism, possibly because maternal free thyroxine (FT4) levels were mildly elevated at less than 50% above the reference range in early gestation and gradually decreased to less than 20% after the 28th gestational week. CONCLUSION: In RTHβ patients with autoimmune thyroid disease, episodes of thyroid dysfunction can significantly alter thyrotropin levels. During pregnancy, mildly elevated maternal free thyroxine levels less than 20% above the upper limit may not be harmful to unaffected fetuses. Unnecessary thyroid hormone control and fetal genetic testing was avoided during the gestational period with monthly follow-up. |
format | Online Article Text |
id | pubmed-6288951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62889512018-12-14 Resistance to thyroid hormone β in autoimmune thyroid disease: a case report and review of literature Wu, Di Guo, Rui Guo, Huiling Li, Yushu Guan, Haixia Shan, Zhongyan BMC Pregnancy Childbirth Case Report BACKGROUND: Resistance to thyroid hormone beta (RTHβ) results in symptoms of both increased and decreased thyroid hormone action. The effect of thyroid hormone changes in different types of autoimmune thyroid disease (AITD) in RTHβ is dynamic. CASE PRESENTATION: A 25-year-old Asian female had a RTHβ Y321C mutation with Hashimoto’s thyroiditis and type 2 diabetes mellitus. She was followed-up through gestation and two years postpartum, revealing development of postpartum thyroiditis (PPT) with characteristic wide fluctuations in serum thyrotropin levels, and of spontaneous recovery from an episode of transient hypothyroidism. The presence of RTHβ did not prolong thyroiditis duration nor progressed toward permanent hypothyroidism. Prenatal genetic analysis was not performed on the unaffected fetus, and did not result in congenital hypothyroidism, possibly because maternal free thyroxine (FT4) levels were mildly elevated at less than 50% above the reference range in early gestation and gradually decreased to less than 20% after the 28th gestational week. CONCLUSION: In RTHβ patients with autoimmune thyroid disease, episodes of thyroid dysfunction can significantly alter thyrotropin levels. During pregnancy, mildly elevated maternal free thyroxine levels less than 20% above the upper limit may not be harmful to unaffected fetuses. Unnecessary thyroid hormone control and fetal genetic testing was avoided during the gestational period with monthly follow-up. BioMed Central 2018-12-03 /pmc/articles/PMC6288951/ /pubmed/30526530 http://dx.doi.org/10.1186/s12884-018-2110-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Wu, Di Guo, Rui Guo, Huiling Li, Yushu Guan, Haixia Shan, Zhongyan Resistance to thyroid hormone β in autoimmune thyroid disease: a case report and review of literature |
title | Resistance to thyroid hormone β in autoimmune thyroid disease: a case report and review of literature |
title_full | Resistance to thyroid hormone β in autoimmune thyroid disease: a case report and review of literature |
title_fullStr | Resistance to thyroid hormone β in autoimmune thyroid disease: a case report and review of literature |
title_full_unstemmed | Resistance to thyroid hormone β in autoimmune thyroid disease: a case report and review of literature |
title_short | Resistance to thyroid hormone β in autoimmune thyroid disease: a case report and review of literature |
title_sort | resistance to thyroid hormone β in autoimmune thyroid disease: a case report and review of literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288951/ https://www.ncbi.nlm.nih.gov/pubmed/30526530 http://dx.doi.org/10.1186/s12884-018-2110-9 |
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